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首页> 外文期刊>Cell biology international. >Mitosis is not the only distributor of mutated cells: non-mitotic endopolyploid cells produce reproductive genome-reduced cells.
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Mitosis is not the only distributor of mutated cells: non-mitotic endopolyploid cells produce reproductive genome-reduced cells.

机译:有丝分裂不是突变细胞的唯一分配者:非有丝分裂内源多倍体细胞产生生殖基因组减少的细胞。

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Giant endopolyploid nuclei (>16n) can spontaneously fragment by endomitosis (nuclear internal division) into near-diploid cells with reproductive capacity (depolyploidization), and endotetra/octopolyploidy can undergo chromosome-visible meiotic-like genome reductional divisions also to replicative subcells. These unconventional divisions are associated with production of aneuploidy, which led to the question in this study of whether endopolyploidy, in general, can contribute genetic variability to tumorigenic potential. For this purpose, non-proliferative endopolyploid cells (range: 4n-32n) in near-senescence of normal diploid cell strains were analysed for nuclear-morphogenic changes associated with the presence of diploid-sized nuclei in the cytoplasm. A one-by-one nuclear-cutoff process gave rise to reproducing genome-reduced cells. It was concluded that these unconventional cell divisions are, indeed, suspects of originating genetic variability. Details of these irregular mitoses were compared to 'mitotic-meiosis' in primitive organisms, which suggested activation of an ancestral trait in the mammalian cells.
机译:巨大的内倍体核(> 16n)可以通过内吞作用(核内分裂)自发分裂成具有繁殖能力的近二倍体细胞(去多倍体化),而内四倍体/八倍体可以经历染色体可见的减数分裂样基因组还原分裂,也可以复制到复制性亚细胞上。这些非常规的分裂与非整倍性的产生有关,这导致了本研究中的一个问题,即多倍体通常是否可以导致致癌潜力的遗传变异。为此目的,分析了正常二倍体细胞株接近衰老的非增殖性内源多倍体细胞(范围:4n-32n)中与细胞质中二倍体大小的核有关的核形态发生变化。一对一的核切除过程产生了繁殖减少基因组的细胞。结论是,这些非常规的细胞分裂确实是起源遗传变异的怀疑。将这些不规则有丝分裂的细节与原始生物体中的“有丝分裂减数分裂”进行了比较,这提示了哺乳动物细胞中祖先性状的激活。

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