Two subunits specific to the PBAP chromatin remodeling complex have distinct and redundant functions during Drosophila development

被引:34
作者
Carrera, Ines [1 ,2 ]
Zavadil, Jiri [3 ]
Treisman, Jessica E. [1 ,2 ]
机构
[1] NYU, Sch Med, Skirball Inst, Kimmel Ctr Biol & Med, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1128/MCB.00747-08
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
Chromatin remodeling complexes control the availability of DNA binding sites to transcriptional regulators. Two distinct conserved forms of the SWI/SNF class of complexes are characterized by the presence of specific accessory subunits. In Drosophila, the core Brahma complex associates either with Osa to form the BAP complex or with Bap170 and Bap180 to form the PBAP complex. osa mutations reproduce only a subset of the developmental phenotypes caused by mutations in subunits of the core complex. To test whether the PBAP complex performs the remaining functions, we generated mutations in bap170 and bap180. Surprisingly, we found that Bap180 is not essential for viability, although it is required in ovarian follicle cells for normal eggshell development. Bap170 is necessary to stabilize the Bap180 protein, but a mutant form that retains this function is sufficient for both survival and fertility. The two subunits act redundantly to allow metamorphosis; using gene expression profiling of bap170 bap180 double mutants, we found that the PBAP complex regulates genes involved in tissue remodeling and immune system function. Finally, we generated mutants lacking Bap170, Bap180, and Osa in the germ line to demonstrate that the core Brahma complex can function in oogenesis without any of these accessory subunits.
引用
收藏
页码:5238 / 5250
页数:13
相关论文
共 77 条
[11]   Chromatin remodeling: insights and intrigue from single-molecule studies [J].
Cairns, Bradley R. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (11) :989-996
[12]   The nuclear location and chromatin organization of active chorion amplification origins [J].
Calvi, BR ;
Spradling, AC .
CHROMOSOMA, 2001, 110 (03) :159-172
[13]   Distinct roles for the RSC and Swi/Snf ATP-dependent chromatin remodelers in DNA double-strand break repair [J].
Chai, B ;
Huang, J ;
Cairns, BR ;
Laurent, BC .
GENES & DEVELOPMENT, 2005, 19 (14) :1656-1661
[14]   The transcriptional coactivator SAYP is a trithorax group signature subunit of the PBAP chromatin remodeling complex [J].
Chalkley, Gillian E. ;
Moshkin, Yuri M. ;
Langenberg, Karin ;
Bezstarosti, Karel ;
Blastyak, Andras ;
Gyurkovics, Henrik ;
Demmers, Jeroen A. A. ;
Verrijzer, C. Peter .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (09) :2920-2929
[15]   Polybromo-1-bromodomains bind histone H3 at specific acetyl-lysine positions [J].
Chandrasekaran, Renu ;
Thompson, Martin .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 355 (03) :661-666
[16]   Developmental gene amplification: insights into DNA replication and gene expression [J].
Claycomb, JM ;
Orr-Weaver, TL .
TRENDS IN GENETICS, 2005, 21 (03) :149-162
[17]   Osa associates with the Brahma chromatin remodeling complex and promotes the activation of some target genes [J].
Collins, RT ;
Furukawa, T ;
Tanese, N ;
Treisman, JE .
EMBO JOURNAL, 1999, 18 (24) :7029-7040
[18]   Osa-containing Brahma chromatin remodeling complexes are required for the repression of Wingless target genes [J].
Collins, RT ;
Treisman, JE .
GENES & DEVELOPMENT, 2000, 14 (24) :3140-3152
[19]   Transcription factors and nuclear receptors interact with the SWI/SNF complex through the BAF60c subunit [J].
Debril, MB ;
Gelman, L ;
Fayard, E ;
Annicotte, JS ;
Rocchi, S ;
Auwerx, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (16) :16677-16686
[20]  
Elfring LK, 1998, GENETICS, V148, P251