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C组异质核糖核蛋白与U2小核核糖核蛋白颗粒的5'茎环结合。

The C-group heterogeneous nuclear ribonucleoprotein proteins bind to the 5' stem-loop of the U2 small nuclear ribonucleoprotein particle.

作者信息

Temsamani J, Pederson T

机构信息

Cell Biology Group, Worcester Foundation for Biomedical Research, Shrewsbury, Massachusetts 01545, USA.

出版信息

J Biol Chem. 1996 Oct 4;271(40):24922-6. doi: 10.1074/jbc.271.40.24922.

Abstract

The C-group heterogeneous nuclear ribonucleoprotein (hnRNP) proteins bind to nascent pre-messenger RNA. In vitro studies have indicated that the C hnRNP proteins bind particularly strongly to the intron polypyrimidine tract of pre-mRNA and may be important for pre-mRNA splicing. In addition, there is evidence that the interaction of the C hnRNP proteins with pre-mRNA is facilitated by the U1 and U2 small nuclear RNPs (snRNPs). In the present study, we have uncovered another feature of the C hnRNP proteins that may provide a unifying framework for these previous observations; the C hnRNP proteins bind to the 5' stem-loop of the U2 snRNP. This was detected by incubating human 32P-labeled U2 snRNP in micrococcal nuclease-treated HeLa nuclear extracts, followed by UV-mediated protein-RNA cross-linking, which revealed that C hnRNP proteins were cross-linked to 32P-nucleotides in the U2 snRNP. In similar experiments, no cross-linking of C hnRNP proteins to 32P-labeled U1 or U4 snRNPs was observed. The observed cross-linking of C hnRNP proteins to U2 snRNP was efficiently competed by excess U2 RNA and by poly(U) but not by poly(A). No competition was observed with an RNA molecule comprising U2 nucleotides 105-189, indicating that the C hnRNP protein interactive regions of U2 RNA reside solely in the 5' half of the molecule. Oligodeoxynucleotide-mediated RNase H cleavage experiments revealed that a 5' region of U2 RNA including nucleotides 15-28 is essential for the observed C hnRNP protein cross-linking. C hnRNP protein cross-linking to U2 snRNP was efficiently competed by a mini-RNA corresponding to the first 29 nucleotides of U2 RNA, whereas no competition was observed with a variant of this mini-RNA in which the UUUU loop of stem-loop I was mutationally configured into a single-stranded RNA by replacing the stem with non-pairing nucleotides. Competition experiments with another mutant mini-U2 RNA in which the UUUU loop was replaced by AAAA indicated that both the UUUU loop and the stem are important for C hnRNP protein cross-linking, a finding consistent with other recent data on the RNA sequence specificity of C hnRNP protein binding.

摘要

C组异质核核糖核蛋白(hnRNP)与新生的前体信使RNA结合。体外研究表明,C hnRNP蛋白与前体mRNA的内含子多嘧啶序列结合特别紧密,可能对前体mRNA剪接很重要。此外,有证据表明,U1和U2小核核糖核蛋白(snRNP)促进了C hnRNP蛋白与前体mRNA的相互作用。在本研究中,我们发现了C hnRNP蛋白的另一个特征,这可能为这些先前的观察提供一个统一的框架;C hnRNP蛋白与U2 snRNP的5'茎环结合。这是通过在微球菌核酸酶处理的HeLa核提取物中孵育人32P标记的U2 snRNP,然后进行紫外线介导的蛋白质-RNA交联检测到的,结果显示C hnRNP蛋白与U2 snRNP中的32P核苷酸交联。在类似的实验中,未观察到C hnRNP蛋白与32P标记的U1或U4 snRNP交联。观察到的C hnRNP蛋白与U2 snRNP的交联被过量的U2 RNA和聚(U)有效竞争,但不被聚(A)竞争。用包含U2核苷酸105 - 189的RNA分子未观察到竞争,表明U2 RNA的C hnRNP蛋白相互作用区域仅位于分子的5'半部分。寡脱氧核苷酸介导的RNase H切割实验表明,U2 RNA的5'区域(包括核苷酸15 - 28)对于观察到的C hnRNP蛋白交联至关重要。C hnRNP蛋白与U2 snRNP的交联被对应于U2 RNA前29个核苷酸的小RNA有效竞争,而对于该小RNA的一个变体未观察到竞争,在该变体中,茎环I的UUUU环通过用非配对核苷酸取代茎而突变为单链RNA。用另一个突变小U2 RNA进行的竞争实验,其中UUUU环被AAAA取代,表明UUUU环和茎对于C hnRNP蛋白交联都很重要,这一发现与最近关于C hnRNP蛋白结合的RNA序列特异性的其他数据一致。

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