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真核生物5S核糖体RNA中碱基替换的定量分析:对RNA二级结构维持的选择

Quantitation of base substitutions in eukaryotic 5S rRNA: selection for the maintenance of RNA secondary structure.

作者信息

Curtiss W C, Vournakis J N

出版信息

J Mol Evol. 1984;20(3-4):351-61. doi: 10.1007/BF02104741.

DOI:10.1007/BF02104741
PMID:6439889
Abstract

Eukaryotic 5S rRNA sequences from 34 diverse species were compared by the following method: (1) The sequences were aligned; (2) the positions of substitutions were located by comparison of all possible pairs of sequences; (3) the substitution sites were mapped to an assumed general base pairing model; and (4) the R-Y model of base stacking was used to study stacking pattern relationships in the structure. An analysis of the sequence and structure variability in each region of the molecule is presented. It was found that the degree of base substitution varies over a wide range, from absolute conservation to occurrence of over 90% of the possible observable substitutions. The substitutions are located primarily in stem regions of the 5S rRNA secondary structure. More than 88% of the substitutions in helical regions maintain base pairing. The disruptive substitutions are primarily located at the edges of helical regions, resulting in shortening of the helical regions and lengthening of the adjacent nonpaired regions. Base stacking patterns determined by the R-Y model are mapped onto the general secondary structure. Intrastrand and interstrand stacking could stabilize alternative coaxial structures and limit the conformational flexibility of nonpaired regions. Two short contiguous regions are 100% conserved in all species. This may reflect evolutionary constraints imposed at the DNA level by the requirement for binding of a 5S gene transcription initiation factor during gene expression.

摘要

采用以下方法对来自34个不同物种的真核生物5S rRNA序列进行了比较:(1) 对序列进行比对;(2) 通过比较所有可能的序列对来确定替换位点;(3) 将替换位点映射到假定的通用碱基配对模型上;(4) 使用碱基堆积的R-Y模型来研究结构中的堆积模式关系。本文对分子每个区域的序列和结构变异性进行了分析。结果发现,碱基替换程度在很大范围内变化,从绝对保守到出现超过90%的可能可观察到的替换。替换主要位于5S rRNA二级结构的茎区。螺旋区域中超过88%的替换保持碱基配对。破坏性替换主要位于螺旋区域的边缘,导致螺旋区域缩短和相邻非配对区域延长。由R-Y模型确定的碱基堆积模式被映射到通用二级结构上。链内和链间堆积可以稳定替代的同轴结构,并限制非配对区域的构象灵活性。两个短的连续区域在所有物种中100%保守。这可能反映了基因表达过程中5S基因转录起始因子结合需求在DNA水平上施加的进化限制。

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本文引用的文献

1
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences.一种通过核苷酸序列比较研究来估计碱基替换进化速率的简单方法。
J Mol Evol. 1980 Dec;16(2):111-20. doi: 10.1007/BF01731581.
2
The ternary complex consisting of rat liver ribosomal 5 S RNA, 5.8 S RNA and protein L5.由大鼠肝脏核糖体5 S RNA、5.8 S RNA和蛋白质L5组成的三元复合物。
FEBS Lett. 1980 Sep 22;119(1):81-4. doi: 10.1016/0014-5793(80)81002-7.
3
A control region in the center of the 5S RNA gene directs specific initiation of transcription: II. The 3' border of the region.
通过对核苷酸碱基变化在突变和选择方面的全面分析推断出的陆地植物的深层系统发育。
J Mol Evol. 2004 Apr;58(4):479-89. doi: 10.1007/s00239-003-2570-y.
4
Chemical and computer probing of RNA structure.RNA结构的化学与计算机探测
Prog Nucleic Acid Res Mol Biol. 1996;53:131-96. doi: 10.1016/s0079-6603(08)60144-0.
5
Secondary structure of Tetrahymena thermophilia 5S ribosomal RNA as revealed by enzymatic digestion and microdensitometric analysis.嗜热四膜虫5S核糖体RNA二级结构的酶切消化与显微光密度分析揭示
Nucleic Acids Res. 1986 Feb 11;14(3):1365-78. doi: 10.1093/nar/14.3.1365.
5S RNA基因中心的一个控制区域指导转录的特异性起始:II. 该区域的3'边界。
Cell. 1980 Jan;19(1):27-35. doi: 10.1016/0092-8674(80)90385-2.
4
A control region in the center of the 5S RNA gene directs specific initiation of transcription: I. The 5' border of the region.5S RNA基因中心的一个控制区域指导转录的特异性起始:I. 该区域的5'边界。
Cell. 1980 Jan;19(1):13-25. doi: 10.1016/0092-8674(80)90384-0.
5
The binding of a transcription factor to deletion mutants of a 5S ribosomal RNA gene.转录因子与5S核糖体RNA基因缺失突变体的结合。
Cell. 1981 Mar;23(3):665-9. doi: 10.1016/0092-8674(81)90429-3.
6
Computer comparison of new and existing criteria for constructing evolutionary trees from sequence data.从序列数据构建进化树的新的和现有标准的计算机比较。
J Mol Evol. 1982;19(1):9-19. doi: 10.1007/BF02100219.
7
Generalized structures of the 5S ribosomal RNAs.5S核糖体RNA的通用结构
Nucleic Acids Res. 1982 Nov 25;10(22):7323-44. doi: 10.1093/nar/10.22.7323.
8
Comparative sequence analysis as an approach to evaluating structure, function, and evolution of 5S and 5.8S ribosomal RNAs.比较序列分析作为评估5S和5.8S核糖体RNA的结构、功能及进化的一种方法。
Can J Biochem. 1982 Apr;60(4):480-9. doi: 10.1139/o82-057.
9
Adenine-guanine base pairing ribosomal RNA.腺嘌呤 - 鸟嘌呤碱基配对核糖体RNA
Nucleic Acids Res. 1982 Apr 24;10(8):2701-8. doi: 10.1093/nar/10.8.2701.
10
The evolving tRNA molecule.不断进化的转运RNA分子。
CRC Crit Rev Biochem. 1981;11(1):35-104. doi: 10.3109/10409238109108699.