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Pseudoknot in the central domain of small subunit ribosomal RNA is essential for translation.

机译:小亚基核糖体RNA中央结构域中的假结对于翻译至关重要。

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摘要

Phylogenetic comparison of rRNA sequences has suggested that a pseudoknot structure exists in the central domain of small-subunit rRNA. In Escherichia coli 16S rRNA, this pseudoknot would form when positions 570 and 571 pair with positions 865 and 866. Mutations were introduced into this pseudoknot at the phylogenetically invariant nucleotides U571 and A865. Single mutations of U to A at 571 or A to U at 865 dramatically altered the structural stability of the 30S subunit and also impaired the function of the subunit in translation. When the mutations were combined to create a compensatory pairing, the normal structure of the 30S subunit was restored, and the function of the mutant subunit in translation returned to wild-type levels. These results demonstrate the existence of a higher order structure in rRNA that directly affects the folding of the 30S subunit. Given the position of this structure in the three-dimensional model of the small subunit and the additional interactions that are likely to form in the same rRNA region, the central domain pseudoknot appears to contribute to a complex structure of rRNA that controls the conformational state of the ribosome.
机译:rRNA序列的系统发生比较表明,小亚基rRNA的中央结构域中存在假结结构。在大肠杆菌16S rRNA中,当第570位和第571位与第865位和第866位配对时会形成该假结。在系统发育不变的核苷酸U571和A865处将突变引入到该假结中。 U在571突变为A或865在A突变为U极大地改变了30S亚基的结构稳定性,并削弱了该亚基在翻译中的功能。当将突变组合以产生补偿配对时,恢复了30S亚基的正常结构,并且突变亚基在翻译中的功能恢复到野生型水平。这些结果表明,在rRNA中存在直接影响30S亚基折叠的更高阶结构。鉴于此结构在小亚基的三维模型中的位置以及可能在同一rRNA区域中形成的其他相互作用,中央结构域假结似乎有助于控制rRNA构象状态的rRNA复杂结构。核糖体。

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