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The U11-48K Protein Contacts the 5′ Splice Site of U12-Type Introns and the U11-59K Protein

机译:U11-48K蛋白接触U12型内含子和U11-59K蛋白的5剪接位点

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摘要

Little is currently known about proteins that make contact with the pre-mRNA in the U12-dependent spliceosome and thereby contribute to intron recognition. Using site-specific cross-linking, we detected an interaction between the U11-48K protein and U12-type 5′ splice sites (5′ss). This interaction did not require branch point recognition and was sensitive to 5′ss mutations, suggesting that 48K interacts with the 5′ss during the first steps of prespliceosome assembly in a sequence-dependent manner. RNA interference-induced knockdown of 48K in HeLa cells led to reduced cell growth and the inhibition of U12-type splicing, as well as the activation of cryptic, U2-type splice sites, suggesting that 48K plays a critical role in U12-type intron recognition. 48K knockdown also led to reduced levels of U11/U12 di-snRNP, indicating that 48K contributes to the stability and/or formation of this complex. In addition to making contact with the 5′ss, 48K interacts with the U11-59K protein, a protein at the interface of the U11/U12 di-snRNP. These studies provide important insights into the protein-mediated recognition of the U12-type 5′ss, as well as functionally important interactions within the U11/U12 di-snRNP.
机译:目前尚不了解与U12依赖性剪接体中的pre-mRNA接触并因此有助于内含子识别的蛋白质。使用位点特异性交联,我们检测到U11-48K蛋白与U12型5'剪接位点(5'ss)之间的相互作用。该相互作用不需要分支点识别并且对5's突变敏感,表明48K在剪接体组装的第一步中以序列依赖性方式与5's相互作用。 RNA干扰诱导的HeLa细胞48K敲低导致细胞生长减少和U12型剪接的抑制以及隐性U2型剪接位点的激活,表明48K在U12型内含子中起关键作用承认。 48K敲低还导致U11 / U12 di-snRNP水平降低,表明48K有助于该复合物的稳定性和/或形成。除了与5's接触外,48K还与U11-59K蛋白相互作用,该蛋白位于U11 / U12 di-snRNP的界面。这些研究为蛋白质介导的U12型5's识别以及U11 / U12 di-snRNP内部的功能上重要的相互作用提供了重要的见识。

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