首页> 美国卫生研究院文献>Molecular and Cellular Biology >3′ End Processing of Drosophila melanogaster Histone Pre-mRNAs: Requirement for Phosphorylated Drosophila Stem-Loop Binding Protein and Coevolution of the Histone Pre-mRNA Processing System
【2h】

3′ End Processing of Drosophila melanogaster Histone Pre-mRNAs: Requirement for Phosphorylated Drosophila Stem-Loop Binding Protein and Coevolution of the Histone Pre-mRNA Processing System

机译:果蝇组蛋白前mRNA的3末端加工:磷酸化果蝇茎-环结合蛋白的要求和组蛋白前mRNA加工系统的共同进化

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Synthetic pre-mRNAs containing the processing signals encoded by Drosophila melanogaster histone genes undergo efficient and faithful endonucleolytic cleavage in nuclear extracts prepared from Drosophila cultured cells and 0- to 13-h-old embryos. Biochemical requirements for the in vitro cleavage are similar to those previously described for the 3′ end processing of mammalian histone pre-mRNAs. Drosophila 3′ end processing does not require ATP and occurs in the presence of EDTA. However, in contrast to mammalian processing, Drosophila processing generates the final product ending four nucleotides after the stem-loop. Cleavage of the Drosophila substrates is abolished by depleting the extract of the Drosophila stem-loop binding protein (dSLBP), indicating that both dSLBP and the stem-loop structure in histone pre-mRNA are essential components of the processing machinery. Recombinant dSLBP expressed in insect cells by using the baculovirus system efficiently complements the depleted extract. Only the RNA-binding domain plus the 17 amino acids at the C terminus of dSLBP are required for processing. The full-length dSLBP expressed in insect cells is quantitatively phosphorylated on four residues in the C-terminal region. Dephosphorylation of the recombinant dSLBP reduces processing activity. Human and Drosophila SLBPs are not interchangeable and strongly inhibit processing in the heterologous extracts. The RNA-binding domain of the dSLBP does not substitute for the RNA-binding domain of the human SLBP in histone pre-mRNA processing in mammalian extracts. In addition to the stem-loop structure and dSLBP, 3′ processing in Drosophila nuclear extracts depends on the presence of a short stretch of purines located ca. 20 nucleotides downstream from the stem, and an Sm-reactive factor, most likely the Drosophila counterpart of vertebrate U7 snRNP.
机译:包含果蝇组蛋白基因编码的加工信号的合成前mRNA在果蝇培养的细胞和0至13小时大的胚胎制备的核提取物中进行了有效而忠实的内切核酸裂解。体外裂解的生物化学要求类似于先前描述的哺乳动物组蛋白前mRNA 3'末端加工的生物化学要求。果蝇3'末端加工不需要ATP,并且在EDTA存在下发生。但是,与哺乳动物加工相反,果蝇加工产生的最终产物在茎环后终止了四个核苷酸。果蝇底物的切割通过消耗果蝇茎环结合蛋白(dSLBP)的提取物而被取消,这表明组蛋白前mRNA中的dSLBP和茎环结构都是加工机械的重要组成部分。通过使用杆状病毒系统在昆虫细胞中表达的重组dSLBP有效补充了枯竭的提取物。加工仅需要RNA结合结构域和dSLBP C末端的17个氨基酸。在昆虫细胞中表达的全长dSLBP在C端区域的四个残基上被定量磷酸化。重组dSLBP的去磷酸化降低了加工活性。人和果蝇的SLBP不能互换,并且强烈抑制异源提取物中的加工。在哺乳动物提取物中的组蛋白前mRNA加工中,dSLBP的RNA结合结构域不能替代人SLBP的RNA结合结构域。除了茎环结构和dSLBP外,果蝇核提取物中的3'加工还取决于存在大约一小段嘌呤的嘌呤。茎下游20个核苷酸和一个Sm反应因子,很可能是脊椎动物U7 snRNP的果蝇对应物。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号