The Wilms' tumor 1 (WT1) gene (+KTS isoform) functions with a CTE to enhance translation from an unspliced RNA with a retained intron

被引:72
作者
Bor, Yeou-cherng
Swartz, Jennifer
Morrison, Avril
Rekosh, David
Ladomery, Michael
Hammarskjold, Marie-Louise [1 ]
机构
[1] Univ Virginia, Myles H Thaler Ctr AIDS & Human Retrovirus Res, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
[3] Univ W England, Bristol Genom Res Inst, Ctr Res Biomed, Bristol BS16 1QY, Avon, England
关键词
WT1; Wilms' tumor; CTE; constitutive transport element; RNA export; post-transcriptional regulation; translational regulation;
D O I
10.1101/gad.1402306
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Wilms' tumor 1 (WT1) gene plays an important role in mammalian urogenital development, and dysregulation of this gene is observed in many human cancers. Alternative splicing of WT1 RNA leads to the expression of two major protein isoforms, WT1(+KTS) and WT1(-KTS). Whereas WT1(-KTS) acts as a transcriptional regulator, no clear function has been ascribed to WT1(+KTS), despite the fact that this protein is crucial for normal development. Here we show that WT1(+KTS) functions to enhance expression from RNA possessing a retained intron and containing either a cellular or viral constitutive transport element (CTE). WT1(+KTS) expression increases the levels of unspliced RNA containing a CTE and specifically promotes the association of this RNA with polyribosomes. These studies provide further support for links between different steps in RNA metabolism and for the existence of post-transcriptional operons.
引用
收藏
页码:1597 / 1608
页数:12
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