SAGA and a novel Drosophila export complex anchor efficient transcription and mRNA export to NPC

被引:146
作者
Kurshakova, Maria M. [2 ]
Krasnov, Alexey N. [2 ,3 ]
Kopytova, Daria V. [2 ]
Shidlovskii, Yulii V. [2 ]
Nikolenko, Julia V. [2 ]
Nabirochkina, Elena N. [2 ,3 ]
Spehner, Daniele [4 ]
Schultz, Patrick [4 ]
Tora, Laszlo [1 ]
Georgieva, Sofia G. [1 ,2 ,3 ,5 ]
机构
[1] CNRS, Inst Genet Biol Mol Cellulaire, Dept Transcript, UMR 7104, F-67404 Illkirch Graffenstaden, France
[2] Russian Acad Sci, Inst Gene Biol, Dept Reg Gene Express, Moscow, Russia
[3] Univ Oslo, Ctr Med Studies, Moscow, Russia
[4] CNRS, Inst Genet Biol Mol Cellulaire, Illkirch Graffenstaden, France
[5] Russian Acad Sci, Inst Mol Biol, Dept Transcript Factors, Moscow, Russia
关键词
heat shock; nuclear envelope; RNA polymerase II transcription; Sac3; Sus1;
D O I
10.1038/sj.emboj.7601901
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
SAGA/TFTC-type multiprotein complexes play important roles in the regulation of transcription. We have investigated the importance of the nuclear positioning of a gene, its transcription and the consequent export of the nascent mRNA. We show that E(y)2 is a subunit of the SAGA/TFTC-type histone acetyl transferase complex in Drosophila and that E(y)2 concentrates at the nuclear periphery. We demonstrate an interaction between E(y)2 and the nuclear pore complex (NPC) and show that SAGA/TFTC also contacts the NPC at the nuclear periphery. E(y)2 forms also a complex with X-linked male sterile 2 (Xmas-2) to regulate mRNA transport both in normal conditions and after heat shock. Importantly, E(y)2 and Xmas-2 knockdown decreases the contact between the heat-shock protein 70 (hsp70) gene loci and the nuclear envelope before and after activation and interferes with transcription. Thus, E(y)2 and Xmas-2 together with SAGA/TFTC function 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:4956 / 4965
页数:10
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