Conservative E(y)2/Sus1 protein is the member of SAGA complex and new nuclear pore-associated complex in Drosophila

被引:0
作者
Kurshakova, M. M. [1 ]
Kopytova, D. V. [1 ]
Nabirochkina, E. N. [1 ,2 ]
Nikolenko, Yu. V. [1 ]
Shidlovskii, Yu. V. [1 ]
Georgieva, S. G. [1 ,2 ,3 ]
Krasnov, A. N. [1 ,2 ]
机构
[1] Russian Acad Sci, Inst Gene Biol, Moscow 119334, Russia
[2] Univ Oslo, Ctr Med Studies, Moscow 119334, Russia
[3] Russian Acad Sci, Engelhardt Inst Mol Biol, Moscow 119991, Russia
基金
俄罗斯基础研究基金会;
关键词
RNA EXPORT MACHINERY; MESSENGER-RNA; YEAST GENE; MELANOGASTER; CHROMOSOMES; ACTIVATION; EXPRESSION;
D O I
10.1134/S1022795409100044
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The SGA/TFC complex plays an important role in the regulation of transcription. We have examined the significance of the gene positioning in the nucleus for its transcription and subsequent export of nascent mRNA. It was demonstrated that E(y)2 protein was a subunit of the SAGA/TFTC histone acetyl transferase complex in Drosophila and that E(y)2 concentrated at the nuclear periphery. An interaction between E(y)2 and the nuclear pore complex (NPC) was demonstrated, as well as that SAGA/TFTC also contacted the NPC at nuclear periphery. In addition, it was shown that NPC formed complex with the Xmas-2 protein (X-linked male sterile 2) both in normal conditions and after heat shock. Importantly, the E(y)2 and Xmas-2 knockdown decreased the contact between the heat-shock protein 70 (hsp70) gene loci and the nuclear envelope before and after activation, which interfered with the transcription. Thus, E(y)2 and Xmas-2 together with SAGA/TFTC functioned in the anchoring of a subset of transcription sites to the NPCs to achieve efficient transcription and mRNA export.
引用
收藏
页码:1174 / 1181
页数:8
相关论文
共 22 条
[1]   Use of double-stranded RNA interference in Drosophila cell lines to dissect signal transduction pathways [J].
Clemens, JC ;
Worby, CA ;
Simonson-Leff, N ;
Muda, M ;
Maehama, T ;
Hemmings, BA ;
Dixon, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6499-6503
[2]   Nuclear compartments and gene regulation [J].
Cockell, M ;
Gasser, SM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (02) :199-205
[3]   Transcription factor TFIID recruits factor CPSF for formation of 3' end of mRNA [J].
Dantonel, JC ;
Murthy, KGK ;
Manley, JL ;
Tora, L .
NATURE, 1997, 389 (6649) :399-402
[4]   The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores [J].
Fischer, T ;
Strässer, K ;
Rácz, A ;
Rodriguez-Navarro, S ;
Oppizzi, M ;
Ihrig, P ;
Lechner, J ;
Hurt, E .
EMBO JOURNAL, 2002, 21 (21) :5843-5852
[5]  
Gallardo M, 2001, GENETICS, V157, P79
[6]  
GEORGIEV PG, 1994, GENETICS, V138, P733
[7]   Two novel Drosophila TAFIIs have homology with human TAFII30 and are differentially regulated during development [J].
Georgieva, S ;
Kirschner, DB ;
Jagla, T ;
Nabirochkina, E ;
Hanke, S ;
Schenkel, H ;
De Lorenzo, C ;
Sinha, P ;
Jagla, K ;
Mechler, B ;
Tora, L .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1639-1648
[8]   The novel transcription factor e(y)2 interacts with TAFII40 and potentiates transcription activation on chromatin templates [J].
Georgieva, S ;
Nabirochkina, E ;
Dilworth, FJ ;
Eickhoff, H ;
Becker, P ;
Tora, L ;
Georgiev, P ;
Soldatov, A .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (15) :5223-5231
[9]  
Hediger F, 2004, METHOD ENZYMOL, V375, P345
[10]   Chromatin boundaries in budding yeast: The nuclear pore connection [J].
Ishii, K ;
Arib, G ;
Lin, C ;
Van Houwe, G ;
Laemmli, UK .
CELL, 2002, 109 (05) :551-562