CA2072644A1 - Beta retinoic acid response elements compositions and assays - Google Patents

Abstract

The present invention provides transcriptional control regions, expression vectors comprising said regions, mammalian cells transformed to transcribe and express genes from said vectors, and various methods of assaying compounds for hormone agonist or antagonist activity, all based on discovery of response elements of the .beta.-retinoic acid receptor and of the activation of said response elements in all mammalian cells without need to transform the cells to express the receptor independently of endogenous expression thereof.

Description

~ ~VO9l/07~88 2 ~ 7 ~ 6 ~ ~ Pcr/-s90/066z6 BETA RETINOIc ACID RESPONSE ELEMENTS
_OMPOSITIONS AND ASSAYS

The invention described and claimed herein was made with support fro,m the Vnited States National Institutes of Health. The United states Government has certain rights in the invention.
FIELD OF THE INVENTION
The present invention relates generally to the superfam~ly of nuclear receptors known as the steroid/thyroid hormone receptors and their cognate response elements. More particularly, the present invention relates to discovery of B-retinoic acid response elements (B~ARES), which may be used to enhance transcriptional activity of promoters.
BACKGROUND OF THE INVENTION.
A central question in eukaryotic molecular biology is how specific DNA-binding proteins bind regulatory sequences to influence cell function and fate. The steroid/thyroid hormone receptors form a superfamily of ligand-dependent transcription factors that are believed to play a part in such cell function and fate. For example, it is known that these receptors ~' transduce extracellular hormonal ~ignal to target genes that contain specific enhancer sequences referred to as hormone-response elements (HREs). Each receptor contains a ligand-binding domain and a DNA-binding domain. The receptor undergoes a conformational change when it binds ligand which conformational change permits the receptor-ligand complex to bind its cognate response element and thereby regulate transcriptional activity of an associated promoter, which drives transcription of an operatively associated structural gene.
Sequence comparison and mutational analyses of hormone receptors such as glucocorticoid receptor ~GR) have identified functional domains responsibl-e for 35 transcriptional activation and repression, nuclear ' ' localization, DNA binding, and hormone binding. The DNA
binding domain, which i5 required in order to activate .
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~vo 9l/n7~8x 2 0 7 2 ~ 4 ~ Pcr/~isgo/06626 transcription, consists of 66-68 amino acids of whlch about 20 sites, including nine cysteines (Cl to Cg), are invariant among different receptors. The modular structure of members of this receptor superfamily allows the exchange of one domain for another to create functional, chimeric receptors.
The hormone response elements are generally structurally related but in fact are functionally distinct. Those for GR (GRE), estrogen receptor (ERE), and thyroid hormone receptor response elements (TRE) have been characterized in detail; they consist of a palindromic pair of `half sites' (Evans, Science 240, 889 (1988); Green and Chambon, Trends In Genetics 4, 309 (1988)). With optimized pseudo- or consensus response elements, only two nucleotides per half site are different in GRE and ERE (Klock, et al., Nature 329, 734 (1987)). On the other hand, identical half sites can be seen in ERE and TRE, but their spacing is different (Glass, et al., Cell 54, 313 (1988)). Moreover, TRE has been shown to mediate transcriptional activation by transfected retinoic acid receptors (RARs) in CV-1 cells -whereas non-transfected cells show no response. (Umesono et al., Nature 336, 262 (1988)). In other words, both TR
and RR receptors can activate TREs.
It is, thus, surprising that the B-retinoic acid response elements (BRAREs) disclosed herein have a tandem repeat sequence as opposed to a palindromic sequence, and are much less susceptible to transcriptional activation by non-cognate receptors (e.g., estrogen receptor (ER), GR, thyroid hormone receptor (TR), etc.) than the known response elements (GRE, ERE, TRE~. Also surprising is ~that construct6 having BRAREs in a wide variety of mammalian cells have shown robust retinoic acid (RA)-dependent induction in the absence of cotransfected retinoic acid receptor (RAR)-encoding expression vector.

