CWC22 Connects Pre-mRNA Splicing and Exon Junction Complex Assembly

被引:93
作者
Steckelberg, Anna-Lena [1 ]
Boehm, Volker [1 ]
Gromadzka, Agnieszka M. [1 ]
Gehring, Niels H. [1 ]
机构
[1] Univ Cologne, Inst Genet, D-50674 Cologne, Germany
关键词
CRYSTAL-STRUCTURE; CORE COMPLEX; SPLICEOSOME; REVEALS;
D O I
10.1016/j.celrep.2012.08.017
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The exon junction complex (EJC) is a key regulator of posttranscriptional mRNA fate and binds to mRNA during splicing. Although the composition of EJCs is well understood, the mechanism mediating splicing-dependent EJC assembly and the factor(s) recruiting the EJC remain elusive. Here, we identify CWC22 as an essential splicing factor that is required for EJC assembly. In CWC22-depleted cells, pre-mRNA splicing is impaired but is rescued by a central fragment of CWC22. We show that the MIF4G domain of CWC22 initiates EJC assembly via a direct interaction with the EJC core protein eIF4A3, and we characterize mutations in eIF4A3 that abolish binding to CWC22. These eIF4A3 mutants efficiently nucleate splicing-independent recombinant EJC core complexes, but they fail to support splicing-dependent EJC deposition. Our work establishes a direct link between the splicing machinery and the EJC, hence uncovering a molecular interaction at the center of a posttranscriptional gene regulation network.
引用
收藏
页码:454 / 461
页数:8
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