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The 5' end of the 18S rRNA can be positioned from within the mature rRNA.

机译:18S rRNA的5'末端可位于成熟rRNA内。

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摘要

In yeast, the 5' end of the mature 18S rRNA is generated by endonucleolytic cleavage at site A1, the position of which is specified by two distinct signals. An evolutionarily conserved sequence immediately upstream of the cleavage site has previously been shown to constitute one of these signals. We report here that a conserved stem-loop structure within the 5' region of the 18S rRNA is recognized as a second positioning signal. Mutations predicted to either extend or destabilize the stem inhibited the normal positioning of site A1 from within the 18S rRNA sequence, as did substitution of the loop nucleotides. In addition, these mutations destabilized the mature 18S rRNA, indicating that recognition of the stem-loop structure is also required for 18S rRNA stability. Several mutations tested reduced the efficiency of pre-rRNA cleavage at site A1. There was, however, a poor correlation between the effects of the different mutations on the efficiency of cleavage and on the choice of cleavage site, indicating that these involve recognition of the stem-loop region by distinct factors. In contrast, the cleavages at sites A1 and A2 are coupled and the positioning signals appear to be similar, suggesting that both cleavages may be carried out by the same endonuclease.
机译:在酵母中,成熟的18S rRNA的5'端通过位点A1的内切核酸酶切产生,其位置由两个不同的信号指定。先前已显示出切割位点上游的进化保守序列构成了这些信号之一。我们在这里报告在18S rRNA的5'区域内的保守茎环结构被认为是第二个定位信号。预测会延长或破坏茎干的突变会抑制18S rRNA序列中位点A1的正常定位,就像环核苷酸的取代一样。另外,这些突变使成熟的18S rRNA不稳定,表明18S rRNA稳定性也需要识别茎环结构。测试的几个突变降低了位点A1上rRNA裂解的效率。但是,不同突变对切割效率和切割位点选择的影响之间存在很弱的相关性,表明这些突变涉及通过不同因素识别茎环区域。相反,位点A1和A2处的切割是偶联的,并且定位信号看起来是相似的,这表明两个切割可以由相同的核酸内切酶进行。

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