AU748512B2 - Method for modulating processes mediated by farnesoid activated receptors - Google Patents

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ORIGINAL

o Name and Address of Applicant Actual Inventor(s): Address for Service: Invention Title: The Salk Institute for Biological Studies 10010 North Torrey Pines Road La Jolla California 92037 United States of America Ronald M Evans Barry M Forman Cary A Weinberger Spruson Ferguson St Martins Tower 31 Market Street Sydney NSW 2000 Method for Modulating Processes Mediated by Farnesoid Activated Receptors The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845c METHOD FOR MODULATING PROCESSES MEDIATED BY FARNESOID ACTIVATED RECEPTORS FIELD OF THE INVENTION The present invention relates to intracellular receptors, and ligands therefor. In a particular aspect, the present invention relates to methods for selectively modulating processes mediated by farnesoid activated receptors.

BACKGROUND OF THE INVENTION Molecular cloning studies have demonstrated that receptors for steroids, retinoids, vitamin D and thyroid hormones comprise a superfamily of regulatory proteins that are structurally and functionally related (see Evans, in Science 240:889-895 (1988)). Known as nuclear receptors, these proteins bind to cis-acting elements in the promoters of their target genes and modulate gene expression in response to ligand therefor, such as a hormone.

Nuclear receptors can be classified based on their DNA binding properties (see Evans, supra and Glass, in Endocr. Rev. 15:391-407 (1994)). For example, the glucocorticoid, estrogen, androgen, progestin and mineralocorticoid receptors bind as homodimers to hormone response elements (HREs) organized as inverted repeats (IRs, see Glass, sura) A second class of receptors, including those activated by retinoic acid, thyroid hormone, vitamin D 3 fatty acids/peroxisome proliferators and ecdysone, bind to HREs as heterodimers with a common partner, the retinoid X receptor RXR, also known as the 9-cis retinoic acid receptor; see, for example, Levin et al., in Nature 355:359-361 (1992) and Heyman et al., in Cell 68:397-406 (1992)).

An important advance in the characterization of the nuclear receptor superfamily of regulatory proteins has been the delineation of a growing number of gene products which possess the structural features of nuclear receptors, but which lack known ligands. Accordingly, such receptors are referred to as orphan receptors. The search for activators for orphan receptors has created exciting areas of research on previously unknown signaling pathways (see, for example, Levin et al., (1992), supra and Heyman et al., (1992) supra) Indeed, the ability to identify novel regulatory systems has important implications in physiology as well as human disease and methods for the treatment thereof.

Since receptors have been identified for all known nuclear-acting hormones, a question arises as to the types of molecules that may activate orphan receptors. In view of the fact that products of intermediary metabolism act as transcriptional regulators in bacteria and yeast, such molecules may serve similar functions in higher 20 organisms (see, for example, Tomkins, in Science 189:760- 763 (1975) and O'Malley, in Endocrinology 125:1119-1120 (1989)). For example, a crucial biosynthetic pathway in higher eucaryotes is the mevalonate pathway (see Figure 1), which leads to the synthesis of cholesterol, bile acids, porphyrin, dolichol, ubiquinone, carotenoids, retinoids, vitamin D, steroid hormones and farnesylated proteins.

Farnesyl pyrophosphate (FPP), the metabolically active form of farnesol, represents the last precursor common to all branches of the mevalonate pathway (see Figure As a result, FPP is required for such fundamental biological processes as membrane biosynthesis, hormonal regulation, lipid absorption, glycoprotein synthesis, electron transport and cell growth (see Goldstein and Brown, in Nature 343:425-430 (1990)).

Because of the central role of FPP in the production of numerous biologically important compounds, it is to be expected that its concentration should be closely regulated. This suggests that cells are likely to have developed strategies to sense and respond to changing levels of FPP, or its metabolites. One possible strategy by which cells can accomplish the desired regulation is to utilise a transcription factor whose activity is specifically regulated by a low molecular weight signalling molecule such as an FPP-like molecule. Potential candidates for such means to sense changing levels of FPP, or metabolites thereof, include members of the nuclear receptor superfamily, since these proteins are activated by low molecular weight signalling molecules.

Brief Description of the Invention In accordance with the present invention, we have discovered that an orphan nuclear receptor, referred to as farnesoid activated receptor FAR), is activated by farnesol and related molecules.

T Thus, FAR provides one of the first examples of a vertebrate transcription factor that is regulated by •g an intracellular metabolite. These findings suggest the existence of vertebrate signalling networks that are regulated by products of intermediary metabolism.

According to a first embodiment of the invention there is provided an isolated nucleic acid molecule encoding a mammalian-derived farnesoid activated receptor polypeptide, wherein said polypeptide is a nuclear receptor and is responsive to the presence of farnesoid to regulate the transcription of associated gene(s).

T According to a second embodiment of the invention there is provided an isolated nucleic acid o ,,molecule which encodes a nuclear receptor polypeptide responsive to the presence of farnesoid to regulate the transcription of associated gene(s), wherein said nucleic acid molecule hybridizes to a nucleic acid molecule encoding amino acid residues 1-297 as set forth in SEQ ID NO:2 under the low stringency conditions of 42°C for 24 hours with 0 or 10% formamide, 1X Denhardt's solution, 6X NET, 0.2% SDS, and 100 [Ig/ml denatured salmon sperm DNA, and washed four times for 20 minutes at in 2X SSC, 0.1% SDS.

According to a third embodiment of the invention there is provided an isolated nucleic acid molecule, wherein said nucleic acid molecule encodes a polypeptide comprising amino acid residues 124-189 and amino acids residues 250-469 as set forth in SEQ ID NO:2 or conservative variations thereof, wherein said polypeptide is responsive to the presence of farnesoid to regulate the transcription of associated genes.

According to a fourth embodiment of the invention there is provided an isolated nucleic acid molecule, wherein said nucleic acid molecule encodes amino acid sequence 250-469 as set forth in SEQ ID NO:2 or conservative variations thereof.

1I)\I d.1 I I I1X342Aspcc.do,_,cec According to a fifth embodiment of the invention there is provided an isolated nucleic acid molecule, wherein said nucleic acid encodes amino acid sequence 124-189 as set forth in SEQ ID NO:2 or conservative variations thereof.

According to a sixth embodiment of the invention there is provided a substantially pure farnesoid-activated receptor polypeptide, wherein said polypeptide is responsive to the presence of farnesoid to regulate the transcription of associated gene(s).

According to a seventh embodiment of the invention there is provided a complex comprising the polypeptide in accordance with the sixth embodiment and a homodimeric or heterodimeric partner of the steroid/thyroid hormone superfamily of receptors.

According to an eighth embodiment of the invention there is provided a vertebrate nuclear receptor polypeptide, wherein said polypeptide associates with an IR1 sequence and is encoded by a nucleic acid sequence that hybridizes under low stringency conditions to a nucleic acid sequence encoding the amino acid residues 124 to 189 as set forth in SEQ ID NO:2.

Brief Description of the Figures Figure 1 illustrates the mevalonate pathway and details the relationship between FAR-RXR activators (set off in the figure by enclosure in a box) and the other compounds produced by the mevalonate pathway.