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: . ... ,.. : .. , wo gl/n7488 ` 2 0 7 2 ~ ~ ~ PCT/US90/06626 _3_ This discovery suggests that virtually all mammalian cells express a low level of endogenous BRAR that is sufficient for efficient activation of vectors containing the BRARE, but apparently below a threshold for activation of the previously studied TREs.
Thus, using transcriptional control reqions comprising BRARE and a functional promoter, it is now possible to provide recombinant DNA vectors containing a gene, the transcription (and, thereby, also expression) of which is under the control of a promoter, the transcriptional activity of which is responsive to (and increased by) retinoic acid, without the necessity of cotransfection with a vector providing expression o~
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SUMMARY OF THE INVENTION
We have discovered, and characterized by sequence, DNA segments which are BRAREs and linkages, between said segments and promoters, which are operative to confer responsiveness to retinoic acid on transcriptlonal activities of the promoters in mammalian cells. We have also discovered that the transeriptional activity enhancing effect of BRAREs occurs in all mammalian cells in the presence of retinoic acid, indicating that BRAR is present endogenously in all of these cells.
DETAILED DESCRIPTION OF THE INVENTION
In the present specification and claims, reference will be made to phrases and terms of art which are expressly defined for use herein as follows:
As used herein, RARB or B~AR means retinoic acid receptor beta.
As used herein, CAT means chloramphenicol acetyltransferease: LUC mean firefly luciferase; B-Gal means Bgalactosidase.
As used herein, COS means monkey kidney cells -U t L ~
~VO91/~74X~ ~ ~ PCT/~S90/06626 which express T antigen (Tag). See Gluzman, Cell, 23:175 (1~81).
As used herein, CV-l means mouse kidney cells from the cell line transferred to as "CV-l". CV-l is the parental line of COS. Unlike COS cells, which have been transformed to express SV40 T antigen (Tag), CV-l cells do not express T antigen.
As used herein, BRARE's mean B retinoic acid response elements. BRARE's are enhancer-like DNA
sequences that confer retinoic acid (RA) responsiveness via interaction with the BRAR-RA complex, to transcriptional activity of promoters linked operatively for such responsiveness to a BRARE.
As used herein, the terms "transcriptional control region" or "transcriptional control element", means a DNA segment comprising a BRARE operatively linked to a promoter to confer retinoic acid responsiveness to transcriptional activity of the promoter.
As used herein, in the phrase "operatively linked" means that the linkage (i.e., DNA ~egment) between the DNA segments so linked is such that the described effect of one of the linked segments on the other is capable of occuring.
Effecting operable linkages for the various purposes stated herein is well within the skill of those of ordinary skill in the art, particularly with the teaching of the instant specification.
As used herein, the phrase "promoter being naturally unresponsive to RA" means that that RA does not enhance transcription from the promoter to an observable extent in a mammalina cell unless a BRARE is spliced or inserted, by recombinant DNA or genetic engineering methods, into a DNA segment comprising the promoter upstream of thepromoter (relative to the direction of transcription therefrom) and linked to the promoter in a ; ~ ., , . - , :

\VO91/0~8~ 2 0 7 ~ ~ 4 ~ PCT/US90/06626 manner which makes operative responsiveness to RA of the transcriptional activity from the promoter.
Use of the term "substantial sequence homology"
in the present specification and claims means it is intended that DNA or RNA sequences which have de minimus sequence variations ~rom, and retain the same functions as, the actual sequences disclosed and claimed herein are within the scope of the appended claims.
The nucleotides which occur in the various nucleotide sequences appearing herein have their usual single-letter designations (A, G, T, C or U) used routinely in the art.
In the textual portion of the present specification and claims, references to Greek letters may be written as alpha, beta, etc. In the Figures and-elsewhere in the specification, the corresponding Greekletter symbols are sometimes used.
In one of its aspects, the invention is a vector for expression in a mammalian cell of a protein, said expression under control of a transcriptional control region of the vector, said transcriptional control region comprising (l) ~ promoter, which is linked operatively for transcription to a first DNA segment, which is expressed as the protein, and (2) a second DNA segment, which comprises a subsegment of sequence 5'-GTTCACnln2n3n4n5GTTCAC-3', wherein nl, -n2, n3, n4 and n5 are independently A, T, C or G, 6aid subsegment of said second DNA segment being linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that the transcriptional activity of the promoter is naturally unresponsive to retinoic acid.
With respect to the promoter which is part of a transcriptional control region of the invention, practically any promoter may be used., so long as the : ,. : : ,, - . - :

