Biochemical function of female-lethal (2)D/Wilms' tumor suppressor-1-associated proteins in alternative pre-mRNA splicing

被引:79
作者
Ortega, A
Niksic, M
Bachi, A
Wilm, M
Sánchez, L
Hastie, N
Valcárcel, J
机构
[1] European Mol Biol Lab, Gene Express Programme, Heidelberg, Germany
[2] MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland
[3] EMBL, Biochem Instrumentat Programme, Heidelberg, Germany
[4] CSIC, Ctr Invest Biol, E-28006 Madrid, Spain
关键词
D O I
10.1074/jbc.M210737200
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
Genetic and molecular data have implicated the Drosophila gene female-lethal (2)d (fl (2)d) in alternative splicing regulation of genes involved in sexual determination. Sex-specific splicing is under the control of the female-specific regulatory protein sex-lethal (SXL). Co-immunoprecipitation and mass spectrometry results indicate that SXL and FL (2)D form a complex and that the protein VIRILIZER and a Ran-binding protein implicated in protein nuclear import are also present in complexes containing FL (2)D. A human homolog of FL (2)D was identified and cloned. Interestingly, this gene encodes a protein (WTAP) that was previously found to interact with the Wilms' tumor suppressor-1 (WT1), an isoform of which binds to and co-localizes with splicing factors. Alternative splicing of transformer pre-mRNA, a target of SXL regulation, was affected by immunodepletion of hFL (2)D/WTAP from HeLa nuclear extracts, thus arguing for a biochemical function of FL (2)D/WTAP proteins in splicing regulation.
引用
收藏
页码:3040 / 3047
页数:8
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