Figure 2 summarizes the relationship among the DNA binding domains of FAR (Cys 124 -Met 189 and other nuclear receptors human peroxisome proliferator activated receptor (PPARao, Fenbank L02932); human retinoid X receptor I IA] XvIA iMI\I It I I:i jX342Aspcc.doc:,_, cc a (RXR, Genbank X52773); human retinoic acid receptor a (RARa, Genbank X06538); human thyroid hormone receptor al (T'Ra, Genbank M24748) human vitamin D receptor (VDR, Genbank J03258); human orphan nuclear receptor (MB67, Genbank L29263); rat orphan nuclear receptor (RLd-1, Genbank U11685); and Drosophila ecdysone receptor (EcR, Genbank M74078). Dendograms were created using the PILEUP program (Genetics Computer Group, version 7.2, University of Wisconsin).

Figure 3 presents an amino acid sequence comparison between rat FAR and Drosophila EcR. Similarity between the DNA binding and ligand binding domains are schematically represented as percent amino acid identity.

Amino acid regions comprising each domain are numbered accordingly.

Figure 4 demonstrates the interaction of FAR and

RXR.

Figures SA, 5B and 5C demonstrate the hormonally controlled activity of the FAR-RXR complex. In Figure 20 the response of FAR alone, RXR alone and FAR RXR to exposure to juvenile hormone III (JH III) is illustrated.

Figure 5B illustrates the response of RXR alone, thyroid hormone receptor (T 3 R) alone, RAR alone and ecdysone receptor ultraspiracle (EcR USP) to exposure to ligands selective for each respective receptor species 100 nM T 3 (L-triiodothyronine), 1 pM trans-RA (all-transretinoic acid) or 100 nM muristerone A, respectively), or to JH III.

Figure SC illustrates the response of FAR alone, RXR alone and FAR RXR to exposure to an FAR ligand (JH III), an RXR ligand (LG69, pentamethyl-5,6,7,8-tetrahydro-2-napthalenyl)-1propenyl)benzoic acid), or a combination of JH III and LG69.

Figure 6A summarizes FAR-RXR activity when exposed to various isoprenoids.

Figure 6B presents a dose-response profile for exposure of FAR-RXR complex to JH III and farnesol.

Figure 7 is an abbreviated genetic map showing the localization of the Fxr gene on mouse Chr DETAILED DESCRIPTION OF THE INVENTION In accordance with the present invention, a novel member of the nuclear receptor superfamily has been identified that forms heterodimers with RXR. The resulting FAR-RXR heterodimer complex is activated by farnesol and related metabolites. This FAR-RXR heterodimer binds to 15 ecdysone-like response elements organized as an inverted repeat spaced by 1 nucleotide (referred to herein as IR1), a property that is unique among vertebrate nuclear receptors.

Thus, as described in greater detail in the Examples which follow, a degenerate 29-mer consensus oligonucleotide corresponding to the highly conserved P-box/DNA recognition helix (TCEGCK(G/V)FF; SEQ ID NO:1) of the nuclear receptor superfamily DNA binding domain (DBD) was used to probe a Xgtll cDNA library derived from mouse hepatoma Hepa-lclc7 mRNA. Four positive cDNAs were identified from a low-stringency screen of two million clones and subjected to nucleotide sequence analysis. In addition to cDNAs for the previously described glucocorticoid and thyroid hormone receptors, two clones encoding novel orphan receptors were obtained. These cDNA clones were about 850 base pairs each and lacked complete coding sequences.

To obtain the complete open reading frame for OR2, a cDNA library from regenerating rat liver was screened. A 2.1 kb cDNA was cloned which encodes a 469 amino acid open reading frame (SEQ ID NO:2). In vitro translation of OR2.8 derived RNA results in a protein with a relative molecular mass of 54,000, close to the predicted Mr of 54,135. The OR2.8 cDNA contains a short interspersed repetitive DNA element (see Sutcliffe et al., in Science 225:1308-1315 (1984)) in the 3' untranslated region, followed by a polyadenylation signal. As described in detail herein, the OR2.8 cDNA encodes a novel member of the nuclear receptor superfamily that is activated by farnesoids. Accordingly, this novel receptor protein is referred to herein as FAR (Farnesoid Activated Receptor) Examination of the amino acid sequence of FAR confirms that it is a member of the nuclear receptor superfamily. The region spanning Cys 24 -Met 289 contains several invariant amino acids, including 4 cysteine residues that are characteristic of the DNA binding domain S. (DBD) of all nuclear hormone receptors. The dendogram in Figure 2 illustrates the relationship of this region to the DBD of other receptors." The FAR DBD is most similar to the DBD of the insect ecdysone receptor (EcR). These receptors share 81% amino acid sequence identity within their DBDs (see Figure The FAR DBD is more distantly related to other members of the nuclear receptor superfamily (see Figure 2).

The carboxy-terminal ligand binding domain (LBD) of nuclear receptors is a complex region encoding subdomains for ligand binding, dimerization and transcriptional activation. Analysis of the carboxy terminal region in FAR (spanning Leu 2 S°-Gln 69 indicates that it possesses only 33% sequence identity (59% similarity) with the corresponding region of the ecdysone receptor (see Figure Within this region, significant similarity is confined to regions involved in receptor dimerization (see Forman and Samuels, in Mol. Endocrinol. 4:1293-1301 (1990)), including the T i subdomain (48% identity), heptad repeats 4-6 (50% identity) and heptad 9 (75% identity). In addition, the last 22 amino acids, which possess transcriptional activation functions in other receptors' 10 (see Danielian et al., in EMBO J. 11:1025-1033 (1992)), are 42% identical among FAR and EcR (see Figure These structural similarities indicate that FAR is a member of the nuclear receptor superfamily with potential functional relatedness to the EcR.

15 As used herein, the phrase amino acid sequence similarity refers to sequences which have amino acid substitutions which do not change the inherent chemical properties of the subject polypeptide. Thus, amino acid *see' sequences wherein an acidic residue is replaced with another acidic residue, or wherein a basic residue is replaced with another basic residue, or wherein a neutral residue is replaced with another neutral residue, retain a high degree of similarity with respect to the original sequence, notwithstanding the fact that the sequences are no longer identical.

The ability to respond to metabolic intermediates distinguishes FAR from other nuclear receptors. FPP, the metabolically active form of farnesol, is a key metabolic precursor in the synthesis of numerous biologically active molecules including proteins (see Figure 1 and Goldstein and Brown, in Nature 343:425-430 (1990).

Transcriptional regulation by intermediary metabolites such as carbohydrates, amino acids and lipids is a common paradigm in bacteria and yeast (see, for example, Sze et al., in Science 258:1143-1145 (1992)). In these systems the metabolite, or a related compound, often serves as an effector in a transcriptionally-regulated feedback loop that maintains appropriate concentrations of the metabolite/effector. The demonstration that FAR-RXR is regulated by farnesoid-related metabolites provides an example of this type of regulation in vertebrates.