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\~'O91/07188 ~ 2 ~ ~2 6~ ~ r'CT/~590/~6626 transcriptional activity of such a promoter may be enhanced by a BRARE-containing DNA segment suitably positioned upstream from the promoter and provided that such promoter is naturally unresponsive, in its transcriptional activity, to retinoic acid. Among such promoters are Delta-MTV promoter, Herpes thymidine kinase ttk) promoter and basal SV-40 promoter. Very desirable are promoters which require a response element for activity. On the other hand, very strong promoters, which drive transcription in the absence of enhancers, are not desirAble promoters for use in the transcription control regions, and vectors, of the invention.
Virtually any protein or polypeptide of interest can be made with mammalian cell transformed with an expression vector of the invention. Such proteins include hormones, lymphokines, receptors or receptor subunits, immunoglobulin chains and the like. Indicator proteins such as LUC, CAT and ~-Gal can also be made.
In another of its aspects, the invention entails a mammalian cell transformed to express a protein from a vector for expression of said protein, said vector comprising a transcriptional control region comprising (l) a promoter, which is linked operatively for transcription to-a first DNA segment, which is expressed as the protein, and (2) a second DNA segment, which comprises a subsegment of sequence 5'-GTTCACnln2n3n4n5GTTCAC-3~, wherein nl, n2, n3, n4 and nS are independently A, T, C or G, said subsegment of said second DNA segment being linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that the transcriptional activity of the promoter is naturally unresponsive to retinoic acid.
Among the types of mammalian cells that can be transformed in accordance with the invention are CV-l, ' ' . ' ' ,: :

:' ' ' , , . ' ~vo 9l/n7~8~ ` ` 2 0 ~2 6 4 4 PCT/~S90/06626 COS, F9, Pl9, CH0, HeLa, NIH 3T3, Rat2 fibroblast, HT1080.T, chick embryo fibroblasts and quail QT6 cells.
In still ano.ther aspect, the invention entails method for testing activity of a test compound as an agonist or antagonist of retinoic acid, said meth~d comprising:
(a) culturing (i~ in the presence of retinoic acid and the absence of test compound and tii) in the presence of both retinoic acid and test compound, a mammalian cell transform to express a protein from a vector for expression of said protein, said vector comprising a transcriptional control region comprising (1) a promoter, which is linked operatively for transcription to a fixst DNA segment, which is expressed as the protein, and (2) a second DNA segment, which comprises a subsegment of sequence 5'-GTTCACn1n2n3n4n5GTTCAC-3', wherein n1, n2, n3, n4 and n5 are independently A, T, C or G, said subsegment of said second DNA segment being linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that the transcriptional activity of the promoter is naturally unresponsive to retinoic acid;
and (b) comparing the amount of said protein expressed during the two culturing of step (a~.
The cells of the invention, including those employed in the method of testing compounds for RA
activity, can optionally be co-transformed with an expression vector which expresses BRAR.
Indeed, because a low level of responsiveness of BRAREs (in enhancing transcription from an operatively linked promoter) has also been observed with TR's and vitamin D3 receptor (YD3R), agonists and antagonists of ~ :
thyroid hormones and vitamin D3 can be screened for by '., . , ',, ~ . : .,.......... , . :
.: , , ., , ' : . ' . : : ' ', ' .: ~
.: , - . . , . . . . .. . ~:

~'O 91/074X8 2 0 7 2 6 ~ ~ PC~r/~'S90/06626 testing compounds, as described above, but using cells transfected with a suitable vector of the present invention an~ a vector expressing TR or VD3R.
Receptors, assay methods, and other subject matter pertinent to the subject matter of the present specification may be found in the following references, which are incorporated herein by reference: Commonly assigned United States Patent Application Serial No. 108,47~, filed October 20, 1987 and published as PCT
10 International Publication No. WO 88/03168; commonly assigned IJnited States Patent Application Serial No. 276,536, filed November 30, 1988 and published as European Patent Application Publication No. 0 325 849;
commonly assigned United States Patent Application Serial 15 No. 370,~0~, filed June 22, 1989, said Application listing a Budapest Treaty Deposit of a plasmid harboring a cDNA encoding a gamma-retinoic acid receptor, said deposit having been made June 22, 1989 and bearing American Type Culture Collection Accession No. 40623;
20 Zelent et a.l., Nature ~, 714 ~1989); Petkovich et al., Nature 330, ~44 (1987); Brand et al., Nature 332, 850 (19~8).
In another of its aspects, the present invention entails a D~A segment for controlling transcription of a gene in a mammalian cell, said se~ment comprising a pr~moter linked operatively for transcription to the gene and a 6ubscsment with the sequence 5'-GTTCACnln~n3n4n5GTTC~C-3', wherein nl, n2, n3, n4 and n5 are independently A, T, G or C, said subsegment linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that transcriptional activity fr~m the promoter is naturally unresponsive to retinoic acid.

