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首页> 外文期刊>Nucleic acids research >Formation of the yeast splicing complex A1 and association of the splicing factor PRP19 with the pre-mRNA are independent of the 3′ region of the intron
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Formation of the yeast splicing complex A1 and association of the splicing factor PRP19 with the pre-mRNA are independent of the 3′ region of the intron

机译:酵母剪接复合物A1的形成以及剪接因子PRP19与前mRNA的结合均独立于内含子的3'区

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Assembly of the spliceosome is a step-wise process and involves squential binding of snRNAs to the pre-mRNA to form pre-splicing complex A2-1. Subsequent dissociation of U4 from the spliceosome is accompanied by formation of complex A1 (Genes Dev. 1, 1014–1027, 1987). We show that the 3′ region of the intron sequence is not required for efficient assembly of the yeast spliceosome. Truncated precursor mRNA retaining only four or five nucleotides 3′ to the TACTAAC box formed pre-splicing complex A1, kinetically the last pre-mRNA containing splicing complex identified. The subsequent cleavage–ligation reaction requires at least 23 nucleotides on the 3′ side of the TACTAAC box in a sequence-independent manner. Immunoprecipitation with anti-PRP19 antibody showed that association of PRP19 with the spliceosome was also independent of the 3′ region of the intron.
机译:剪接体的组装是一个逐步的过程,涉及到snRNA与pre-mRNA的顺序结合,以形成pre-splicing复合体A2-1。随后U4从剪接体上解离,伴随着复合物A1的形成(Genes Dev。1,1014-1027,1987)。我们显示,内含子序列的3'区域对于酵母剪接体的有效组装不是必需的。截短的前体mRNA仅保留了TACTAAC框3'的四个或五个核苷酸,形成了预剪接复合物A1,从动力学上讲,这是最后鉴定的含mRNA的剪接复合物。随后的切割-连接反应需要在TACTAAC盒的3'侧以序列无关的方式至少包含23个核苷酸。抗PRP19抗体的免疫沉淀表明PRP19与剪接体的缔合也独立于内含子的3'区。

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