Enzymatic modules of the SAGA chromatin-modifying complex play distinct roles in Drosophila gene expression and development

被引:40
作者
Li, Xuanying [1 ,2 ]
Seidel, Christopher W. [1 ]
Szerszen, Leanne T. [1 ]
Lange, Jeffrey J. [1 ]
Workman, Jerry L. [1 ]
Abmayr, Susan M. [1 ,2 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
[2] Univ Kansas, Dept Anat & Cell Biol, Med Ctr, Kansas City, KS 66160 USA
关键词
SAGA complex; deubiquitinase module; embryogenesis; transcription; DOMINANT CEREBELLAR-ATAXIA; MESSENGER-RNA EXPORT; HISTONE ACETYLTRANSFERASE; TRANSCRIPTION COACTIVATOR; NEURONAL CONNECTIVITY; RETINAL DEGENERATION; H2B DEUBIQUITINATION; ACETYLASE COMPLEX; ADA2; HOMOLOGS; GCN5;
D O I
10.1101/gad.300988.117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Spt-Ada-Gcn5-acetyltransferase (SAGA) chromatin-modifying complex is a transcriptional coactivator that contains four different modules of subunits. The intact SAGA complex has been well characterized for its function in transcription regulation and development. However, little is known about the roles of individual modules within SAGA and whether they have any SAGA-independent functions. Here we demonstrate that the two enzymatic modules of Drosophila SAGA are differently required in oogenesis. Loss of the histone acetyltransferase (HAT) activity blocks oogenesis, while loss of the H2B deubiquitinase (DUB) activity does not. However, the DUB module regulates a subset of genes in early embryogenesis, and loss of the DUB subunits causes defects in embryogenesis. ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-throughput sequencing) analysis revealed that both the DUB and HAT modules bind most SAGA target genes even though many of these targets do not require the DUB module for expression. Furthermore, we found that the DUB module can bind to chromatin and regulate transcription independently of the HAT module. Our results suggest that the DUB module has functions within SAGA and independent functions.
引用
收藏
页码:1588 / 1600
页数:13
相关论文
共 70 条
[1]   Identification and distinct regulation of yeast TATA box-containing genes [J].
Basehoar, AD ;
Zanton, SJ ;
Pugh, BF .
CELL, 2004, 116 (05) :699-709
[2]   The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription [J].
Bonnet, Jacques ;
Wang, Chen-Yi ;
Baptista, Tiago ;
Vincent, Stephane D. ;
Hsiao, Wei-Chun ;
Stierle, Matthieu ;
Kao, Cheng-Fu ;
Tora, Laszlo ;
Devys, Didier .
GENES & DEVELOPMENT, 2014, 28 (18) :1999-2012
[3]   Developmental control of nuclear size and shape by kugelkern and kurzkern [J].
Brandt, A ;
Papagiannouli, F ;
Wagner, N ;
Wilsch-Bräuninger, M ;
Braun, M ;
Furlong, EE ;
Loserth, S ;
Wenzl, C ;
Pilot, F ;
Vogt, N ;
Lecuit, T ;
Krohne, G ;
Grosshans, J .
CURRENT BIOLOGY, 2006, 16 (06) :543-552
[4]   A function for kinesin I in the posterior transport of oskar mRNA and Staufen protein [J].
Brendza, RP ;
Serbus, LR ;
Duffy, JB ;
Saxton, WM .
SCIENCE, 2000, 289 (5487) :2120-2122
[5]   Tetrahymena histone acetyltransferase A: A homolog to yeast Gcn5p linking histone acetylation to gene activation [J].
Brownell, JE ;
Zhou, JX ;
Ranalli, T ;
Kobayashi, R ;
Edmondson, DG ;
Roth, SY ;
Allis, CD .
CELL, 1996, 84 (06) :843-851
[6]   Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos [J].
Bu, Ping ;
Evrard, Yvonne A. ;
Lozano, Guillermina ;
Dent, Sharon Y. R. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (09) :3405-3416
[7]   Drosophila Stem Cells Share a Common Requirement for the Histone H2B Ubiquitin Protease Scrawny [J].
Buszczak, Michael ;
Paterno, Shelley ;
Spradling, Allan C. .
SCIENCE, 2009, 323 (5911) :248-251
[8]   SAGA DUB-Ubp8 Deubiquitylates Centromeric Histone Variant Cse4 [J].
Canzonetta, Claudia ;
Vernarecci, Stefano ;
Iuliani, Michele ;
Marracino, Cristina ;
Belloni, Claudia ;
Ballario, Paola ;
Filetici, Patrizia .
G3-GENES GENOMES GENETICS, 2016, 6 (02) :287-298
[9]   The histone H3 acetylase dGcn5 is a key player in Drosophila melanogaster metamorphosis [J].
Carré, C ;
Szymczak, D ;
Pidoux, J ;
Antoniewski, C .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (18) :8228-8238
[10]   A global change in RNA polymerase II pausing during the Drosophila midblastula transition [J].
Chen, Kai ;
Johnston, Jeff ;
Shao, Wanqing ;
Meier, Samuel ;
Staber, Cynthia ;
Zeitlinger, Julia .
ELIFE, 2013, 2