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\Vo 9l /n7~x 2 0 7 2 ~ ~ 4 PC r/~IS90/06626 ~'~ g BRARE may be provided on a DNA segment which possesses a tandem repeat of the 6 bp motif 5'-GTTCAC
separated by 5 bp sequence, which sequence may be any randomly chosen nucleotide sequence. Especially preferred BRAREs are provided on the segments 5'-AAGCTTAAGGGTTCACCGAAAGTTCACTCAGCTT, 5'-AAGCTTAAGGGTTCACCGAAAGTTCACTCGCATAGCTT and 5'-AAGCTTAAGGGTTCACCGAAAGTTCACTCGCATATATTAGCTT, which DNA
segments are adapted at the 5'- and 3'- ends to incIude a convenient restriction endonuclease site.
Because the DNA segments which comprise the BRARE are relatively short, they may be provided synthetically, that is by synthesizing the BRARE-containing oligonucleotide on a DNA synthesizer as is known in the art. It is very desirable to provide restriction endonuclease sites at the 3' and 5' end of the oligomer, such that the synthetic BRARE may be conveniently inserted into a DNA expression vector at a site upstream from the promoter, whose transcriptional ao~ivity is to be enhanced and which driving transcription of the desired gene. As those of ordinary skill in the art will understand, BRAREs, like other response elements, and orientation and, with wide latitude, position independent. Thus, BBRARE is functional in either orientation and may be placed in any convenient location from about 30 nucleotides upstream to about 10,000 nucleotides upstream from the promoter to be affected.
Preferred mammalian cells for use with the enhanced expression systems of the invention employing transcriptional control regions comprising beta-retinoic acid response element are COS cells and ~V-l cells.
COS-l (referred to as COS) cells are mouse kidney cells that express SV40 T antigen (Tag); CV-1 do not express SV40 Tag. CV-l cells are convenient because they lack : ' ~ ' ,: ' : . . ..................... ': '.: . :: . . : , : . . . , , ...: . . :
. .

~o sl/n7~s ~ PCT/l.iS90/06626 ,' --lo-- ~;! t any endogenous glucocorticoid or mineralocorticoid or other known steroid or thyroid hormone receptors, except that they do produce low levels of BR~R. Thus, via gene transfer with appropriate expression vectors comprising a heterologous gene under the control of a transcriptional control region of the invention, it is possible to convert these host cells into transformed cells which produce increased quantities of a desired protein in response to induction by retinoic acid.
Expression plasmids containing the SV40 origin of replication, can propagate to high copy number in any host cell which expresses SV40 Tag. Thus, expression plasmids carrying the SV40 origin of replication can replicate in COS celis, but not in CV-1 cells. Although increased expression afforded by high copy number is desirable, it is not critical to the disclosed assay system. The use of any particular cell line as a host is also not critical, although CV-l cells are preferred because they are particularly convenient for gene transfer studies and provide a sensitive and well described host cell system.

EXAMPLE
The following demonstrates that the sequences in the promoter of the mouse RARb gene confer RA
responsiveness, and that these sequences represent a target specific for the three RA receptor subclasses (alpha-, beta- and gamma-RAR). The RA response element ~RARE) does not mediate significant transcriptional activation by estrogen, glucocorticoidj but does weakly (about one order of magnitude less) mediate transcriptional activatin by vitamin D or thyroid hormone receptors (complexed with cognate ligands).
A mouse liver genomic DNA library (Clonetech~ in lambda vector EMBL3 was scxeened with a human RARb sDNA

