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首页> 外文期刊>Nucleic acids research >The dhp1+ gene, encoding a putative nuclear 5′→3′ exoribonuclease, is required for proper chromosome segregation in fission yeast
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The dhp1+ gene, encoding a putative nuclear 5′→3′ exoribonuclease, is required for proper chromosome segregation in fission yeast

机译:dhp1 +基因编码假定的5'→3'核外切核酸外切酶,是裂变酵母中正确染色体分离所必需的

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摘要

The Schizosaccharomyces pombe dhp1+ gene is an ortholog of the Saccharomyces cerevisiae RAT1 gene, which encodes a nuclear 5′→3′ exoribonuclease, and is essential for cell viability. To clarify the cellular functions of the nuclear 5′→3′ exoribonuclease, we isolated and characterized a temperature-sensitive mutant of dhp1 (dhp1-1 mutant). The dhp1-1 mutant showed nuclear accumulation of poly(A)+ RNA at the restrictive temperature, as was already reported for the rat1 mutant. Interestingly, the dhp1-1 mutant exhibited aberrant chromosome segregation at the restrictive temperature. The dhp1-1 cells frequently contained condensed chromosomes, most of whose sister chromatids failed to separate during mitosis despite normal mitotic spindle elongation. Finally, chromosomes were displaced or unequally segregated. As similar mitotic defects were also observed in Dhp1p-depleted cells, we concluded that dhp1+ is required for proper chromosome segregation as well as for poly(A)+ RNA metabolism in fission yeast. Furthermore, we isolated a multicopy suppressor of the dhp1-1 mutant, referred to as din1+. We found that the gene product of dhp1-1 was unstable at high temperatures, but that reduced levels of Dhp1-1p could be suppressed by overexpressing Din1p at the restrictive temperature. Thus, Din1p may physically interact with Dhp1p and stabilize Dhp1p and/or restore its activity.
机译:粟酒裂殖酵母dhp1 + 基因是酿酒酵母RAT1基因的直系同源基因,它编码5'→3'核外切核糖核酸酶,对细胞活力至关重要。为了阐明核5'→3'核糖核酸外切酶的细胞功能,我们分离并鉴定了dhp1的温度敏感突变体(dhp1-1突变体)。 dhp1-1突变体在限制性温度下显示了poly(A)supRNA + sup> RNA的核积累,正如rat1突变体已经报道的那样。有趣的是,dhp1-1突变体在限制性温度下表现出异常的染色体分离。 dhp1-1细胞通常含有浓缩染色体,尽管有丝分裂纺锤体正常伸长,但大多数有色染色体姊妹染色单体均无法分离。最后,染色体被置换或分离不均。由于在耗尽Dhp1p的细胞中也观察到类似的有丝分裂缺陷,因此我们得出结论,dhp1 + 是正常染色体分离以及poly(A) + RNA代谢所必需的。裂变酵母。此外,我们分离了dhp1-1突变体的多拷贝抑制子,称为din1 + 。我们发现dhp1-1的基因产物在高温下不稳定,但是在限制性温度下过表达Din1p可以抑制Dhp1-1p的降低水平。因此,Din1p可能与Dhp1p发生物理相互作用并稳定Dhp1p和/或恢复其活性。

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