A TRANSFERABLE SILENCING DOMAIN IS PRESENT IN THE THYROID-HORMONE RECEPTOR, IN THE V-ERBA ONCOGENE PRODUCT AND IN THE RETINOIC ACID RECEPTOR

被引:268
作者
BANIAHMAD, A [1 ]
KOHNE, AC [1 ]
RENKAWITZ, R [1 ]
机构
[1] MAX PLANCK INST BIOCHEM,W-8033 MARTINSRIED,GERMANY
关键词
RETINOIC ACID RECEPTOR; SILENCER; THYROID HORMONE RECEPTOR; V-ERBA;
D O I
10.1002/j.1460-2075.1992.tb05140.x
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
Inhibition of gene transcription is brought about by several mechanisms. The least understood mechanism is probably silencing, the analogue to transcriptional enhancing. We provide evidence that the silencing function of the oncogene product v-ERBA or the cellular counterpart, the thyroid hormone receptor (TR, c-erbA) is located in the C-terminal part and is transferable to a heterologous DNA binding domain. Deletion analyses suggest an important role for a basic and hydrophilic amino acid stretch on both ends of the domain. In addition we show that the related retinoic acid receptor (RAR) also contains a functional silencing domain similar in size and amino acid sequence. However, the activity of this domain can be neutralized by an additional domain in the C-terminus which functions cell specifically.
引用
收藏
页码:1015 / 1023
页数:9
相关论文
共 49 条
  • [1] ACTIVITY OF 2 DIFFERENT SILENCER ELEMENTS OF THE CHICKEN LYSOZYME GENE CAN BE COMPENSATED BY ENHANCER ELEMENTS
    BANIAHMAD, A
    MULLER, M
    STEINER, C
    RENKAWITZ, R
    [J]. EMBO JOURNAL, 1987, 6 (08) : 2297 - 2303
  • [2] MODULAR STRUCTURE OF A CHICKEN LYSOZYME SILENCER - INVOLVEMENT OF AN UNUSUAL THYROID-HORMONE RECEPTOR-BINDING SITE
    BANIAHMAD, A
    STEINER, C
    KOHNE, AC
    RENKAWITZ, R
    [J]. CELL, 1990, 61 (03) : 505 - 514
  • [3] BANIAHMAD C, 1991, IN PRESS J MOL BIOL
  • [4] C-ERBA ENCODES MULTIPLE PROTEINS IN CHICKEN ERYTHROID-CELLS
    BIGLER, J
    EISENMAN, RN
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (10) : 4155 - 4161
  • [5] BRENT G A, 1989, New Biologist, V1, P329
  • [6] A MECHANISM FOR SYNERGISTIC ACTIVATION OF A MAMMALIAN GENE BY GAL4 DERIVATIVES
    CAREY, M
    LIN, YS
    GREEN, MR
    PTASHNE, M
    [J]. NATURE, 1990, 345 (6273) : 361 - 364
  • [7] AN AMINO-TERMINAL FRAGMENT OF GAL4 BINDS DNA AS A DIMER
    CAREY, M
    KAKIDANI, H
    LEATHERWOOD, J
    MOSTASHARI, F
    PTASHNE, M
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1989, 209 (03) : 423 - 432
  • [8] DEVELOPMENTAL REGULATION OF BETA-GLOBIN GENE SWITCHING
    CHOI, ORB
    ENGEL, JD
    [J]. CELL, 1988, 55 (01) : 17 - 26
  • [9] A SINGLE POINT MUTATION IN ERBA RESTORES THE ERYTHROID TRANSFORMING POTENTIAL OF A MUTANT AVIAN ERYTHROBLASTOSIS VIRUS (AEV) DEFECTIVE IN BOTH ERBA AND ERBB ONCOGENES
    DAMM, K
    BEUG, H
    GRAF, T
    VENNSTROM, B
    [J]. EMBO JOURNAL, 1987, 6 (02) : 375 - 382
  • [10] PROTEIN ENCODED BY V-ERBA FUNCTIONS AS A THYROID-HORMONE RECEPTOR ANTAGONIST
    DAMM, K
    THOMPSON, CC
    EVANS, RM
    [J]. NATURE, 1989, 339 (6226) : 593 - 597