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~vo 9l~n7~ 2 0 7 2 6 4 4 PCT/US90/06626 probe to localize the RARE in the RARb gene. This resulted in the isolation of a genomic fragment containing approximately 10 kb of upstream sequence, the complete first exon, and 10 kb of the first intron. The sequence of a portion of this clone containing the first exon and proximal 5' DNA is shown in Figure 1. The 10 kh upstream region was fused in-frame just downstream of the RARb translation initiation codon to a b-galactosidase reporter gene ~Fig. 2a). RAR-PL-bGAL was introduced int~
monkey kidney CV-1 cells cotransfected with RAR
expression vector. Enzyme activity was induced upon retinoic acid addition, indicating that this region of genomic DNA contains a functional promoter which is responsive to retinoic acid. This was accomplished by introducing a SalI restriction site was introduced into the genomic clone at the indicated position by site-directed mutagenesis; the 10 kb genomic fragment was then excised and cloned into the b-galactosidase vector pLSV (a derivative of pGH101 (Herman, G.E., 0'9rien, W.E.
and Beaudet, A.L. Nucl. Acids Res., 14, 7130 (1986), modified to contain a SalI site and a polylinker sequence by oligo addition, to yield RAR-PL-bGAL.
A series of deletions from the 5' end of RAR-PL-bGAL reveal that sequences mediating RA induction reside within the 2 kb NheI-SacII fragment (Fig. 2a;
Table below). Subfragments of this region were cloned into the enhancer-dependent luciferase reporter plasmid DMTV-LUC, which contains the mouse mammary tumor virus promoter with the natural GR response elements deleted ~Hollenberg, S.M. and Evans, R.M. Cell, 55, 899-906 (1988)). A 183 bp SmaI fragment (see Fig. 1) is able to confer retinoic acid responsiveness to this heterologous promoter in either orientation (Table). Oligonucleotide sequences (Fig. 2b) derived from this region were then used to further define the RA response element, either in - ;- - .... . .
.. . .; . . . . , , . ~ . ~:

, ,- ., :. -~O91/07~X~ PCT/US90/06626 2~726~ll DMTV-LUC or DMTV-CAT (Table below).
Thyroid hormone response element (TRE) has been shown to mediate transcriptional activation by transfected RARs in CV-l cells, whereas non-transfected cells show no response. Umesono et al, Nature 336, 262-265 ~1988). Surprisingly, when Delta-MTV-CAT
constructs ~REl, BRE2, and BRE3 (Figur~ 2) showed robust RA-dependent induction in the absence of cotransfected RAR expression vector. Cotransfection of RAR-alpha expression vector increased induction by only two-fold, which demonstrates that CV-l cells express a low level of endogenous RA receptor that is sufficient for efficient activation of vectors containing the BRE, but apparently below a threshold for~activation of the previously studied TREs. A survey of the following cell lines indicated that all were able to efficiently transactivate the BRARE in an RA-dependent fashion in the absence of transfected RAR expression vector: CV-l, F9 and Pl9 (mouse teratocarcinomas), CH0, HeLa, NIH 3T3, Rat2 fibroblasts, HT1080.T (human lymphoid), chick embryo fibroblasts, and quail QT6 cells. No cell line has yet been tested which does not express this activity.
vector.
Inspection of the sequences of BREl, BRE2 and BRE3 (Fig. 2b) identifies a tandem repeat of the 6 bp motif GTTCAC. The center to center separation of 11 bp between these repeats is one turn of the DNA helix.
Constructs containing single copies of either the 5' or 3' half site (BRE4 and BRE5) are functional only upon cotransfection of RAR expression vectors (Figure 2d).
Not only does this indicate that the RARE is a honafide target of all three RAR subtypes expressed from cloned cDNA, but also demonstrates that these half sites can serve as a minimal RA response element in the context of the Delta-MTV promoter. Apparently a single half-site , wo 9l~n7~88 2 0 7 2 6 4 ~ PCT/US90/06626 (5'-GTTCAC-3~) is a low affinity target requiring high levels of receptor for activation, and that the two sequences, when ~uxtaposed as a tandem repeat, create a high affinity binding site (via cooperative interactions) which is able to respond to the low level of endogenous RAR present in CV-l and other cells.
To demonstrate that the sequences described above are direct binding ~ites for the RAR, extracts from transfected cells were mixed with 32P-labeled RARE, and the resulting complex immunoprecipitated with antibody specific to the transfected receptor. For this purpose, a hybrid receptor (termed GRR) was created ln which the amino terminus of the glucocorticoid receptor was coupled to the DNA binding and ligand binding domains of RARa.
This hybrid receptor exhibits the RA dependence and target gene specificity of the RAR. (D. Mangelsdorf et al. unpublished observations). COS cell extracts containing the hybrid receptor specifically immunoprecipitate labeled BRE2 oligo. Binding of GRR to BRE2 i~ this assay is not affectea by the addition of an excess of unlabeled GRE competitor, but is competed by an excess of either the B-response element itself or a TRE
sequence, another known RAR binding site. In a parallel set of experiments, GR extract specifically binds to labeled GRE, i~ competed by excess unlabeled GRE, and does not recognize the BRE2 sequence. Thus, specific -binding to the B-response element is observed by the hybrid GRR receptor.
Many previously characterized response elements are targets of more than one type of receptor: both the RAR and the TR are able to activate a TRE: the RAR, TR, and estrogen receptor all activate the vitellogenin ERE;
the progesterone, mineralocorticoid, and GR all activate the GRE (Ham et al., Nucl. Acids Res. 16, 5263-5276 (1988)). Thus, it might be expected that the response . . .