Since farnesoid metabolites are synthesized intracellularly, individual cells which express FAR may also be producing the ultimate FAR activator. Other examples of transcriptional signaling by intracellular metabolites include the PPAR, a fatty acid-activated orphan receptor (see Gottlicher et al., in Proc. Natl. Acad. Sci.

USA 89:4653-4657 (1992)) that regulates genes involved in fatty acid metabolism (see Green and Wahli, in Mol. Cell Endocrinol. 100:149-153 (1994)) and adipocyte differentiation (see Tontonoz et al., in Genes Dev. 8:1224- 1234 (1994)). Similarly, the low density lipoprotein oo receptor gene regulator, SREBP-1, is maintained in an 20 inactive form by hydroxycholesterol (see Wang et al., in Cell 77:53-62 (1994)). Together, these systems define a novel paradigm of metabolite-controlled intracellular (metacrine) signaling in vertebrates (see O'Malley, in Endocrinology 125:1119-1120 (1989). Metacrine signaling 25 provides a means to regulate responses to intracellular metabolites in a cell-autonomous fashion. By transducing metabolic cues into genomic responses, FAR, PPAR and SREBP-1 provide examples of a metabolic code proposed by Gordon Tomkins in 1975 (see Tomkins, in Science 189:760-763 (1975)).

Activation of classical nuclear receptors occurs at physiological concentrations of circulating hormones, typically in the nanomolar range. However, the activation of PPAR by naturally occurring fatty acids requires 10-100 yM doses, consistent with the presumed intracellular concentration of these compounds. Physiologic concentrations of farnesoids have been difficult to determine due to their rapid metabolism and potential sequestration by intracellular and extracellular binding proteins.

Intracellular concentrations of farnesoids can be inferred from the Michaelis constant of enzymes that utilize isoprenoid substrates. The K, of farnesyl:proteifn transferases for FPP ranges between 0.5 and 8.5 pM (see Gomez et al., in Biochem. J. 289:25-31 (1993) and Reiss et al., in Cell 62:81-88 (1990)) and half-maximal inhibition of isopentenyl pyrophosphate isomerase occurs with 10 pM FFP (see Rilling and Chayet, In: Sterols and Bile Acids, •"oo eds. Danielsson and Sjovall (Elsevier Science; 1985)).

15 Furthermore, several biological effects of JH III and isoprenoids have been reported to occur in the 10-100 pM concentration range. For example, induction of ornithine decarboxylase by phorbol esters and phytohemagglutinin can be antagonized by 100 pM JH III in bovine lymphocytes (see 20 Kensler et al., in Cancer Res. 38:2896-2899 (1978)).

Similarly, down-regulation of HMG-CoA reductase activity by a mevalonate-derived non-sterol occurs when mevalonate is added to cells at concentrations in excess of 100 pM (see, for example, Brown and Goldstein, in J. Lipid Res. 21:505- 517 (1980), and Nakanishi et al., in J. Biol. Chem.

263:8929-8937 (1988)). Moreover, FAR is expressed in the liver, intestine, adrenal gland and kidney: tissues known to support high flux through the mevalonate pathway. Thus, activation of FAR is likely to occur at appropriate farnesoid concentrations in physiologically relevant tissues.

FPP is known to regulate cell growth by virtue of its ability to alter the intracellular localization of ras and other proteins via covalent farnesylation (Goldstein and Brown, Nature 343:425-430 (1990)). The results presented herein suggest that in addition to this pathway, farnesoids are also capable of promoting biological changes through a novel transcriptional signaling pathway. Indeed, the identification of a farnesoid-dependent transcription factor provides the opportunity to modulate a key pathway responsible for the generation of lipids. Furthermore, the initial identification of a farnesoid-dependent transcription factor suggests that a network of farnesoidresponsive genes exist. Such genes can readily be identified by suitable means having the detailed information concerning FAR provided herein.

In accordance with the present invention, there is provided a method for modulating process(es) mediated by farnesoid activated receptor polypeptides, said method 15 comprising conducting said process(es) in the presence of at least one farnesoid.

Farnesoid activated receptor polypeptides contemplated for use in the practice of the present invention can be characterized by reference to the unique 20 tissue distribution thereof. Thus, expression of FAR polypeptides is restricted to the liver, gut, adrenal gland and kidney, all tissues known to have a significant flux through the mevalonate pathway.

Alternatively, farnesoid activated receptor polypeptides contemplated for use in the practice of the present invention can be characterized by: being responsive to the presence of farnesoid(s) to regulate the transcription of associated gene(s); having a relative molecular mass of about 54,000; and having a DNA binding domain of about 66 amino acids with 9 Cys residues, wherein said DNA binding domain has: about 81 amino acid identity with the DNA binding domain of the Drosophila ecdysone receptor, about 56 amino acid identity with the DNA binding domain of VDR, and about 45 amino acid identity with the DNA binding domain of hGR.

Farnesoid activated receptor polypeptides' contemplated for use in the practice of the present invention can be further characterized by: having a ligand binding domain of about 220 amino acids, wherein said ligand binding domain has: .e about 33 amino acid identity, and 15 about 59 amino acid similarity, with the ligand binding domain of the Drosophila ecdysone receptor, about 32 amino acid identity with the ligand binding domain of VDR, and 20 about 26 amino acid identity with the ligand binding domain of hGR.

Presently preferred farnesoid activated receptor polypeptides contemplated for use in the practice of the present invention can be characterized as having substantially the same amino acid sequence as that shown in SEQ ID NO:2. Especially preferred farnesoid activated receptor polypeptides contemplated for use in the practice of the present invention are those which have the same amino acid sequence as that shown in SEQ ID NO:2.

The phrase "substantially the same" is used herein in reference to amino acid sequences that have slight and non-consequential sequence variations from the actual sequences disclosed herein. Species which are "substantially the same as the reference sequence are considered to be equivalent to the disclosed sequences and as such are within the scope of the appended claims.

Farnesoid compounds contemplated for use in the practice of the present invention include compounds having the structure: R-C(R)q [CR" 2

-CR"

2 -C(R)q CR'q,.]-X or

[CR"

2

-CR"

2 -C(R)q CR'q,.n-X, 0 wherein wherein a a gloo oo each R is independently lower alkyl or alkoxy, each R' is independently selected from hydrogen, lower alkyl or alkoxy, each R" is independently selected from hydrogen, lower alkyl or alkoxy, X is selected from -CH 2 OH, -CH 2 OAc, -COH, or -COMe, n is 2 or 3, each q is independently 1 or 2, each q' is independently 1 or 2, and q and q' are the same.

Exemplary farnesoids contemplated for use in the of the present invention include those wherein: each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -CH 2 OH, n is 2, and each q and q' is 1 the farnesoid molecule is polyunsaturated); each R is methyl, each R' and each R" is hydrogen, X is -COH, n is 2, and each q and q' is 1 the farnesoid molecule is polyunsaturated); the polyene backbone of the farnesoid molecule contains an epoxide functionality, each R is methyl, each R' is hydrogen, each practice R" is hydrogen, X is -CH 2 Me, n is 2, and each q and q' is 1; each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -OAc, n is 2, and each q and q' is 1; each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -CH 2 OH, n is 3, and each q and q' is 1; and the like.

