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Immature large ribosomal subunits containing the 7S pre-rRNA can engage in translation in Saccharomyces cerevisiae

机译:含有7S pre-rRNA的未成熟大核糖体亚基可参与酿酒酵母的翻译

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摘要

Evolution has provided eukaryotes with mechanisms that impede immature and/or aberrant ribosomes to engage in translation. These mechanisms basically either prevent the nucleo-cytoplasmic export of these particles or, once in the cytoplasm, the release of associated assembly factors, which interfere with the binding of translation initiation factors and/or the ribosomal subunit joining. We have previously shown that aberrant yeast 40S ribosomal subunits containing the 20S pre-rRNA can engage in translation. In this study, we describe that cells harbouring the dob1-1 allele, encoding a mutated version of the exosome-assisting RNA helicase Mtr4, accumulate otherwise nuclear pre-60S ribosomal particles containing the 7S pre-rRNA in the cytoplasm. Polysome fractionation analyses revealed that these particles are competent for translation and do not induce elongation stalls. This phenomenon is rather specific since most mutations in other exosome components or co-factors, impairing the 3 end processing of the mature 5.8S rRNA, accumulate 7S pre-rRNAs in the nucleus. In addition, we confirm that pre-60S ribosomal particles containing either 5.8S + 30 or 5.8S + 5 pre-rRNAs also engage in translation elongation. We propose that 7S pre-rRNA processing is not strictly required for pre-60S r-particle export and that, upon arrival in the cytoplasm, there is no specific mechanism to prevent translation by premature pre-60S r-particles containing 3 extended forms of mature 5.8S rRNA.
机译:进化为真核生物提供了阻止未成熟和/或异常核糖体参与翻译的机制。这些机制基本上阻止了这些颗粒的核质输出,或者一旦进入细胞质,便释放了相关的装配因子,从而干扰了翻译起始因子和/或核糖体亚基的结合。先前我们已经表明,含有20S pre-rRNA的异常酵母40S核糖体亚基可以参与翻译。在这项研究中,我们描述了带有dob1-1等位基因的细胞,其编码外泌体辅助RNA解旋酶Mtr4的突变版本,否则会在细胞质中积累含有7S pre-rRNA的核60S核糖体颗粒。多核糖体分馏分析表明,这些颗粒具有翻译功能,不会引起延伸失速。这种现象相当特殊,因为其他外来体成分或辅因子中的大多数突变会损害成熟的5.8S rRNA的3末端加工,并在细胞核中积累7S pre-rRNA。此外,我们确认包含5.8S + 30或5.8S + 5 pre-rRNA的60S以前的核糖体颗粒也参与翻译延伸。我们建议7S pre-rRNA加工不是60S前r-粒子输出的严格要求,并且,到达细胞质后,没有特定的机制可防止含有3种扩展形式的60S r-粒子过早的翻译。成熟的5.8S rRNA。

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