. .

\~091/074X~ 2 ~ 7 2 6 ~ ~ ICT/~S90/06626 element of the ~ARb gene would reciprocally be responsive to the TR, ER, and/or other members of the receptor superfamily. Cotransfection of the ER, GR, in CV-1 cells with construct BREl failed to result in appreciable activation in the absence or following addition of the appropriate ligand, although cotransfecti~n with TR and vitamin D receptor (VD3R) CV-l cells with construct BRE1 did weakly (about 10- to 20-fold less) activate their cognate response elements.
lo 5 ug of each of the constructs indicated in the Table below were transfected into CV-1 cells with either RSV LUC or RSV-bGAL to normalize transfection efficiencies. Transfections also included RARa expression vector. Each value represents duplicate measurements of plates treated with 10 7M RA (~GAL
experiments) or 10 6M RA (luciferase experiments) relative to plates treated with solvent only. The 183 bp SmaI restriction fragment (shown in Figure 1) was inserted either in the forward (F) or reverse (R) orientation relative to the Delta-~TV promoter. The (NR) construct contains a 45 bp oligo sequence located 24 bp 3' of bREl in the RARb promoter which was nonresponsive to RA.
Plasmids were transfected into CV-1 cells and assayed for B-galactosidase activity eit~er without or with the addition of 10 7M RA. Negative responses were two-fold induction or less: positive inductions were 6even-fold or greater.
Cells were transfected in 10 cm dishes with 10 ug DNA containing 5 ug reporter plasmid, 1-2 ug either RSV-LUC (a), or RSV-bGAL or pCHllO (c and d), pGEM4 as carrier DNA, and for the experiments shown in a and d, 1 ug RSV-RAR expression vector or the same amount of an RSV
vector genPrating a nonsense transcript. Cells were harvested 1 day after addition of retinoic acid. All CAT

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~VO91/07~8 '2 0 7 2 6 4 ~ PCT/US90/06626 assays represent equivalent amounts of b-galactosidase activity; bGAL assays were normali~ed to luciferase activity.

Retinoic acid inducibilitv of reporter constructs Construct Fold increase RAR-PL-bGAL 14 10 RAR-DXN-bGAL 22 RAR-DNhSc-bGAL 2 DMTV-Smal83F-LUC lO
DMTV-Smal83R-LUC 9 DMTV-(NR)-LUC 2 DMTV-bREl-LUC 14 DESCRIPTION OF THE DRAWINGS
Figure l represents the sequence of the mouse ~RAR promoter region and first exon. The TATA and GTTCAC
motifs are underlined; the first exon splice site is indicated with an arrow. A mouse liver genomic DNA
library (Clonetech) in the lambda vector EMBL3 was screened with the BamHI-SphI fragment of the human RARb cDNA clone Bl-RARe. See, Benbrook et al, Nature 333, 669-672 (1988). This probe contains only first exon sequences, which are unique to the ~AR gene. A clone harboring a 20 kb insert was isolated, and the region surrounding the first exon subcloned and subjected to dideoxy sequence analysis.
Figure 2(a) represents the in vivo analysis of RARB RA response element sequences, following a series of deletions from the 5' end of the sequence including the B
retinoic acid response element. The sequence at the junction between the mouse RAR~ gene and the ~ .
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.~, ... , . . . , : . - . . . .:, . . :.. : .: .: .. . ... . .

.~ . : .. , . ,. . . . ... ., ... ... . , . ~ :::, .... . . .. . .

