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Two different RNA binding activities for the All-rich element and the poly(A) sequence of the mouse neuronal protein mHuC

机译:小鼠神经元蛋白mHuC的All-rich元素和poly(A)序列的两种不同的RNA结合活性

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HuC is one of the RNA binding proteins which are suggested to play important roles in neuronal differentiation and maintenance. We cloned and sequenced cDNAs encoding a mouse protein which is homologous to human HuC (hHuC). The longest cDNA encodes a367 amino acid protein with three RNA recognition motifs (RRMs) and displays 96% identity to hHuC. Northern blot analysis showed that two different mRNAs, of 5.3 and 4.3 kb, for mouse HuC (mHuC) are expressed specifically in brain tissue. Comparison of cDNA sequences with the corresponding genomic sequence revealed that alternative 3' splice site selection generates two closely related mHuC iso-forms. Iterative in vitro RNA selection and binding analyses showed that both HuC isoforms can bind with almost identical specificity to sequences similar to the AU-rich element (ARE), which is involved in the regulation of mRNA stability. Functional domain mapping using mHuC deletion mutants showed that the first RRM binds to ARE, that the second RRM has no RNA binding activity by itself, but facilitates ARE binding by the first RRM and that the third RRM has specific binding activity for the poly(A) sequence.
机译:HuC是RNA结合蛋白之一,被认为在神经元分化和维持中起重要作用。我们克隆和测序编码与人类HuC(hHuC)同源的小鼠蛋白质的cDNA。最长的cDNA编码具有三个RNA识别基序(RRM)的a367氨基酸蛋白,并与hHuC显示96%的同一性。 Northern印迹分析表明,小鼠HuC(mHuC)的两种不同的mRNA(分别为5.3和4.3 kb)在脑组织中表达。 cDNA序列与相应的基因组序列的比较表明,备选的3'剪接位点选择产生两个密切相关的mHuC同种型。体外迭代RNA选择和结合分析表明,两种HuC亚型都可以与几乎与富含AU的元件(ARE)相似的序列结合,后者参与调控mRNA的稳定性。使用mHuC缺失突变体进行的功能域定位显示,第一个RRM与ARE结合,第二个RRM本身没有RNA结合活性,但是促进了第一个RRM的ARE结合,并且第三个RRM对poly(A ) 顺序。

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