Inhibition of splicing and nuclear retention of pre-mRNA by spliceostatin A in fission yeast

被引:27
|
作者
Lo, Chor-Wai
Kaida, Daisuke
Nishimura, Shinichi
Matsuyama, Akihisa
Yashiroda, Yoko
Taoka, Hiroshi
Ishigami, Ken
Watanabe, Hidenori
Nakajima, Hidenori
Tani, Toklo
Horinouchi, Sueharu
Yoshida, Minoru
机构
[1] RIKEN, Chem Genet Lab, Wako, Saitama 3510198, Japan
[2] Univ Tokyo, Dept Biotechnol, Bunkyo Ku, Tokyo 1138657, Japan
[3] Univ Tokyo, Dept Appl Biol Chem, Bunkyo Ku, Tokyo 1138657, Japan
[4] Astellas Pharma Inc, Fermentat Res Labs, Tsukuba, Ibaraki 3002698, Japan
[5] Kumamoto Univ, Grad Sch Sci & Technol, Dept Biol Sci, Kumamoto 8608555, Japan
[6] CREST, Japan Sci & Technol Corp, Res Project, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
spliceostatin a; fission yeast; pre-mRNA; SF3b; splicing; pre-mRNA retention;
D O I
10.1016/j.bbrc.2007.10.029
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
Nuclear retention of pre-mRNAs is tightly regulated by several security mechanisms that prevent pre-mRNA export into the cytoplasm. Recently, spliceostatin A, a methylated derivative of a potent antitumor microbial metabolite FR901464, was found to cause pre-mRNA accumulation and translation in mammalian cells. Here we report that spliceostatin A also inhibits splicing and nuclear retention of pre-mRNA in a fission yeast strain that lacks the multidrug resistance protein Pmd1. As observed in mammalian cells, spliceostatin A is bound to components of the SF3b complex in the spliceosome. Furthermore, overexpression of nup211, a homolog of Saccharomyces cerevisiae MLP1, suppresses translation of pre-mRNAs accumulated by spliceostatin A. These results suggest that the SF3b complex has a conserved role in pre-mRNA retention, which is independent of the Mlp1 function. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:573 / 577
页数:5
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