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线粒体DNA的缺失与……中DNA含量变异性的降低有关。

Loss of mitochondrial DNA is associated with reduced DNA content variability in .

作者信息

Putnam Christopher D

机构信息

Department of Medicine, University of California, San Diego, San Diego, California, United States.

出版信息

MicroPubl Biol. 2024 Mar 11;2024. doi: 10.17912/micropub.biology.001117. eCollection 2024.

DOI:10.17912/micropub.biology.001117
PMID:38533353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10964099/
Abstract

DNA content measurement by fluorescence-assisted cell sorting (FACS) provides information on cell cycle progression and DNA content variability. mutants with DNA content variability that was reduced relative to wild-type strains had defects in mitochondrial DNA (mtDNA) maintenance and mitochondrial gene expression and were correlated with strains found to lack mtDNA ([ ] cells) by genome sequencing and fluorescence microscopy. In contrast, mutants with increased variability had defects in cell cycle progression, which may indicate a loss of coordination between mtDNA and nuclear DNA replication. Thus, FACS measurement of DNA content variability can provide insight into cell-to-cell heterogeneity in mtDNA copy number.

摘要

通过荧光辅助细胞分选(FACS)测量DNA含量可提供有关细胞周期进程和DNA含量变异性的信息。与野生型菌株相比,DNA含量变异性降低的突变体在线粒体DNA(mtDNA)维持和线粒体基因表达方面存在缺陷,并且与通过基因组测序和荧光显微镜检查发现缺乏mtDNA的菌株([ ]细胞)相关。相比之下,变异性增加的突变体在细胞周期进程方面存在缺陷,这可能表明mtDNA与核DNA复制之间失去了协调性。因此,对DNA含量变异性进行FACS测量可以深入了解mtDNA拷贝数的细胞间异质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d9b/10964099/3c4be3b30649/25789430-2024-micropub.biology.001117.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d9b/10964099/3c4be3b30649/25789430-2024-micropub.biology.001117.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d9b/10964099/3c4be3b30649/25789430-2024-micropub.biology.001117.jpg

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本文引用的文献

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The metabolic growth limitations of petite cells lacking the mitochondrial genome.缺乏线粒体基因组的 petite 细胞的代谢生长限制。
Nat Metab. 2021 Nov;3(11):1521-1535. doi: 10.1038/s42255-021-00477-6. Epub 2021 Nov 18.
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Systematic analysis of nuclear gene function in respiratory growth and expression of the mitochondrial genome in .
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