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DNA breaks and chromosome pulverization from errors in mitosis

机译:由于有丝分裂的错误,DNA断裂和染色体粉碎

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摘要

The involvement of whole-chromosome aneuploidy in tumorigenesis is the subject of debate, in large part because of the lack of insight into underlying mechanisms. Here we identify a mechanism by which errors in mitotic chromosome segregation generate DNA breaks via the formation of structures called micronuclei. Whole-chromosome-containing micronuclei form when mitotic errors produce lagging chromosomes. We tracked the fate of newly generated micronuclei and found that they undergo defective and asynchronous DNA replication, resulting in DNA damage and often extensive fragmentation of the chromosome in the micronucleus. Micronuclei can persist in cells over several generations but the chromosome in the micronucleus can also be distributed to daughter nuclei. Thus, chromosome segregation errors potentially lead to mutations and chromosome rearrangements that can integrate into the genome. Pulverization of chromosomes in micronuclei may also be one explanation for 'chromothripsis' in cancer and developmental disorders, where isolated chromosomes or chromosome arms undergo massive local DNA breakage and rearrangement.
机译:全染色体非整倍性在肿瘤发生中的参与是争论的主题,很大程度上是由于缺乏对潜在机制的了解。在这里,我们确定一种机制,通过该机制,有丝分裂染色体分离中的错误通过称为微核的结构的形成而产生DNA断裂。当有丝分裂错误产生滞后染色体时,会形成含全染色体的微核。我们追踪了新产生的微核的命运,发现它们经历了有缺陷的异步DNA复制,从而导致DNA损伤,并且经常使微核中的染色体发生广泛的断裂。微核可以在细胞中保留数代,但微核中的染色体也可以分布到子核。因此,染色体分离错误可能会导致突变和染色体重排,从而整合到基因组中。微核中的染色体粉化也可能是癌症和发育障碍中“染色体上皮病”的一种解释,其中分离的染色体或染色体臂会发生局部局部DNA断裂和重排。

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  • 来源
    《Nature》 |2012年第7383期|p.53-58|共6页
  • 作者单位

    Department of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, Massachusetts 02115, USA Howard Hughes Medical Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA. 4Belfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute, 4 Blackfan Street, Boston, Massachusetts 02115, USA;

    Department of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, Massachusetts 02115, USA Howard Hughes Medical Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA. 4Belfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute, 4 Blackfan Street, Boston, Massachusetts 02115, USA;

    Department of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, Massachusetts 02115, USA Howard Hughes Medical Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA. 4Belfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute, 4 Blackfan Street, Boston, Massachusetts 02115, USA;

    Department of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA;

    Belfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute, 4 Blackfan Street, Boston, Massachusetts 02115, USA;

    Department of Radiation Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA;

    Department of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA;

    Belfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute, 4 Blackfan Street, Boston, Massachusetts 02115, USA;

    Department of Radiation Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA;

    Department of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, Massachusetts 02115, USA Howard Hughes Medical Institute, 450 Brookline Avenue, Boston, Massachusetts 02115, USA;

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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:54:01

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