In accordance with another embodiment of the present invention, there is provided a method of testing a compound for its ability to regulate transcriptionactivating effects of a farnesoid activated receptor polypeptide, said method comprising assaying for reporter S..protein when cells containing a farnesoid activated receptor polypeptide and reporter construct are contacted with said compound; wherein said reporter construct comprises: a promoter that is operable in said cell, 20 a hormone response element, and DNA encoding a reporter protein, wherein said reporter protein-encoding DNA segment is operatively linked to said promoter for transcription of said DNA segment, and wherein said promoter is operatively linked to said hormone response element for activation thereof.

The invention will now be described in greater detail by reference to the following non-limiting examples.

Example 1 Cloning of FAR A degenerate 29-mer consensus oligonucleotide TGT GAG GGC TGC AAR GKY TTC TTC AA-3'; SEQ ID NO:3), corresponding to the highly conserved P-box/DNA recognition helix (TCEGCK(G/V)FF; SEQ ID NO:1) of the nuclear receptor superfamily DNA binding domain (DBD) was used to probe a Xgtll mouse hepatoma Hepa-lclc7 cDNA library of 2 X 106 clones under low stringency conditions (see Issemann and Green, in Nature 347:645-650 (1990)) An incomplete 850 bp mouse OR2 cDNA clone was obtained. This clone was used subsequently to screen a regenerated rat liver cDNA library.

A full length clone (referred to as OR2.8) was 15 obtained from this screen and sequenced by the dideoxy sequencing method. The deduced amino acid sequence thereof is presented herein as SEQ ID NO:2.

Example 2 Formation of FAR-RXR complexes 20 In order to explore the functional properties of FAR, the DNA binding properties of this orphan receptor were analyzed.. It has previously been shown that RXR is a common heterodimeric partner required for high affinity DNA binding by several nuclear receptors (see, for example, Hallenbeck et al., in Proc. Natl. Acad. Sci. USA 89:5572- 5576 (1992); Kliewer et al., in Nature 355:446-449 (1992); Leid et al., in Cell 68:377-395 (1992); Marks et al., in EMBO J. 11:1419-1435 (1992); Yu et al., in Cell 67:1251- 1266 (1991); and Zhang et al, in Nature 355:441-446 (1992). Moreover, it has been shown that the DNA and ligand binding activities of the Drosophila ecdysone receptor (EcR) require heterodimer formation with RXR or USP (the Drosophila homologue of RXR; see O'Malley in Endocrinology 125:1119-1120 (1989)). As illustrated in Figure 3, FAR and EcR possess striking similarity within the dimerization subdomain of the ligand binding domain (LBD). Furthermore, FAR is colocalized with sites of RXRa and RXRS expression (see Example 6 below). These observations prompted an investigation as to whether FAR could interact with RXR, or with other members of the nuclear receptor superfamily. To do so, a two-hybrid system modified for use in mammalian cells was employed (see, for example, Nagpal et al., in EMBO J. 12:2349-2360 (1993)).

Thus, CV-1 cells were transiently transfected (as indicated in Figure 4) with cytomegalovirus promoter driven expression vectors containing the yeast GAL4 DNA binding 15 domain (DBD) alone (GAL4 1 147 GAL4 linked to the FAR ligand binding domain (LBD; GAL4-FAR, 184 469 and the 78 amino acid Herpes virus VP16 transactivation domain (VP) linked to the amino terminal end of the LBDs for human RXRce

(VP-RXR

203 462 mouse PPARa (VP-PPAR 1 5 s- 46 VDR (VP-VDR 9 2 4 27

T

3 R) (VP-T 3 R3 173 456 or RARa (VP-RARs 5 6 462 All cells were cotransfected with a luciferase reporter construct containing 4 copies of the yeast GAL4 upstream activating sequence and a 3-galactosidase expression vector as internal control.

Thus, CV-1 cells were grown in DMEM supplemented with 10% AG1-X8 resin-charcoal stripped calf bovine serum, U/ml penicillin G and 50 pg/ml streptomycin sulfate (DMEM-CBS) at 37 0 C in 5% CO 2 One day prior to transfection, cells were plated to 50-80% confluence using phenol-red free DMEM with 10% resin charcoal stripped fetal bovine serum (DMEM-FBS). Cells were transfected (with reporter construct (300 ng/10 5 cells), cytomegalovirus driven receptor (100 ng/10s cells) and -galactosidase expression vectors (500 ng/10 5 cells) as indicated in Figure 4) by lipofection using N-{2-(2,3)-dioleoyloxy)propyl- N,N,N-trimethyl ammonium methyl sulfate} according to the manufacturer's instructions (DOTAP, Boehringer Mannheim).

After 2 hours the liposomes were removed and cells treated for 40 hours with phenol-red free DMEM-FBS containing farnesol as the ligand. Cells were harvested and assayed for luciferase and 0-galactosidase activity. All points were performed in triplicate and varied by less than Experiments were repeated three or more time with similar results. Data points were normalized for differences in transfection efficiency using 0-galactosidase, and plotted as relative activity where the untreated reporter is defined to have an activity of 1 unit.

As seen in Figure 4, neither the GAL4 DBD, nor the GAL4-FAR chimera are capable of stimulating 15 transcription from a reporter construct containing the GAL4 upstream activating sequence. Similarly, a fusion protein containing the Herpes virus VP16 transactivation domain linked to the RXRa-LBD (VP-RXR) is inactive when expressed alone or with the GAL4 DBD. However, when GAL4-FAR and 20 VP-RXR are coexpressed, the reporter is dramatically activated (by about 500-fold), indicating that FAR and RXRa interact efficiently in cells. Using similar VP16-LBD fusion proteins, no interaction could be detected between FAR and receptors for peroxisome proliferators/fatty acids 25 (PPAR) vitamin D 3 (VDR) thyroid hormone (T 3 R) retinoic acid (RAR), or other members of the nuclear receptor superfamily. These data indicate that the LBDs of FAR and RXRa associate in a highly specific fashion.

The only combination resulting in significant activation was GAL4-FAR VP-RXR. As one would expect (based on previous in vitro studies (see Hallenbeck et al., supra and Zhang et al, supra)), VP-PPAR, VP-VDR, VP-T 3 R and VP-PPAR interacted productively with GAL4-RXR, thereby confirming that these VP16 chimeras are functionally expressed.

Example 3 Binding of FAR-RXR complexes to DNA It was next sought to determine the DNA binding properties of the FAR-RXRa complex. Because FAR and EcR share 100% sequence identity in the DNA recognition helix (P-box, Cys" 1 -Lys14), it was examined whether the FAR-RXRa complex could recognize the hsp27 element response element (EcRE; Yao et al., Cell 71:63-72 (1992)). Electrophoretic mobility shift analysis was performed using 3 P]-labeled DNA and in vitro translated FAR and RXRa. Proteins used in electrophoretic mobility shift assays were prepared by translation in a rabbit reticulocyte lysate system (TNT, Promega). Proteins (1pl) were incubated for 20 minutes at room temperature with 100,000 cpm of Klenow-labeled probes 15 in 10 mM Tris pH 8, 100 mM KC1, 6% glycerol, 0.05% 1 mM DTT, 100 ng/il poly dI-dC and then electrophoresed through a 5% polyacrylamide gel in 0.5x TBE. The gel was autoradiographed for 1.5 hours with an intensifying screen.

