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Regulation of SRp20 exon 4 splicing

机译:SRp20外显子4剪接的调控

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摘要

SR proteins are essential splicing factors involved in the use of both constitutive and alternative exons. We previously showed that the SR proteins SRp20 and ASF/SF2 have antagonistic activities on SRp20 pre-mRNA splicing. SRp20 activates exon 4 recognition in its pre-mRNA, whereas ASF/SF2 inhibits this recognition. In experiments aimed at testing the specificity of SRp20 and ASF/SF2 for exon 4 splicing regulation, we show here that this specificity lies in the RNA binding domains of SRp20 and ASF/SF2 and not in the RS domains. Surprisingly, a deletion of 14 amino acids at the end of ASF/SF2-RBD2 converts ASF/SF2 from an inhibitor to an activator of exon 4 splicing. We found that ASF3 also inhibits exon 4 recognition, thus acting similarly to ASF/SF2, while SC35 activates a cryptic 5' splice site downstream of exon 3 and, in doing so, represses exon 4 use. In contrast, Tra2 and the SR proteins 9G8 and SRp40 do not appear to affect exon 4 splicing.
机译:SR蛋白是组成型和替代性外显子使用中必不可少的剪接因子。我们以前表明SR蛋白SRp20和ASF / SF2对SRp20 pre-mRNA剪接具有拮抗活性。 SRp20激活其前mRNA中的外显子4识别,而ASF / SF2抑制该识别。在旨在测试SRp20和ASF / SF2对外显子4剪接调控的特异性的实验中,我们在这里表明,这种特异性在于SRp20和ASF / SF2的RNA结合结构域,而不在于RS结构域。令人惊讶地,在ASF / SF2-RBD2末端缺失14个氨基酸将ASF / SF2从抑制剂转变为外显子4剪接的活化剂。我们发现,ASF3还抑制外显子4的识别,从而起到与ASF / SF2类似的作用,而SC35激活外显子3下游的隐蔽5'剪接位点,从而抑制外显子4的使用。相反,Tra2和SR蛋白9G8和SRp40似乎不影响外显子4的剪接。

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