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5'剪接位点:系统发育进化及与U1RNA结合的可变几何结构

The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.

作者信息

Jacob M, Gallinaro H

机构信息

Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Strasbourg, France.

出版信息

Nucleic Acids Res. 1989 Mar 25;17(6):2159-80. doi: 10.1093/nar/17.6.2159.

Abstract

The 5' splice site sequences of 3294 introns from various organisms (1-672) were analyzed in order to determine the rules governing evolution of this sequence, which may shed light on the mechanism of cleavage at the exon-intron junction. The data indicate that, currently, in all organisms, a common sequence 1GUAAG6U and its derivatives are used as well as an additional sequence and its derivatives, which differ in metazoa (G/1GUgAG6U), lower eucaryotes (1GUAxG6U) and higher plants (AG/1GU3A). They all partly resemble the prototype sequence AG/1GUAAG6U whose 8 contigous nucleotides are complementary to the nucleotides 4-11 of U1RNA, which are perfectly conserved in the course of phylogenetic evolution. Detailed examination of the data shows that U1RNA can recognize different parts of 5' splice sites. As a rule, either prototype nucleotides at position -2 and -1 or at positions 4, 5 or 6 or at positions 3-4 are dispensable provided that the stability of the U1RNA-5' splice site hybrid is conserved. On the basis of frequency of sequences, the optimal size of the hybridizable region is 5-7 nucleotides. Thus, the cleavage at the exon-intron junction seems to imply, first, that the 5' splice site is recognized by U1RNA according to a "variable geometry" program; second, that the precise cleavage site is determined by the conserved sequence of U1RNA since it occurs exactly opposite to the junction between nucleotides C9 and C10 of U1RNA. The variable geometry of the U1RNA-5' splice site association provides flexibility to the system and allows diversification in the course of phylogenetic evolution.

摘要

为了确定该序列的进化规则,从而揭示外显子-内含子连接处的切割机制,我们分析了来自各种生物体(1 - 672)的3294个内含子的5'剪接位点序列。数据表明,目前在所有生物体中,通用序列1GUAAG6U及其衍生物以及另一种序列及其衍生物都被使用,后一种序列在后生动物(G/1GUgAG6U)、低等真核生物(1GUAxG6U)和高等植物(AG/1GU3A)中有所不同。它们都部分类似于原型序列AG/1GUAAG6U,其8个连续核苷酸与U1RNA的核苷酸4 - 11互补,这些核苷酸在系统发育进化过程中是完全保守的。对数据的详细检查表明,U1RNA可以识别5'剪接位点的不同部分。通常,只要U1RNA - 5'剪接位点杂交体的稳定性得以保持,-2和-1位、4、5或6位或3 - 4位的原型核苷酸是可有可无的。根据序列频率,可杂交区域的最佳大小为5 - 7个核苷酸。因此,外显子-内含子连接处的切割似乎意味着,首先,5'剪接位点由U1RNA根据“可变几何结构”程序识别;其次,精确的切割位点由U1RNA的保守序列决定,因为它恰好发生在U1RNA的核苷酸C9和C10之间的连接处相对的位置。U1RNA - 5'剪接位点结合的可变几何结构为该系统提供了灵活性,并允许在系统发育进化过程中发生多样化。

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