~Neither FAR nor RXRa alone were capable of high affinity binding to the hsp27-EcRE. However, when mixed, the two proteins bound cooperatively to the hsp27-EcRE (GGTTCA A TGCACT; SEQ ID NO:4). Binding to this element is specific as indicated by the inability of the FAR-RXRa complex to recognize a mutated 11N-hsp27-EcRE (EcREm;CGTTCA 25 A TGCACA; SEQ ID The hsp27-EcRE consists of two imperfect core binding sites arranged as inverted repeats separated by 1 nucleotide (IR1; SEQ ID NO:4). Accordingly, the binding of FAR-RXR was further examined on an idealized IR1 containing two consensus half-sites (AGGTCA A TGACCT; SEQ ID NO:6). The FAR-RXRa complex was also found to bind cooperatively to the idealized IR1, but not to a mutant IR1 containing substitutions within the half-sites (IR1,; AGAACA A TGTTCT; SEQ ID NO:7). Thus, FAR-RXRa binds to ecdysonelike IR1 response elements, and represents the first vertebrate receptor complex to possess this property.

Example 4 Activation by Farnesoids It was next sought to determine whether FAR possessed transcriptional activity that could be hormonally controlled. Based on the identification of an EcRE as a DNA target, a reporter plasmid was constructed containing copies of the hsp27 response element linked to a truncated mouse mammary tumor virus promoter (Yao et al., Nature 366:476-479 (1993)). This reporter was cotransfected into CV-1 cells alone, or with expression vectors for FAR and/or RXRa. Cotransfected cells were treated with a variety of potential ligands and monitored 15 for changes in luciferase activity.

Transient transfections were performed as described in Example 3 using reporter constructs (300-1000 ng/10s cells), cytomegalovirus driven receptor (50 ng/10 cells) and P-galactosidase expression vectors (500 ng/10 20 cells) as indicated in Figures 5A, 5B and Thus, with reference to Figure 5A, CV-1 cells were transiently transfected with hsp27-EcRE x MTV-luciferase alone or with expression vectors for rat FAR and/or human RXRa. Reporter activity was assayed after treating cells with or without 50 pM JH III. Figure illustrates that JH III elicited a dramatic induction fold) of luciferase activity in cells expressing both FAR and RXRr, relative to cells expressing either FAR or RXRc alone. It is of note that JH III failed to activate FAR- RXR complexes using the parental MTV reporter construct, which lacked the EcREs.

In contrast to the demonstrated ability of JH III to activate FAR-RXR complexes (see Figure 5A), JH III fails to activate other nuclear receptors other than FAR, as shown in Figure 5B. Thus, the activity of the following receptor/luciferase reporter pairs were assayed in the presence of 50 pM JH III or the indicated receptor-specific ligand: Drosophila G-EcR+USP/hsp27-EcRE x 5 MTV; human RXRa/CRBPII-TK; human T 3 R/TREp x 2-TK; and human x 2-TK.

As seen in Figure 5C, the FAR-RXR complex is synergistically activated by JH III and LG69 3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-napthalenyl)-1propenyl}benzoic acid). CV-1 cells were transiently transfected as described above with reference to Figure 15 but treated with or without 50 pM JH III, 100 nM LG69 and JH III LG69.

Unexpectedly, JH III (50 pM) elicited a dramatic induction (10-fold) of luciferase activity in cells expressing both FAR and RXRa (Figure 5A). Other potential ligands including steroids, retroretinoids, eicosanoids and bile acids had no effect. JH III appears to be specific for the FAR-RXRa complex since it failed to activate the ecdysone (EcR+USP), 9-cis retinoic acid (RXR), thyroid hormone (T 3 R) or all-trans retinoic acid receptors (RAR) 25 (Figure Although JH III activates FAR-RXRa, it fails to activate either FAR or RXRa alone (Figures 5A and 5B). This is similar to observations with the Drosophila EcR, which requires formation of an EcR/USP or EcR/RXR complex for transcriptional activity (see, for example, Yao et al., in Nature 366:476-479 (1993); Yao et al., in Cell 71:63-72 (1992); and Thomas et al., in Nature 362:471-475 (1993)) EcR itself binds ecdysteroids with low affinity (Yao et al., (1993), supra; high affinity binding and subsequent transcriptional activation requires coexpression of EcR with RXR or USP. Thus, while the EcR/RXR-USP heterodimer is the physiologically active complex, the ability to respond to ecdysone is determined by the EcR component of the complex. Since the EcR-RXR heterodimer is composed of two functional receptors, the complex can be activated independently by ecdysteroids or 9-cis retinoic acid, and synergistically by both ligands (Kensler et al., in Cancer Res. 38:2896-2899 (1978)).

The structural and functional similarities between EcR and FAR prompted an examination of whether the FAR-RXRc complex could also be synergistically activated by JH III and an RXR-specific ligand (such as LG69; see Kurokawa et al., in Nature 371:528-531 (1994)) Thus, 15 using the hsp27 EcRE reporter, the FAR-RXR complex was activated 17-fold by 50 pM JH III, 76-fold by 100 nM LG69 and 212-fold by the combination of JH III and LG69. This synergistic activity required coexpression of FAR with RXRa, RXRE or RXRX. The ability of JH III to synergize 20 with saturating doses of LG69 or 9-cis RA suggests that these two compounds have distinct targets within the FAR- RXR complex. Since LG69 has previously been shown to be an RXR-specific ligand, these results imply that JH III responsiveness is determined by the FAR component of the 25 FAR-RXR complex.

Example Evaluation of Mevalonate Metabolites as FAR Ligands JH III (cis-10,11-epoxy-3,7,11-trimethyl-transtrans-2,6-dodecadienoic acid methyl ester) is a metabolic derivative of farnesyl pyrophosphate (FPP; 3,7,11trimethyl-2,6,10-dodecatrien-l-ol-pyrophosphate (seeFigure 6A) FPP is derived from the mevalonate biosynthetic pathway and is itself a precursor in the synthesis of other biologically active compounds (see Figure 1, and Goldstein and Brown, in Nature 343:425-430 (1990). Accordingly, it was decided to test whether metabolites derived from the mevalonate pathway in mammalian cells could also serve as activators of the FAR-RXRa complex.

Mevalonate can be synthesized de novo from acetyl CoA and is metabolized into farnesyl pyrophosphate

(FPP),

the metabolically active form of farnesol. FPP serves as a key intermediate in that it represents a critical branch' point in the mevalonate pathway. Accordingly, metabolites of FPP contribute to a number of essential cellular processes. The results presented herein indicate that the FAR-RXR nuclear receptor complex responds most efficiently to farnesol and juvenile hormone III. These findings suggest that metabolic intermediates are capable of serving ee 15 as transcriptional regulators in animal cells. Based on the results presented herein, it is likely that the FAR-RXR complex plays a central role in a feedback loop that serves to regulate the synthesis of enzymes within the mevalonate pathway.

