Human TATA-binding protein-related factor-2 (hTRF2) stably associates with hTFIIA in HeLa cells

被引:103
作者
Teichmann, M
Wang, ZX
Martinez, E
Tjernberg, A
Zhang, D
Vollmer, F
Chait, BT
Roeder, RG
机构
[1] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Labs Mass Spectrometry & Gaseous Ion Chem, New York, NY 10021 USA
关键词
D O I
10.1073/pnas.96.24.13720
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The TATA-binding protein (TBP)-related factor TRF1, has been described in Drosophila and a related protein, TRF2, has been found in a variety of higher eukaryotes. We report that human (h)TRF2 is encoded by two mRNAs with common protein coding but distinct 5' nontranslated regions. One mRNA is expressed ubiquitously (hTRF2-mRNA1), whereas the other (hTRF2-mRNA2) shows a restricted expression pattern and is extremely abundant in testis. In addition, we show that hTRF2 forms a stable stoichiometric complex with hTFIIA, but not with TAFs, in HeLa cells stably transfected with flag-tagged hTRF2. Neither recombinant human (rh)TRF2 nor the native flag.hTRF2-TFIIA complex is able to replace TBP or TFIID in basal or activated transcription from various RNA polymerase II promoters. Instead, rhTRF2, but not the flag.hTRF2-TFIIA complex, moderately inhibits basal or activated transcription in the presence of rhTBP or flag TFIID. This effect is either completely (TBP-mediated transcription) or partially (TFIID-mediated transcription) counteracted by addition of free TFIIA. Neither rhTRF2 nor flag.hTRF2-TFIIA has any effect on the repression of TFIID-mediated transcription by negative cofactor-2 (NC2) and neither substitutes for TBP in RNA polymerase III-mediated transcription.
引用
收藏
页码:13720 / 13725
页数:6
相关论文
共 39 条
  • [1] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [2] Assembly of the isomerized TFIIA-TFIID-TATA ternary complex is necessary and sufficient for gene activation
    Chi, TH
    Carey, M
    [J]. GENES & DEVELOPMENT, 1996, 10 (20) : 2540 - 2550
  • [3] A NEW FACTOR RELATED TO TATA-BINDING PROTEIN HAS HIGHLY RESTRICTED EXPRESSION PATTERNS IN DROSOPHILA
    CROWLEY, TE
    HOEY, T
    LIU, JK
    JAN, YN
    JAN, LY
    TJIAN, R
    [J]. NATURE, 1993, 361 (6412) : 557 - 561
  • [4] ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI
    DIGNAM, JD
    LEBOVITZ, RM
    ROEDER, RG
    [J]. NUCLEIC ACIDS RESEARCH, 1983, 11 (05) : 1475 - 1489
  • [5] Protein identification using mass spectrometric information
    Fenyö, D
    Qin, J
    Chait, BT
    [J]. ELECTROPHORESIS, 1998, 19 (06) : 998 - 1005
  • [6] Ge H, 1996, METHOD ENZYMOL, V274, P57
  • [7] Transcription properties of a cell type-specific TATA-binding protein, TRF
    Hansen, SK
    Takada, S
    Jacobson, RH
    Lis, JT
    Tjian, R
    [J]. CELL, 1997, 91 (01) : 71 - 83
  • [8] PURIFICATION OF HIS-TAGGED PROTEINS IN NONDENATURING CONDITIONS SUGGESTS A CONVENIENT METHOD FOR PROTEIN-INTERACTION STUDIES
    HOFFMANN, A
    ROEDER, RG
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (22) : 6337 - 6338
  • [9] TATA-BINDING PROTEIN RESIDUES IMPLICATED IN A FUNCTIONAL INTERPLAY BETWEEN NEGATIVE COFACTOR NC2 (DR1) AND GENERAL FACTORS TFIIA AND TFIIB
    KIM, TK
    ZHAO, YM
    GE, H
    BERNSTEIN, R
    ROEDER, RG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (18) : 10976 - 10981
  • [10] KOBAYASHI N, 1995, MOL CELL BIOL, V15, P6465