FACT relieves DSIF/NELF-mediated inhibition of transcriptional elongation and reveals functional differences between P-TEFb and TFIIH

被引:92
作者
Wada, T
Orphanides, G
Hasegawa, J
Kim, DK
Shima, D
Yamaguchi, Y
Fukuda, A
Hisatake, K
Oh, S
Reinberg, D
Handa, H
机构
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Tokyo Inst Technol, Frontier Collaborat Res Ctr, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[3] Saitama Med Sch, Dept Biochem, Iruma, Saitama 3500451, Japan
[4] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Biochem, Howard Hughes Med Inst,Div Nucl Acids Enzymol, Piscataway, NJ 08854 USA
关键词
D O I
10.1016/S1097-2765(00)80272-5
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 that the chromatin-specific transcription elongation factor FACT functions in conjunction with the RNA polymerase II CTD kinase P-TEFb to alleviate transcription inhibition by DSIF (DRB sensitivity-inducing factor) and NELF (negative elongation factor). We find that the kinase activity of TFIIH is dispensable for this activity, demonstrating that TFIIH-mediated CTD phosphorylation is not involved in the regulation of FACT and DSIF/NELF activities. Thus, we propose a novel transcriptional regulatory network in which DSIF/NELF inhibition of transcription is prevented by P-TEFb in cooperation with FACT. This study uncovers a novel role for FACT in the regulation of transcription on naked DNA that is independent of its activities on chromatin templates. In addition, this study reveals functional differences between P-TEFb and TFIIH in the regulation of transcription.
引用
收藏
页码:1067 / 1072
页数:6
相关论文
共 24 条
  • [1] mRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domain
    Cho, EJ
    Takagi, T
    Moore, CR
    Buratowski, S
    [J]. GENES & DEVELOPMENT, 1997, 11 (24) : 3319 - 3326
  • [2] Reversible phosphorylation of the C-terminal domain of RNA polymerase II
    Dahmus, ME
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (32) : 19009 - 19012
  • [3] Evidence that Spt4, Spt5, and Spt6, control transcription elongation by RNA polymerase II in Saccharomyces cerevisiae
    Hartzog, GA
    Wada, T
    Handa, H
    Winston, F
    [J]. GENES & DEVELOPMENT, 1998, 12 (03) : 357 - 369
  • [4] Hartzog GA, 1996, MOL CELL BIOL, V16, P2848
  • [5] Eukaryotic transcription: An interlaced network of transcription factors and chromatin-modifying machines
    Kadonaga, JT
    [J]. CELL, 1998, 92 (03) : 307 - 313
  • [6] Kimmelman J, 1999, MOL CELL BIOL, V19, P4774
  • [7] Immunoaffinity purification of the human multisubunit transcription factor IIH
    LeRoy, G
    Drapkin, R
    Weis, L
    Reinberg, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (12) : 7134 - 7140
  • [8] Maldonado E, 1996, METHOD ENZYMOL, V274, P72
  • [9] CONTROL OF FORMATION OF 2 DISTINCT CLASSES OF RNA POLYMERASE-II ELONGATION COMPLEXES
    MARSHALL, NF
    PRICE, DH
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) : 2078 - 2090
  • [10] Control of RNA polymerase II elongation potential by a novel carboxyl-terminal domain kinase
    Marshall, NF
    Peng, JM
    Xie, Z
    Price, DH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (43) : 27176 - 27183