C

Thus, CV-1 cells were transiently transfected with expression vectors for rat FAR and human RXRc, as described above in Example 3. Cells were treated with pM concentrations of farnesol and/or farnesol metabolites.

Data is plotted in Figure 6A as fold activation relative to 25 untreated cells. Similar results were obtained with alltrans retinoic acid and mixed isomers of farnesol and farnesoic acid.

Figure 6B presents a dose-response profile for the two most effective activators observed in the evaluation described in Figure 6A, JH III and farnesol. The experiments were performed as described above for Figure 6A, with the concentration of JH III and farnesol (mixed isomers) indicated in the Figure.

Activation required concentrations in the range of 5-50 pM.

Remarkably, farnesol (trans-trans or mixed isomers, 50 M) was observed to be a strong activator of FAR-RXR (see Figure 6A), whereas other farnesoids, such as farnesal, farnesyl acetate and geranylgeraniol, possessed weaker activity. In contrast, little or no activation was seen with 50 pM concentrations of geraniol, farnesoic acid, squalene, methoprene, mevalonate, squalene epoxide, squalene dioxide, lanosterol, 24 25 -epoxycholesterol, pregnenolone, dehydroepiandrosterone, bile acids or 10 jM 25-hydroxycholesterol. Mevalonate (200 jM) displayed weak activity, provided cells were cotransfected with a mevalonate transporter protein (see Kim et al., in J. Biol.

Chem. 267:23223-23121 (1992)).

e Example 6 15 Expression of FAR mRNA One expectation of an intracellular metabolic activator is that it would be synthesized in the same tissues where its receptor is expressed. Accordingly, the expression of FAR in rat tissues was examined by Northern blot analysis. For Northern analysis, polyA' RNA (10 jg) from various rat tissues was electrophoresed through a 1% agarose gel under denaturing conditions and transferred to a filter. The filter was hybridized to the mouse FAR truncated cDNA that was ["P]-labeled by the random primer 25 method (see Mangelsdorf et al., Genes Dev. 6:329-344 (1992); 5 x 108 cpm/pg). This probe corresponds to rat FAR sequences spanning amino acids 1-297 which encode the N-terminus, the DNA binding domain (DBD) and a portion of the ligand binding domain (LBD) of FAR.

Hybridization was performed overnight at 65 0 C in 500 mM sodium phosphate (dibasic:monobasic, 1 mM ethylenediaminetetraacetic acid, 1% bovine serum albumin and 7% sodium dodecyl sulfate. The filter was washed twice in 2X SSC (Ix SSC is 0.15 M NaC1, 0.015 M sodium citrate) at room temperature, twice in 1X SSC at 55 0 C and then autoradiographed with an intensifying screen at -70 0 C for days. In situ hybridizations were performed as described by Bradley et al., in Proc. Natl. Acad. Sci. USA 91:439-443 (1994). Sections were apposed to Kodak X-OMAT film for days, and then coated with nuclear emulsion and exposed for 16 weeks.

A single transcript of 2.3 kb was observed only' in liver and kidney. No significant expression was detected in the brain, heart, lung, skeletal muscle, pancreas, skin, spleen or testis.

.0 00 In situ hybridization/histochemistry was performed to further localize sites of FAR expression.

Antisense cRNA probes from truncated mouse FAR cDNA or 15 full-length mouse RXR3 cDNA were used. The control was a truncated rat glucocorticoid receptor sense cRNA probe.

The control probe revealed near-background hybridization.

FAR transcripts were restricted to the liver, kidney and gut of rat embryonic day 19.5 (E19.5) embryo sections. Near background levels were seen in other tissues and in experiments using a control probe. As one might expect (see Mangelsdorf et al., in Genes Dev. 6:329- 344 (1992)), mRNA for the heterodimerizing partner RXRS is also found in the liver, kidney and gut, as well as other embryonic tissues. FAR expression in the gut is prominent in the intestinal villi. In the E19.5 kidney, expression is heterogeneous, with highest FAR levels confined to the renal tubules. In the adult kidney, high levels of expression of FAR are seen in areas rich in renal tubules: the medullary rays and medullary stripe. FAR expression is also detected in the adrenal cortex of the adult mouse.

Thus, FAR expression is restricted to the liver, gut, adrenal gland and kidney: tissues known to have significant flux through the mevalonate pathway (see, for example, Edmond et al., in Science 193:154-156 (1976); Righetti et al., in J. Biol. Chem. 251:2716-2721 (1976); and Wiley et al., in J. Biol. Chem. 252:548-554 (1977)).

Example 7 FAR Gene Family The chromosomal location of mouse FAR was determined by analysis of 2 multilocus genetic crosses for inheritance of polymorphic FAR gene fragments (see Danciger et al., in Mouse Genome 91:320-322 (1993), and Sunada et al., in J. Biol. Chem. 269:13729-13732 (1994)).

I. Thus, truncated mouse FAR cDNA was used as a probe to analyze 2 multilocus genetic crosses for inheritance of polymorphic Fxr gene fragments: (NFS/N or C58/J x M. m musculus and (NFS/N x M. spretus) x M spretus 15 or C58/J. DNA from the progeny of these crosses have been typed for approximately 700 markers including the Chr markers Pfp (pore forming protein), Tral (tumor rejection antigen gp96), Ifg (interferon Gli (glioma associated oncogene) and Gadl-psl (glutamic acid decarboxylase 1 20 pseudogene).

To the right of the map (Figure 7) are the recombination fractions between adjacent loci; percent recombination and standard errors are shown in parentheses.

Human map locations for the homologues of individual genes are indicated to the left of the map.

To determine whether there may be related genes that comprise aFAR gene family, Southern blot analysis of rat genomic DNA was performed and the patterns obtained under high and low stringency hybridization were compared.

Thus, duplicate samples of Lewis rat DNA (10Ag) were digested with a variety of restriction enzymes and electrophoresed through a 1% agarose gel. DNA was digested with restriction enzyme, transferred to a nitrocellulose filter and then hybridized with the ["P]-labeled mouse FAR truncated cDNA probe under high or low stringency conditions. As one might expect, high stringency conditions revealed a limited number of specific bands for each restriction enzyme. Under low stringency conditions, many additional bands were obtained, suggesting the existence of one or more FAR-related genes in the rat genome. Although further analysis is required to determine whether these related sequences are functionally expressed, these findings raise the possibility that additional farnesoid activated receptors will be identified.

Se e Southern analysis revealed HindIII digested fragments of 7.5 kb, 6.0 kb and 3.0 kb in NFS/N mouse DNA 15 and 25.0, 7.5 and 3.0 kb in M. spretus. Scal digestion produced fragments of 23.1 kb in NFS/N and 28 kb in M.

m.musculus. The inheritance of these fragments demonstrated that Fxr, the gene encoding FAR, is localized near the Tral locus on mouse Chromosome 10 (Figure 7) This map location is within a region of conserved linkage with human chromosome 12q suggesting a possible map location for human Fxr.

While the invention has been described in detail with reference to certain preferred embodiments thereof, it will be understood that modifications and variations are within the spirit and scope of that which is described and claimed.

