U6及其拷贝在人类基因组调控中的潜力

M. Velázquez-Flores, R. R. Esparza-Garrido
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引用次数: 0

摘要

非编码RNA由大量具有难以想象的三维结构和功能的RNA分子组成。小核rna是剪接体机制的重要组成部分,它对mRNA的适当成熟至关重要。重要的是要补充的是,U6是形成剪接体的四种snrna之一,已被广泛研究。全长U6 (U6-1)基因座广泛分布在整个基因组中(200-900拷贝),但迄今为止已鉴定出少数U6全长基因座是潜在的活性基因。本文讨论了U6与其他snrna一起对退火靶序列的催化活性和识别的重要性,它在基因组中的进化以及基因组中有许多U6拷贝和假基因的事实,它与反转录转位的关联,以及它们在疾病中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential of U6 and Its Copies in the Regulation of the Human Genome
Non-coding RNAs are conformed by a large repertoire of RNA molecules with unimaginable tridimensional structures and functions. Small nuclear RNAs are an essential part of the spliceosome machinery, which is crucial for proper mRNA maturation. It is important to add that U6, one of the four snRNAs forming the spliceosome has been extensively studied. Full-length U6 (U6-1) loci are widely dispersed throughout the genome (200-900 copies), but a few U6 full-length loci have been identified to date as potentially active genes. The importance of U6 to carry out, together with other snRNAs, the catalytic activity and recognition of annealing target sequences, its evolution in the genome and the fact that the genome has many U6 copies and pseudogenes, its association with retrotransposition, as well as their implication in diseases is discussed in this review.
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