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维持M1双链RNA病毒所必需的Mak5p由酵母开放阅读框YBR142w编码,并参与核糖体60S亚基的生物合成。

Mak5p, which is required for the maintenance of the M1 dsRNA virus, is encoded by the yeast ORF YBR142w and is involved in the biogenesis of the 60S subunit of the ribosome.

作者信息

Zagulski M, Kressler D, Bécam A-M, Rytka J, Herbert C J

机构信息

Institute of Biochemistry and Biophysics, Polish National Academy of Sciences, 5a Pawinskiego, 02-106 Warsaw, Poland.

出版信息

Mol Genet Genomics. 2003 Nov;270(3):216-24. doi: 10.1007/s00438-003-0913-4. Epub 2003 Sep 9.

Abstract

In this study, we show that the Saccharomyces cerevisiae ORF YBR142w, which encodes a putative DEAD-box RNA helicase, corresponds to MAK5. The mak5-1 allele is deficient in the maintenance of the M1 dsRNA virus, resulting in a killer minus phenotype. This allele carries two mutations, G218D in the conserved ATPase A-motif and P618S in a non-conserved region. We have separated these mutations and shown that it is the G218D mutation that is responsible for the killer minus phenotype. Mak5p is an essential nucleolar protein; depletion of the protein leads to a reduction in the level of 60S ribosomal subunits, the appearance of half-mer polysomes, and a delay in production of the mature 25S and 5.8S rRNAs. Thus, Mak5p is involved in the biogenesis of 60S ribosomal subunits.

摘要

在本研究中,我们发现酿酒酵母开放阅读框YBR142w编码一种假定的DEAD-box RNA解旋酶,它对应于MAK5。mak5-1等位基因在维持M1双链RNA病毒方面存在缺陷,导致杀伤性阴性表型。该等位基因携带两个突变,保守ATP酶A基序中的G218D和非保守区域中的P618S。我们分离了这些突变,并表明是G218D突变导致了杀伤性阴性表型。Mak5p是一种必需的核仁蛋白;该蛋白的缺失会导致60S核糖体亚基水平降低、半聚核糖体出现以及成熟25S和5.8S rRNA产生延迟。因此,Mak5p参与60S核糖体亚基的生物合成。

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