SEQUENCE LISTING GENERAL INFORMATION: APPLICANT: Evans, Ronald M.

Forman, Barry M.

Weinberger, Cary A.

(ii) TITLE OF INVENTION: METHOD FOR MODULATING PROCESSES MEDIATED BY FARNESOID ACTIVATED RECEPTORS (iii) NUMBER OF SEQUENCES: 7 (iv) CORRESPONDENCE ADDRESS: ADDRESSEE: Pretty, Schroeder, Brueggemann Clark STREET: 444 South Flower Street, Suite 2000 CITY: Los Angeles STATE: CA COUNTRY: USA ZIP: 90071 COMPUTER READABLE FORM: MEDIUM TYPE: Floppy disk COMPUTER: IBM PC compatible 20 OPERATING SYSTEM: PC-DOS/MS-DOS SOFTWARE: PatentIn Release Version #1.25 S0 (vi) CURRENT APPLICATION DATA: APPLICATION NUMBER: FILING DATE:

CLASSIFICATION:

viii) ATTORNEY/AGENT INFORMATION: NAME: Reiter, Stephen E.

REGISTRATION NUMBER: 31,192 REFERENCE/DOCKET NUMBER: P41 9844 (ix) TELECOMMUNICATION INFORMATION: TELEPHONE: 619-546-4737 TELEFAX: .619-546-9392 INFORMATION FOR SEQ ID NO:1: e SEQUENCE CHARACTERISTICS: 35 LENGTH: 9 amino acids TYPE: amino acid TOPOLOGY: linear (ii) MOLECULE TYPE: protein FRAGMENT TYPE: internal (ix) FEATURE: NAME/KEY: Modified-site LOCATION: 7 OTHER INFORMATION: /note= "Xaa at position 7 is either a glycine or valine (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: Thr Cys Glu Gly Cys Lys Xaa Phe Phe 1 INFORMATION FOR SEQ ID NO:2: SEQUENCE CHARACTERISTICS: LENGTH: 469 amino acids TYPE: amino acid TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: Met Asn Leu Ile Gly Pro Ser His Leu Gin Ala Thr Asp Glu Phe Ala 1 5 10 Leu Ser Glu Asn Leu Phe Gly Val Leu Thr Glu His Ala Ala Gly Pro 25 Leu Gly Gin Asn Leu Asp Leu Glu Ser Tyr Ser Pro Tyr Asn Asn Val S: 35 40 Gin Phe Pro Gin Val Gin Pro Gin Ile Ser Ser Ser Ser Tyr Tyr Ser S* 15 50 55 Asn Leu Gly Phe Tyr Pro Gin Gin Pro Glu Asp Trp Tyr Ser Pro Gly 70 75 Leu Tyr Glu Leu Arg Arg Met Pro Thr Glu Ser Val Tyr Gin Gly Glu 90 Thr Glu Val Ser Glu Met Pro Val Thr Lys Lys Pro Arg Met Ala Ala 100 105 110 Ser Ser Ala Gly Arg Ile Lys Gly Asp Glu Leu Cys Val Val Cys Gly 115 120 125 Asp Arg Ala Ser Gly Tyr His Tyr Asn Ala Leu Thr Cys Glu Gly Cys 130 135 140 Lys Gly Phe Phe Arg Arg Ser Ile Thr Lys Asn Ala Val Tyr Lys Cys 145 150 155 160 Lys Asn Gly Gly Asn Cys Val Met Asp Met Tyr Met Arg Arg Lys Cys 165 170 175 Gin Asp Cys Arg Leu Arg Lys Cys Arg Glu Met Gly Met Leu Ala Glu 180 185 190 Cys Leu Leu Thr Glu Ile Gin Cys Lys Ser Lys Arg Leu Arg Lys Asn 195 200 205 Val Lys Gin His Ala Asp Gin Thr Val Asn Glu Asp Ser Glu Gly Arg 210 215 220 Asp Leu Arg Gin Val Thr Ser Thr Thr Lys Leu Cys Arg Glu Lys Thr 225 230 235 240 Glu Leu Thr Val Asp Gin Gin Thr Leu Leu Asp Tyr Ile Met Asp Ser 245 250 255 Tyr Ser Lys Gin Arg Met Pro Gin Glu Ile Thr Asn Lys Ile Leu Lys 260 265 270 Glu Glu Phe Ser Ala Glu Glu Asn Phe Leu Ile Leu Thr Glu Met Ala 275 280 285 28 Thr Ser His Val Gin Ile Leu Val Glu Phe Thr Lys Arg Leu Pro Gly 290 295 300 Phe Gin Thr Leu Asp His Glu Asp Gin Ile Ala Leu Leu Lys Gly Ser 305 310 315 320 Ala Val Glu Ala Met Phe Leu Arg Ser Ala Glu Ile Phe Asn Lys Lys 325 330 335 Leu Leu Pro Asp Thr Gin Thr Cys Trp Lys Lys Glu Phe Glu Arg Ala 340 345 350 Ala Ser Pro Met Arg Tyr Ile Thr Pro Met Phe Ser Phe Tyr Lys Ser 355 360 365 Val Gly Glu Leu Lys Met Thr Gin Glu Glu Tyr Ala Leu Leu Thr Ala 370 375 380 Ile Val Ile Leu Ser Pro Asp Arg Gin Tyr Ile Lys Asp Arg Glu Ala 385 390 395 400 Val Glu Lys Leu Gin Glu Pro Leu Leu Asp Val Leu Gin Lys Leu Cys 405 410 415 Lys Ile Tyr Gin Pro Glu Asn Pro Gin His Phe Ala Cys Leu Leu Gly 420 425 430 Arg Leu Thr Glu Leu Arg Thr Phe Asn His His His Ala Glu Met Leu S. 20 435 440 445 Met Ser Trp Arg Val Asn Asp His Lys Phe Thr Pro Leu Leu Cys Glu 450 455 460 Ile Trp Asp Val Gin 465 INFORMATION FOR SEQ ID NO:3: SEQUENCE CHARACTERISTICS: LENGTH: 29 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: Other nucleic acid; DESCRIPTION: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: ACCTGTGAGG GCTGCAARGK YTTCTTCAA 29 INFORMATION FOR SEQ ID NO:4: SEQUENCE CHARACTERISTICS: LENGTH: 13 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: Other nucleic acid; DESCRIPTION: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: GGTTCAATGC ACT 13 INFORMATION FOR SEQ ID SEQUENCE CHARACTERISTICS: LENGTH: 13 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: Other nucleic acid; DESCRIPTION: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID CGTTCAATGC ACA 13 INFORMATION FOR SEQ ID NO:6: SEQUENCE CHARACTERISTICS: 15 LENGTH: 13 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: Other nucleic acid; 20 DESCRIPTION: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: AGGTCAATGA CCT 13 INFORMATION FOR SEQ ID NO:7: SEQUENCE CHARACTERISTICS: LENGTH: 13 base pairs S9 TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: Other nucleic acid; DESCRIPTION: Oligonucleotide (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: AGAACAATGT TCT 13

Claims (25)

1. An isolated nucleic acid molecule encoding a mammalian-derived farnesoid activated receptor polypeptide, wherein said polypeptide is a nuclear receptor and is responsive to the presence of farnesoid to regulate the transcription of associated gene(s).

