Different phosphorylated forms of RNA polymerase II and associated mRNA processing factors during transcription

被引:841
作者
Komarnitsky, P [1 ]
Cho, EJ [1 ]
Buratowski, S [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
关键词
RNA polymerase II; TFIIH; capping enzyme; Kin; 28;
D O I
10.1101/gad.824700
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The activities of several mRNA processing factors are coupled to transcription through binding to RNA polymerase II (Pol II). The largest subunit of Pol LI contains a repetitive carboxy-terminal domain (CTD) that becomes highly phosphorylated during transcription. mRNA-capping enzyme binds only to phosphorylated CTD, whereas other processing factors may bind to both phosphorylated and unphosphorylated forms. Capping occurs soon after transcription initiation and before other processing events, raising the question of whether capping components remain associated with the transcription complex after they have modified the 5' end of the mRNA. Chromatin immunoprecipitation in Saccharomyces cerevisiae shows that capping enzyme cross-links to promoters but not coding regions. In contrast, the mRNA cap methyltransferase and the Hrp1/CFIB polyadenylation factor cross-link to both promoter and coding regions. Remarkably, the phosphorylation pattern of the CTD changes during transcription. Ser 5 phosphorylation is detected primarily at promoter regions dependent on TEIIH. In contrast, Ser 2 phosphorylation is seen only in coding regions. These results suggest a dynamic association of mRNA processing factors with differently modified forms of the polymerase throughout the transcription cycle.
引用
收藏
页码:2452 / 2460
页数:9
相关论文
共 38 条
  • [1] TRANSCRIPTION-DEPENDENT REDISTRIBUTION OF THE LARGE SUBUNIT OF RNA-POLYMERASE-II TO DISCRETE NUCLEAR DOMAINS
    BREGMAN, DB
    DU, L
    VANDERZEE, S
    WARREN, SL
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 129 (02) : 287 - 298
  • [2] CADENA DL, 1987, J BIOL CHEM, V262, P12468
  • [3] A specific RNA-protein interaction at yeast polyadenylation efficiency elements
    Chen, SX
    Hyman, LE
    [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (21) : 4965 - 4974
  • [4] 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
  • [5] THE ROLE OF MULTISITE PHOSPHORYLATION IN THE REGULATION OF RNA-POLYMERASE-II ACTIVITY
    DAHMUS, ME
    [J]. PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 48, 1994, 48 : 143 - 179
  • [6] Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes
    Gall, JG
    Bellini, M
    Wu, Z
    Murphy, C
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (12) : 4385 - 4402
  • [7] The yeast hnRNP-like protein Hrp1/Nab4 marks a transcript for nonsense-mediated mRNA decay
    González, CI
    Ruiz-Echevarría, MJ
    Vasudevan, S
    Henry, MF
    Peltz, SW
    [J]. MOLECULAR CELL, 2000, 5 (03) : 489 - 499
  • [8] Temporal regulation of RNA polymerase II by Srb10 and Kin28 cyclin-dependent kinases
    Hengartner, CJ
    Myer, VE
    Liao, SM
    Wilson, CJ
    Koh, SS
    Young, RA
    [J]. MOLECULAR CELL, 1998, 2 (01) : 43 - 53
  • [9] RNA polymerase II is an essential mRNA polyadenylation factor
    Hirose, Y
    Manley, JL
    [J]. NATURE, 1998, 395 (6697) : 93 - 96
  • [10] Phosphorylated RNA polymerase II stimulates pre-mRNA splicing
    Hirose, Y
    Tacke, R
    Manley, JL
    [J]. GENES & DEVELOPMENT, 1999, 13 (10) : 1234 - 1239