Repeat-Specific Functions for the C-Terminal Domain of RNA Polymerase II in Budding Yeast

被引:5
作者
Babokhov, Michael [1 ]
Mosaheb, Mohammad M. [1 ]
Baker, Richard W. [2 ]
Fuchs, Stephen M. [1 ]
机构
[1] Tufts Univ, Dept Biol, Medford, MA 02155 USA
[2] Univ Calif San Diego, Sch Med, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
关键词
RNA polymerase; transcriptional regulation; tandem repeat domains; HISTONE H3K36 METHYLATION; SACCHAROMYCES-CEREVISIAE; LARGEST SUBUNIT; TRANSCRIPTION ELONGATION; INITIATION COMPLEX; FISSION YEAST; CTD CODE; MEDIATOR; PHOSPHORYLATION; MUTATIONS;
D O I
10.1534/g3.118.200086
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The C-terminal domain (CTD) of the largest subunit of RNA polymerase II (RNAPII) is required to regulate transcription and to integrate it with other essential cellular processes. In the budding yeast Saccharomyces cerevisiae, the CTD of Rpb1p consists of 26 conserved heptad repeats that are post-translationally modified to orchestrate protein factor binding at different stages of the transcription cycle. A long-standing question in the study of the CTD is if there are any functional differences between the 26 repeats. In this study, we present evidence that repeats of identical sequence have different functions based on their position within the CTD. We assembled plasmids expressing Rpb1p with serine to alanine substitutions in three defined regions of the CTD and measured a range of phenotypes for yeast expressing these constructs. Mutations in the beginning and middle regions of the CTD had drastic, and region-specific effects, while mutating the distal region had no observable phenotype. Further mutational analysis determined that Ser5 within the first region of repeats was solely responsible for the observed growth differences and sequencing fast-growing suppressors allowed us to further define the functional regions of the CTD. This mutational analysis is consistent with current structural models for how the RNAPII holoenzyme and the CTD specifically would reside in complex with Mediator and establishes a foundation for studying regioselective binding along the repetitive RNAPII CTD.
引用
收藏
页码:1593 / 1601
页数:9
相关论文
共 47 条
[1]  
Adams A., 1997, METHODS YEAST GENETI
[2]  
Archambault J, 1996, GENETICS, V142, P737
[3]   GENETIC-ANALYSIS OF THE REPETITIVE CARBOXYL-TERMINAL DOMAIN OF THE LARGEST SUBUNIT OF MOUSE RNA POLYMERASE-II [J].
BARTOLOMEI, MS ;
HALDEN, NF ;
CULLEN, CR ;
CORDEN, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (01) :330-339
[4]   RNA Polymerase II C-Terminal Domain: Tethering Transcription to Transcript and Template [J].
Corden, Jeffry L. .
CHEMICAL REVIEWS, 2013, 113 (11) :8423-8455
[5]   The RNA Polymerase II Carboxy-Terminal Domain (CTD) Code [J].
Eick, Dirk ;
Geyer, Matthias .
CHEMICAL REVIEWS, 2013, 113 (11) :8456-8490
[6]   Structure of an mRNA capping enzyme bound to the phosphorylated carboxy-terminal domain of RNA polymerase II [J].
Fabrega, C ;
Shen, V ;
Shuman, S ;
Lima, CD .
MOLECULAR CELL, 2003, 11 (06) :1549-1561
[7]   CTD KINASE ASSOCIATED WITH YEAST RNA POLYMERASE-II INITIATION FACTOR-B [J].
FEAVER, WJ ;
GILEADI, O ;
LI, Y ;
KORNBERG, RD .
CELL, 1991, 67 (06) :1223-1230
[8]   Capping, splicing, and 3′ processing are independently stimulated by RNA polymerase II:: different functions for different segments of the CTD [J].
Fong, N ;
Bentley, DL .
GENES & DEVELOPMENT, 2001, 15 (14) :1783-1795
[9]   Protein modifications in transcription elongation [J].
Fuchs, Stephen M. ;
Laribee, R. Nicholas ;
Strahl, Brian D. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2009, 1789 (01) :26-36
[10]   The cryo-electron microscopy structure of human transcription factor IIH [J].
Greber, Basil J. ;
Nguyen, Thi Hoang Duong ;
Fang, Jie ;
Afonine, Pavel V. ;
Adams, Paul D. ;
Nogales, Eva .
NATURE, 2017, 549 (7672) :414-+