2. The nuclear receptor according to claim 1, wherein said polypeptide is characterized by having a ligand binding domain, wherein said ligand binding domain binds farnesoids.

3. The nucleic acid molecule according to claim 1 or 2, wherein said farnesoid activated receptor polypeptide is further characterized by having a relative molecular mass of about 54,000 Daltons.

4. The nucleic acid molecule according to claim 3, wherein said ligand binding domain is about 220 amino acids. The nucleic acid molecule according to claim 1, wherein said nucleic acid molecule S: hybridizes to a nucleic acid molecule encoding amino acid sequence shown in SEQ ID NO:2 under Sthe low stringency conditions of 42°C for 24 hours with 0 or 10% formamide, 1X Denhardt's solution, 6X NET, 0.2% SDS, and 100 ptg/ml denatured salmon sperm DNA, and washed four times for 20 minutes at 25°C in 2X SSC, 0.1% SDS.

6. The nucleic acid molecule according to claim 1, wherein said polypeptide has the same amino acid sequence as that shown in SEQ ID NO:2 or conservative variations thereof.

7. An isolated nucleic acid molecule which encodes a nuclear receptor polypeptide n responsive to the presence of farnesoid to regulate the transcription of associated gene(s), wherein said nucleic acid molecule hybridizes to a nucleic acid molecule encoding amino acid residues 1-297 as set forth in SEQ ID NO:2 under the low stringency conditions of 42°C for 24 hours with 0 or formamide, 1X Denhardt's solution, 6X NET, 0.2% SDS, and 100 ,pg/ml denatured salmon sperm DNA, and washed four times for 20 minutes at 25°C in 2X SSC, 0.1% SDS.

8. An isolated nucleic acid molecule comprising nucleotides encoding a DNA binding domain comprising about 66 amino acids and 9 Cys residues, wherein said nucleic acid molecule hybridizes to a nucleic acid molecule encoding amino acid sequence 250-469 as set forth in SEQ ID NO:2 under the low stringency conditions of 42 0 C for 24 hours with 0 or 10% formamide, 1X Denhardt's solution, 6X NET, 0.2% SDS, and 100 p.g/ml denatured salmon sperm DNA, and Swashed four times for 20 minutes at 25°C in 2X SSC, 0.1% SDS.

9. An isolated nucleic acid molecule, wherein said nucleic acid molecule encodes a polypeptide comprising amino acid residues 124-189 and amino acids residues 250-469 as set forth in SEQ ID NO:2 or conservative variations thereof, wherein said polypeptide is responsive to the presence of farnesoid to regulate the transcription of associated genes. I] )aY L I. I It Fr:I: ION.;42iAsIccIoc:!gcc An isolated nucleic acid molecule, wherein said nucleic acid molecule encodes amino acid sequence 250-469 as set forth in SEQ ID NO:2 or conservative variations thereof.

11. An isolated nucleic acid molecule, wherein said nucleic acid encodes amino acid sequence 124-189 as set forth in SEQ ID NO:2 or conservative variations thereof.

12. A substantially pure farnesoid-activated receptor polypeptide, wherein said polypeptide is responsive to the presence of farnesoid to regulate the transcription of associated gene(s).

13. A polypeptide according to claim 12, wherein said polypeptide is characterized by: having a relative molecular mass of about 54,000 daltons; and having a DNA binding domain of about 66 amino acids with 9 cys residues, ji( wherein said DNA binding domain is encoded by a nucleic acid sequence that hybridizes under low stringency conditions to a nucleic acid molecule encoding amino acid residues 124 to 189 as set forth in SEQ ID NO:2.

14. A polypeptide according to claim 13, wherein said polypeptide is further characterized by having a ligand binding domain of about 220 amino acids.

15. A polypeptide according to claim 12, wherein said polypeptide is encoded by a nucleic acid sequence that hybridizes under low stringency conditions to a nucleic acid sequence encoding the amino acid residues 250 to 469 as set forth in SEQ ID NO:2.

16. A polypeptide according to claim 12, wherein said polypeptide is encoded by DNA that hybridizes under low stringency conditions to DNA encoding the amino acid sequence shown in SEQ ID NO:2.

17. A polypeptide according to claim 16, wherein said polypeptide has the same amino acid sequence as that shown in SEQ ID NO:2 or conservative variations thereof.

18. A polypeptide according to claim 12, wherein said farnesoid comprises a substituted polyene backbone having the structure: R C(R)q- C [CR" 2 -C R" 2 C(R)q- C R'q']n X or R-C(R)-C [CR" 2 -CR" 2 C R'q]n X 0 wherein each R is independently lower alkyl or alkoxy, *1 each R' is independently hydrogen, lower alkyl or alkoxy, each R" is independently hydrogen, lower alkyl or alkoxy, X is -CH20H, -CH20Ac, -CO 2 H, or -CO2Me, n is 2 or 3, each q is independently 1 or 2, I .ib\I .1 I 10X342Aspc.doc:gcc 32 each q' is independently 1 or 2, and q and q' are the same.

19. A polypeptide according to claim 18 wherein each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -CH 2 0H, n is 2, and each q and q' is 1. A polypeptide according to claim 18 wherein each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -CO 2 H, n is 2, and each q and q' is 1.

21. A polypeptide according to claim 18 wherein the polyene backbone of said farnesoid contains an epoxide functionality, each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -CH 2 Me, n is 2, and each q and q' is 1.

22. A polypeptide according to claim 18 wherein each R is methyl, each R' is hydrogen, each SR" is hydrogen, X is -OAc, n is 2, and each q and q' is 1.

23. A polypeptide according to claim 18 wherein each R is methyl, each R' is hydrogen, each R" is hydrogen, X is -CH 2 0H, n is 3, and each q and q' is 1.

24. A complex comprising the polypeptide of claim 12 and a homodimeric or heterodimeric 'Was •partner of the steroid/thyroid hormone superfamily of receptors. i 25. A complex according to claim 24 wherein said homodimeric or heterodimeric partner of the steroid/thyroid hormone superfamily of receptors is thyroid hormone receptor, retinoic acid receptor, retinoid X receptor or ultraspiracle.

26. A vertebrate nuclear receptor polypeptide, wherein said polypeptide associates with an *IR1 sequence and is encoded by a nucleic acid sequence that hybridizes under low stringency an conditions to a nucleic acid sequence encoding the amino acid residues 124 to 189 as set forth in SEQ ID NO:2.

27. An isolated nucleic acid molecule encoding a mammalian-derived farnesoid activated receptor polypeptide, substantially as hereinbefore described with reference to any one of the *co* examples.

28. A substantially pure farnesoid-activated receptor polypeptide, substantially as hereinbefore described with reference to any one of the examples.

29. A complex comprising the peptide of claim 28, and a homodimeric or heterodimeric partner of the steroid/thyroid hormone superfamily of receptors Dated 4 July, 2000 The Salk Institute for Biological Studies Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON I MYi I. i 11111:108342 As flic d ocg cc