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探究16S核糖体RNA 3'主要结构域的组装。涉及核糖体蛋白S7、S9和S19的四级相互作用。

Probing the assembly of the 3' major domain of 16 S ribosomal RNA. Quaternary interactions involving ribosomal proteins S7, S9 and S19.

作者信息

Powers T, Changchien L M, Craven G R, Noller H F

机构信息

Thimann Laboratories, University of California, Santa Cruz 95064.

出版信息

J Mol Biol. 1988 Mar 20;200(2):309-19. doi: 10.1016/0022-2836(88)90243-4.

Abstract

We have studied the effect of assembly of ribosomal proteins S7, S9 and S19 on the accessibility and conformation of nucleotides in 16 S ribosomal RNA. Complexes formed between 16 S rRNA and S7, S7 + S9, S7 + S19 or S7 + S9 + S19 were subjected to a combination of chemical and enzymatic probes, whose sites of attack in 16 S rRNA were identified by primer extension. The results of this study show that: (1) Protein S7 affects the reactivity of an extensive region in the lower half of the 3' major domain. Inclusion of proteins S9 or S19 with S7 has generally little additional effect on S7-specific protection of the RNA. Clusters of nucleotides that are protected by protein S7 are localized in the 935-945 region, the 950/1230 stem, the 1250/1285 internal loop, and the 1350/1370 stem. (2) Addition of protein S9 in the presence of S7 causes several additional effects principally in two structurally distal regions. We observe strong S9-dependent protection of positions 1278 to 1283, and of several positions in the 1125/1145 internal loop. These findings suggest that interaction of protein S9 with 16 S rRNA results in a structure in which the 1125/1145 and 1280 regions are proximal to each other. (3) Most of the strong S19-dependent effects are clustered in the 950-1050 and 1210-1230 regions, which are joined by base-pairing in the 16 S rRNA secondary structure. The highly conserved 960-975 stemp-loop, which has been implicated in tRNA binding, appears to be destabilized in the presence of S19. (4) Protein S7 causes enhanced reactivity at several sites that become protected upon addition of S9 or S19. This suggests that S7-induced conformational changes in 16 S rRNA play a role in the co-operativity of assembly of the 3' major domain.

摘要

我们研究了核糖体蛋白S7、S9和S19的组装对16S核糖体RNA中核苷酸可及性和构象的影响。使16S rRNA与S7、S7 + S9、S7 + S19或S7 + S9 + S19形成的复合物接受化学和酶促探针的联合作用,通过引物延伸确定这些探针在16S rRNA中的攻击位点。本研究结果表明:(1)蛋白S7影响3' 主要结构域下半部分一个广泛区域的反应性。将蛋白S9或S19与S7一起加入,通常对RNA的S7特异性保护几乎没有额外影响。受蛋白S7保护的核苷酸簇位于935 - 945区域、950/1230茎、1250/1285内环和1350/1370茎中。(2)在S7存在的情况下加入蛋白S9会产生一些额外的影响,主要在两个结构上较远的区域。我们观察到对1278至1283位以及1125/1145内环中的几个位点有强烈的S9依赖性保护。这些发现表明蛋白S9与16S rRNA的相互作用导致一种结构,其中1125/1145和1280区域彼此靠近。(3)大多数强烈的S19依赖性影响集中在950 - 1050和1210 - 1230区域,它们在16S rRNA二级结构中通过碱基配对相连。高度保守的960 - 975茎环,与tRNA结合有关,在S19存在时似乎不稳定。(4)蛋白S7在加入S9或S19后受保护的几个位点处导致反应性增强。这表明S7诱导的16S rRNA构象变化在3' 主要结构域的组装协同性中起作用。

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