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酿酒酵母二倍体特异性[校正]基因组稳定基因:全基因组筛选揭示了通过单倍体化逃避持续的 DNA 重排应激。

Diploid-specific [corrected] genome stability genes of S. cerevisiae: genomic screen reveals haploidization as an escape from persisting DNA rearrangement stress.

机构信息

Laboratory of Mutagenesis and DNA Repair, Institute of Biochemistry and Biophysics, Polish Academy of Science, Warsaw, Poland.

出版信息

PLoS One. 2011;6(6):e21124. doi: 10.1371/journal.pone.0021124. Epub 2011 Jun 17.

Abstract

Maintaining a stable genome is one of the most important tasks of every living cell and the mechanisms ensuring it are similar in all of them. The events leading to changes in DNA sequence (mutations) in diploid cells occur one to two orders of magnitude more frequently than in haploid cells. The majority of those events lead to loss of heterozygosity at the mutagenesis marker, thus diploid-specific genome stability mechanisms can be anticipated. In a new global screen for spontaneous loss of function at heterozygous forward mutagenesis marker locus, employing three different mutagenesis markers, we selected genes whose deletion causes genetic instability in diploid Saccharomyces cerevisiae cells. We have found numerous genes connected with DNA replication and repair, remodeling of chromatin, cell cycle control, stress response, and in particular the structural maintenance of chromosome complexes. We have also identified 59 uncharacterized or dubious ORFs, which show the genome instability phenotype when deleted. For one of the strongest mutators revealed in our screen, ctf18Δ/ctf18Δ the genome instability manifests as a tendency to lose the whole set of chromosomes. We postulate that this phenomenon might diminish the devastating effects of DNA rearrangements, thereby increasing the cell's chances of surviving stressful conditions. We believe that numerous new genes implicated in genome maintenance, together with newly discovered phenomenon of ploidy reduction, will help revealing novel molecular processes involved in the genome stability of diploid cells. They also provide the clues in the quest for new therapeutic targets to cure human genome instability-related diseases.

摘要

维持稳定的基因组是每个活细胞最重要的任务之一,确保这一任务的机制在所有细胞中都相似。在二倍体细胞中,导致 DNA 序列改变(突变)的事件发生的频率比在单倍体细胞中高一到两个数量级。这些事件中的大多数导致诱变标记处的杂合性丢失,因此可以预期二倍体特有的基因组稳定性机制。在一项新的针对自发功能丧失的全球筛选中,我们使用了三个不同的诱变标记,在异源正向诱变标记基因座中筛选出导致二倍体酿酒酵母细胞遗传不稳定性的基因。我们发现了许多与 DNA 复制和修复、染色质重塑、细胞周期控制、应激反应有关的基因,特别是与染色体复合物的结构维持有关的基因。我们还鉴定了 59 个未表征或可疑的 ORF,当这些基因缺失时,会表现出基因组不稳定表型。在我们的筛选中发现的一个最强的诱变剂 ctf18Δ/ctf18Δ,其基因组不稳定表现为失去整套染色体的趋势。我们假设这种现象可能会减轻 DNA 重排的破坏性影响,从而增加细胞在应激条件下生存的机会。我们相信,许多与基因组维护相关的新基因,以及新发现的倍性降低现象,将有助于揭示涉及二倍体细胞基因组稳定性的新分子过程。它们还为寻找治疗人类基因组不稳定性相关疾病的新治疗靶点提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8614/3117874/015a520374a6/pone.0021124.g001.jpg

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