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Structural and functional analysis of Escherichia coli ribosomes containing small deletions around position 1760 in the 23S ribosomal RNA.

机译:大肠杆菌核糖体的结构和功能分析,该核糖体在23S核糖体RNA中位于1760位附近有少量缺失。

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摘要

Three different small deletions were produced at a single Pvu 2 restriction site in E. coli 23S rDNA of plasmid pKK 3535 using exonuclease Bal 31. The deletions were located around position 1760 in 23S rRNA and were characterized by DNA sequencing as well as by direct fingerprinting and S1-mapping of the rRNA. Two of the mutant plasmids, Pvu 2-32 and Pvu 2-33, greatly reduced the growth rate of transformed cells while the third mutant, Pvu 2-14 grew as fast as cells containing the wild-type plasmid pKK 3535. All three mutant 23S rRNAs were incorporated into 50S-like particles and were even found in 70S ribosomes and polysomes in vivo. The conformation of mutant 23S rRNA in 50S subunits was probed with a double-strand specific RNase from cobra venom. These analyses revealed changes in the accessibility of cleavage sites near the deletions around position 1760 and in the area around position 800 in all three mutant rRNAs. We suggest, that an altered conformation of the rRNAs at the site of the deletion is responsible for the slow growth of cells containing mutant plasmids Pvu 2-32 and Pvu 2-33.
机译:使用核酸外切酶Bal 31在质粒pKK 3535的大肠杆菌23S rDNA的单个Pvu 2限制性酶切位点处产生三个不同的小缺失。该缺失位于23S rRNA中的1760位附近,并通过DNA测序和直接指纹鉴定来表征rRNA的S1映射。两个突变质粒Pvu 2-32和Pvu 2-33大大降低了转化细胞的生长速度,而第三个突变质粒Pvu 2-14的生长速度与包含野生型质粒pKK 3535的细胞一样快。所有三个突变体将23S rRNA掺入50S样颗粒中,甚至在体内发现于70S核糖体和多核糖体中。用来自眼镜蛇毒的双链特异性RNA酶探测50S亚基中的突变23S rRNA的构象。这些分析揭示了在所有三个突变rRNA中,在位置1760附近的缺失附近和在位置800附近的区域中切割位点的可及性的变化。我们建议,在缺失位点的rRNA的构象改变是造成含有突变质粒Pvu 2-32和Pvu 2-33的细胞缓慢生长的原因。

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  • 作者

    Zweib, C; Dahlberg, A E;

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  • 年度 1984
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  • 原文格式 PDF
  • 正文语种 en
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