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

被引:851
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
[21]   Control of cleavage site selection during mRNA 3′ end formation by a yeast hnRNP [J].
Minvielle-Sebastia, L ;
Beyer, K ;
Krecic, AM ;
Hector, RE ;
Swanson, MS ;
Keller, W .
EMBO JOURNAL, 1998, 17 (24) :7454-7468
[22]   MESSENGER-RNA CAPPING ENZYMES FROM EUKARYOTIC CELLS [J].
MIZUMOTO, K ;
KAZIRO, Y .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, 1987, 34 :1-28
[23]   Phospho-carboxyl-terminal domain binding and the role of a prolyl isomerase in pre-mRNA 3′-end formation [J].
Morris, DP ;
Phatnani, HP ;
Greenleaf, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (44) :31583-31587
[24]   Transcription units as RNA processing units [J].
Neugebauer, KM ;
Roth, MB .
GENES & DEVELOPMENT, 1997, 11 (24) :3279-3285
[25]   Mapping chromosomal proteins in vivo by formaldehyde-crosslinked-chromatin immunoprecipitation [J].
Orlando, V .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :99-104
[26]   Analysis of chromatin structure by in vivo formaldehyde cross-linking [J].
Orlando, V ;
Strutt, H ;
Paro, R .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1997, 11 (02) :205-214
[27]   Growth-related changes in phosphorylation of yeast RNA polymerase II [J].
Patturajan, M ;
Schulte, RJ ;
Sefton, BM ;
Berezney, R ;
Vincent, M ;
Bensaude, O ;
Warren, SL ;
Corden, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (08) :4689-4694
[28]   Recombinant human mRNA cap methyltransferase binds capping enzyme RNA polymerase IIo complexes [J].
Pillutla, RC ;
Yue, ZY ;
Maldonado, E ;
Shatkin, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :21443-21446
[29]   IN-VIVO TRANSCRIPTIONAL PAUSING AND CAP FORMATION ON 3 DROSOPHILA HEAT-SHOCK GENES [J].
RASMUSSEN, EB ;
LIS, JT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7923-7927
[30]   Kin28, the TFIIH-associated carboxy-terminal domain kinase, facilitates the recruitment of mRNA processing machinery to RNA polymerase II [J].
Rodriguez, CR ;
Cho, EJ ;
Keogh, MC ;
Moore, CL ;
Greenleaf, AL ;
Buratowski, S .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (01) :104-112