首页> 美国卫生研究院文献>Nucleic Acids Research >Selective isolation and detailed analysis of intra-RNA cross-links induced in the large ribosomal subunit of E. coli: a model for the tertiary structure of the tRNA binding domain in 23S RNA.
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Selective isolation and detailed analysis of intra-RNA cross-links induced in the large ribosomal subunit of E. coli: a model for the tertiary structure of the tRNA binding domain in 23S RNA.

机译:在大肠杆菌大核糖体亚基中诱导的RNA内交联的选择性分离和详细分析:23S RNA中tRNA结合域的三级结构模型。

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摘要

Intramolecular RNA cross-links were induced within the large ribosomal subunit of E. coli by mild ultraviolet irradiation. Regions of the 23S RNA previously implicated in interactions with ribosomal-bound tRNA were then specifically excised by addressed cleavage using ribonuclease H, in conjunction with synthetic complementary decadeoxyribonucleotides. Individual cross-linked fragments within these regions released by such 'directed digests' were isolated by two-dimensional gel electrophoresis and the sites involved in the cross-links determined using classical oligonucleotide analysis techniques. Using this approach, seven 'new' cross-links could be precisely localised, between positions 1782 and 2608-2609, 1940 and 2554, 1941-1942 and 1964-1965, 1955 and 2552-2553, 2145-2146 and 2202, 2518-2519 and 2544-2545, and between positions 2790-2791 and 2892-2895 in the 23S RNA sequence. These data, in conjunction with data from RNA-protein cross-linking studies carried out in our laboratory, were used to define a model for the tertiary organisation of the tRNA binding domain of 23S RNA 'in situ', in which the specific nucleotides associated with tRNA binding in the 'A' and 'P' sites are clustered at the base of the 'central protuberance' of the 50S subunit.
机译:通过温和的紫外线照射,在大肠杆菌的大核糖体亚基内诱导了分子内RNA交联。然后,通过使用核糖核酸酶H结合合成互补的十氧杂核糖核苷酸,通过有针对性的切割来特异性切除先前牵涉与核糖体结合的tRNA相互作用的23S RNA区域。通过二维凝胶电泳分离由这些“定向消化”释放的这些区域内的各个交联片段,并使用经典的寡核苷酸分析技术确定参与交联的位点。使用这种方法,可以在位置1782和2608-2609、1940和2554、1941-1942和1964-1965、1955和2552-2553、2145-2146和2202、2518- 2519和2544-2545,以及在23S RNA序列中的2790-2791和2892-2895之间。这些数据与在我们实验室中进行的RNA-蛋白质交联研究的数据一起,用于定义“原位” 23S RNA的tRNA结合域的三级组织模型,其中特定的核苷酸相关在“ A”和“ P”位点具有tRNA结合的分子聚集在50S亚基的“中央突起”基部。

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