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Complex splicing control of the human thrombopoietin gene by intronic G runs

机译:内含子G运行对人类血小板生成素基因的复杂剪接控制

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摘要

The human thrombopoietin (THPO) gene displays a series of alternative splicing events that provide valuable models for studying splicing mechanisms. The THPO region spanning exon 1-4 presents both alternative splicing of exon 2 and partial intron 2 (IVS2) retention following the activation of a cryptic 3' splice site 85 nt upstream of the authentic acceptor site. IVS2 is particularly rich in stretches of 3-5 guanosines (namely, G1-G10) and we have characterized the role of these elements in the processing of this intron. In vivo studies show that runs G7-G10 work in a combinatorial way to control the selection of the proper 3' splice site. In particular, the G7 element behaves as the splicing hub of intron 2 and its interaction with hnRNP H1 is critical for the splicing process. Removal of hnRNP H1 by RNA interference promoted the usage of the cryptic 3' splice site so providing functional evidence that this factor is involved in the selection of the authentic 3' splice site of THPO IVS2.
机译:人类血小板生成素(THPO)基因显示了一系列的选择性剪接事件,为研究剪接机制提供了有价值的模型。跨越外显子1-4的THPO区在激活真实受体位点上游的3'隐含剪接位点85 nt之后,激活了外显子2的可变剪接和部分内含子2(IVS2)保留。 IVS2在3-5个鸟苷(即G1-G10)中特别丰富,我们已经表征了这些元素在加工该内含子中的作用。体内研究表明,运行G7-G10以组合方式起作用,以控制正确3'剪接位点的选择。特别地,G7元件充当内含子2的剪接中心,并且它与hnRNP H1的相互作用对于剪接过程至关重要。 RNA干扰去除hnRNP H1促进了隐性3'剪接位点的使用,因此提供了功能证据,表明该因素与THPO IVS2真实3'剪接位点的选择有关。

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