Two novel RXR alpha isoforms from mouse testis

被引:30
作者
Brocard, J [1 ]
Kastner, P [1 ]
Chambon, P [1 ]
机构
[1] ULP,COLL FRANCE,INSERM,CNRS,INST GENET & BIOL MOL & CELLULAIRE,F-67404 ILLKIRCH GRAFFENS,FRANCE
关键词
D O I
10.1006/bbrc.1996.1782
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the isolation from mouse testis cDNA of two novel RXR alpha isoforms, mRXR alpha 2 and mRXR alpha 3, with distinct sequences upstream of exon 2. These two isoforms encode a similar protein (mRXR alpha 2/3) which lacks the 28 N-terminal amino acid residues of the major RXR alpha isoform, mRXR alpha 1. The N-terminal activation function (AF-1) of mRXR alpha 2/3 appears altered when compared to that of mRXR alpha 1. mRXR alpha 2 and mRXR alpha 3 are specifically expressed in the testis, and their expression is strongly upregulated in this tissue at puberty. These observations increase the molecular complexity of RXRs, and indicate that RXR alpha may play a specific function during spermatogenesis. (C) 1996 Academic Press, Inc.
引用
收藏
页码:211 / 218
页数:8
相关论文
共 35 条
  • [11] 2 DISTINCT ESTROGEN-REGULATED PROMOTERS GENERATE TRANSCRIPTS ENCODING THE 2 FUNCTIONALLY DIFFERENT HUMAN PROGESTERONE-RECEPTOR FORM-A AND FORM-B
    KASTNER, P
    KRUST, A
    TURCOTTE, B
    STROPP, U
    TORA, L
    GRONEMEYER, H
    CHAMBON, P
    [J]. EMBO JOURNAL, 1990, 9 (05) : 1603 - 1614
  • [12] Kastner P., 1994, Vitamin A in health and disease., P189
  • [13] GENETIC-ANALYSIS OF RXR-ALPHA, DEVELOPMENTAL FUNCTION - CONVERGENCE OF RXR AND RAR SIGNALING PATHWAYS IN HEART AND EYE MORPHOGENESIS
    KASTNER, P
    GRONDONA, JM
    MARK, M
    GANSMULLER, A
    LEMEUR, M
    DECIMO, D
    VONESCH, JL
    DOLLE, P
    CHAMBON, P
    [J]. CELL, 1994, 78 (06) : 987 - 1003
  • [14] THE DROSOPHILA ECR GENE ENCODES AN ECDYSONE RECEPTOR, A NEW MEMBER OF THE STEROID-RECEPTOR SUPERFAMILY
    KOELLE, MR
    TALBOT, WS
    SEGRAVES, WA
    BENDER, MT
    CHERBAS, P
    HOGNESS, DS
    [J]. CELL, 1991, 67 (01) : 59 - 77
  • [15] MULTIPLICITY GENERATES DIVERSITY IN THE RETINOIC ACID SIGNALING PATHWAYS
    LEID, M
    KASTNER, P
    CHAMBON, P
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (10) : 427 - 433
  • [16] PURIFICATION, CLONING, AND RXR IDENTITY OF THE HELA-CELL FACTOR WITH WHICH RAR OR TR HETERODIMERIZES TO BIND TARGET SEQUENCES EFFICIENTLY
    LEID, M
    KASTNER, P
    LYONS, R
    NAKSHATRI, H
    SAUNDERS, M
    ZACHAREWSKI, T
    CHEN, JY
    STAUB, A
    GARNIER, JM
    MADER, S
    CHAMBON, P
    [J]. CELL, 1992, 68 (02) : 377 - 395
  • [17] LEID M, 1992, CELL, V71, P886
  • [18] THE MOUSE RETINOID-X RECEPTOR-GAMMA GENE - GENOMIC ORGANIZATION AND EVIDENCE FOR FUNCTIONAL ISOFORMS
    LIU, Q
    LINNEY, E
    [J]. MOLECULAR ENDOCRINOLOGY, 1993, 7 (05) : 651 - 658
  • [19] POLYMERASE CHAIN-REACTION WITH SINGLE-SIDED SPECIFICITY - ANALYSIS OF T-CELL RECEPTOR DELTA-CHAIN
    LOH, EY
    ELLIOTT, JF
    CWIRLA, S
    LANIER, LL
    DAVIS, MM
    [J]. SCIENCE, 1989, 243 (4888) : 217 - 220
  • [20] HIGH POSTNATAL LETHALITY AND TESTIS DEGENERATION IN RETINOIC ACID RECEPTOR-ALPHA MUTANT MICE
    LUFKIN, T
    LOHNES, D
    MARK, M
    DIERICH, A
    GORRY, P
    GAUB, MP
    LEMEUR, M
    CHAMBON, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (15) : 7225 - 7229