. . .. . .. .. . .. .. . . . . . . . . .. .. . ... .. . ... . -~VO91/07~88 2 ~ ~ 2 6' ~ ~ PCT/US90/06626 B-galactosidase reporter gene is as shown. Numbered amino acids correspond to the native RARB translation product. Restriction sites are N, NotI; X, XhoI; K, KpnI; S, SalI; Nh, NneI; Sc, SacII. The dotted line represents plasmid sequences.
Figure 2(b) represents sequences of oligonucleotides including the B retinoic acid response element used in these experiments. The terminal lower case bases are foreign to the RARB promoter, and were included to allow insertion into the unique HindIII site of the Delta-MTV vector.

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Claims (16)

We Claim:

1. A vector for expression in a mammalian cell of a protein, said expression under control of a transcriptional control region of the vector, said transcriptional control region comprising (1) a promoter, which is linked operatively for transcription to a first DNA segment, which is expressed as the protein, and (2) a second DNA segment, which comprises a subsegment of sequence , wherein n1, n2, n3, n4 and n5 are independently A, T, C
or G, said subsegment of said second DNA segment being linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that the transcriptional activity of the promoter is naturally unresponsive to retinoic acid.

2. A vector according to Claim 1 wherein n is C, n2 is G, n3 is A, n4 is A and n5 is A.

3. A vector according to Claim 2 wherein said subsegment of said second DNA segment is a subsegment of the segment of sequence .

4. A vector according to Claim 3 wherein said segment, , of said second DNA segment is a subsegment of the segment of sequence .

5. A vector according to Claim 4 wherein said segment, , of said second DNA segment is a subsegment of the segment of sequence .

6. A recombinant DNA vector according to any of Claims 1-5 wherein wherein said promoter is the delta-MTV
promoter of mouse mammary tumor virus.

7. A vector according to Claim 6 wherein the protein expressed under control of said transcriptional control region is selected from the group consisting of luciferase, chloramphenicol acetyltransferase and beta-galactosidase.

8. A mammalian cell transformed to express a protein from a vector for expression of said protein, said vector comprising a transcriptional control region comprising (1) a promoter, which is linked operatively for transcription to a first DNA segment, which is expressed as the protein, and (2) a second DNA segment, which comprises a subsegment of sequence , wherein n1, n2, n3, n4 and n5 are independently A, T, C or G, said subsegment of said second DNA segment being linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that the transcriptional activity of the promoter is naturally unresponsive to retinoic acid.

9. A mammalian cell according to Claim 8, wherein the cell is of a type selected from the group consisting of CV-1, COS, F9, P19, CHO, HeLa, NIH 3T3, Rat2 fibroblasts, HT1080.T, chick embryo fibroblast and quail QT6 cells.

10. A method for testing activity of a test compound as an agonist or antagonist of retinoic acid, said method comprising:
(a) culturing (i) in the presence of retinoic acid and the absence of test compound and (ii) in the presence of both retinoic acid and test compound, a mammalian cell transform to express a protein from a vector for expression of said protein, said vector comprising a transcriptional control region comprising (1) a promoter, which is linked operatively for transcription to a first DNA segment, which is expressed as the protein, and (2) a second DNA segment, which comprises a subsegment of sequence 5'-GTTCACn1n2n3n4n5GTTCAC-3', wherein n1, n2, n3, n4 and n5 are independently A, T, C or G, said subsegment of said second DNA segment being linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that the transcriptional activity of the promoter is naturally unresponsive to retinoic acid;
and (b) comparing the amount of said protein expressed during the two culturing of step (a).

11. A DNA segment for controlling transcription of a gene in a mammalian cell, said segment comprising a promoter linked operatively for transcription to the gene and a subsegment with the sequence 5'-GTTCACn1n2n3n4n5GTTCAC-3', wherein n1, n2, n3, n4 and n5 are independently A, T, G or C, said subsegment linked operatively to said promoter to confer responsiveness to retinoic acid on transcriptional activity from the promoter, provided that transcriptional activity from the promoter is naturally unresponsive to retinoic acid.

12. A DNA segment according to Claim 11 wherein n1 is C, n2 is G, n3 is A, n4 is A and n5 is A.

13. A DNA segment according to Claim 12 wherein said subsegment of sequence is a subsegment of the segment of sequence .

14. A DNA segment according to Claim 14 wherein said segment of sequence is a subsegment of the segment of sequence .

15. A DNA segment according to Claim 14 wherein said segment of sequence is a subsegment of the segment of sequence .

16. A DNA segment according to any of Claims 11-15 wherein the promoter is the delta-MTV promoter of mouse mammary tumor virus.