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Alternative splicing is an important process contributing to proteome diversity without involving an increase in the number of genes. In some cases, alternative splicing is carried out under 'trans-mode', called alternative trans-splicing, in which exons located on separate pre-mRNA molecules are selectively joined to produce mature mRNAs encoding proteins with distinct structures and functions. However, it is not known how widespread or how frequently trans-splicing occurs in vivo. Recently, trans-allelic trans-splicing has been unambiguously demonstrated in Drosophila using a SNP (single nucleotide polymorphism) as a marker. In this review, we provide an overview of alternative trans-splicing in Drosophila and mammals, and discuss its mechanisms.  相似文献   

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Alternative splicing is used by metazoans to increase protein diversity and to alter gene expression during development. However, few factors that control splice site choice in vivo have been identified. Here we describe a factor, Half pint (Hfp), that regulates RNA splicing in Drosophila. Females harboring hypomorphic mutations in hfp lay short eggs and show defects in germline mitosis, nuclear morphology, and RNA localization during oogenesis. We find that hfp encodes the Drosophila ortholog of human PUF60 and functions in both constitutive and alternative splicing in vivo. In particular, hfp mutants display striking defects in the developmentally regulated splicing of ovarian tumor (otu). Furthermore, transgenic expression of the missing otu splice form can rescue the ovarian phenotypes of hfp.  相似文献   

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Alternative splicing: increasing diversity in the proteomic world   总被引:45,自引:0,他引:45  
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Graveley BR 《Cell》2002,109(4):409-412
Alternative splicing is an important means of regulating the expression of eukaryotic genes and enhancing protein diversity. A detailed examination of the Drosophila Sex-lethal gene has led to two significant discoveries-the role of the splicing factor SPF45 in defining the site of exon ligation, and that alternative splicing can be regulated at the second step.  相似文献   

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可变剪接是生物重要的转录后修饰过程,是转录组和蛋白组多样性的重要来源.可变剪接参与了植物众多生理过程,包括植物昼夜节律、生长发育等,在植物响应生物和非生物胁迫过程中尤为普遍.近年来,可变剪接被认为是植物抵御病原菌侵染的重要调控机制.本文综述了可变剪接在植物免疫各个层面的调控作用,包括调节重要免疫受体、R基因、激素信号路...  相似文献   

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Alternative splicing of mRNA allows many gene products with different functions to be produced from a single coding sequence. Exon skipping is the most commonly known alternative splicing mechanism. A comprehensive database of alternative splicing by exon skipping is made available for the human genome data. 1,229 human genes are identified to exhibit alternative splicing by exon skipping. Availability: http://sege.ntu.edu.sg/wester/ashes/.  相似文献   

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癌症与可变剪接   总被引:2,自引:0,他引:2  
高亚梅  韩毅强 《生物技术通讯》2007,18(6):1016-1018,1049
可变剪接在发育、分化和癌症等过程中发挥着非常重要的作用。近年来,越来越多的研究表明可变剪接与癌症有着密切的关系,许多癌症相关基因受可变剪接调控。由于癌症特异性的剪接变体具有明显的诊断价值,使得对癌症与可变剪接的研究成为热点。简要概述了癌症相关基因的可变剪接、可变剪接变体的鉴定方法、可变剪接与癌症治疗等研究进展。  相似文献   

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Alternative pre-mRNA splicing, which produces various mRNA isoforms with distinct structures and functions from a single gene, is regulated by specific RNA-binding proteins and is an essential method for regulating gene expression in mammals. Recent studies have shown that abnormal change during neuronal development triggered by splicing mis-regulation is an important feature of various neurological diseases. Polypyrimidine tract binding protein 1 (PTBP1) is a kind of RNA-binding proteins with extensive biological functions. As a well-known splicing regulator, it affects the neuronal development process through its involvement in axon formation, synaptogenesis, and neuronal apoptosis, according to the most recent studies. Here, we summarized the mechanism of alternative splicing, structure and function of PTBP1, and the latest research progress on the role of alternative splicing events regulated by PTBP1 in axon formation, synaptogenesis and neuronal apoptosis, to reveal the mechanism of PTBP1-regulated changes in neuronal development process.  相似文献   

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可变剪接(alternative splicing)发生在前体m RNA向成熟m RNA的转换过程中,是转录后表达调控和产生蛋白质多样性的重要机制。可变剪接在真核生物中普遍存在,神经系统发育作为一个极其复杂且严密的过程,可变剪接对它的影响更明显。近年来,一些参与神经发育的可变剪接事件已经得到一定程度的验证,可以得知它的发生影响了突触生长、突触传递和神经干细胞的形成等生物学功能。同时,当可变剪接的模式发生改变时往往也会造成神经系统的功能异常。因此,本文就可变剪接的机制进行了简短的介绍,探索其在神经发育及神经疾病中的作用,并简单总结了相关数据库。  相似文献   

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基因选择性剪接的生物信息学研究概况   总被引:1,自引:1,他引:0  
林鲁萍  马飞  王义权 《遗传》2005,27(6):1001-1006
基因选择性剪接现象是真核生物基本而又重要的调控机制。由于基因的选择性剪接在形成生物复杂性和多样性上具有极其重要的作用,同时选择性剪接与许多人类疾病也密切相关。因此,研究基因选择性剪接是一项十分重要的工作。生物信息学作为一门新兴的学科在研究基因选择性剪接上起关键的作用,尤其在研究基因表达调控机制、选择性剪接基因预测以及选择性剪接基因进化上。本文综述了这方面的最新研究进展,为更深入了解真核生物基因的表达调控机理提供依据。  相似文献   

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mRNA的可变剪接是指一个单一的mRNA前体(pre-mRNA)经过不同的剪接加工方式生成多种mRNA变异体(variants)的过程,这些变异体最终可以编码合成具有不同结构和功能的蛋白质。在过去的10多年中,大量数据表明,可变剪接是增加转录组和蛋白质组多样性的重要资源,也是调控哺乳动物细胞基因表达的重要步骤。可变剪接具有高度的组织与发育阶段特异性,并受到外界信号的控制。剪接调控的紊乱与疾病的发生发展密切相关。该文将对哺乳动物细胞mRNA剪接调控的分子机制进行阐述。  相似文献   

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