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哺乳动物中癌症易感性的跨代表观遗传遗传。

Intergenerational epigenetic inheritance of cancer susceptibility in mammals.

机构信息

Whitehead Institute, Cambridge, United States.

Department of Medicine, Division of Hematology, Brigham and Women's Hospital, Harvard Medical School, Boston, United States.

出版信息

Elife. 2019 Apr 9;8:e39380. doi: 10.7554/eLife.39380.

Abstract

Susceptibility to cancer is heritable, but much of this heritability remains unexplained. Some 'missing' heritability may be mediated by epigenetic changes in the parental germ line that do not involve transmission of genetic variants from parent to offspring. We report that deletion of the chromatin regulator () in the paternal germ line results in elevated tumor incidence in genetically wild type mice. This effect increases following passage through two successive generations of male germline deletion, but is lost following passage through a wild type germ line. The H3K27me3 mark is redistributed in sperm of mutants, and we define approximately 200 H3K27me3-marked regions that exhibit increased DNA methylation, both in sperm of mutants and in somatic tissue of progeny. Hypermethylated regions in enhancers may alter regulation of genes involved in cancer initiation or progression. Epigenetic changes in male gametes may therefore impact cancer susceptibility in adult offspring.

摘要

癌症易感性是可遗传的,但这种遗传性的很大一部分仍然无法解释。一些“缺失”的遗传性可能是由亲代生殖系中的表观遗传变化介导的,这些变化不涉及遗传变异从亲代传递给后代。我们报告说,在父本生殖系中删除染色质调节剂 () 会导致遗传野生型小鼠的肿瘤发病率升高。这种效应在经过两代连续的 雄性生殖系缺失后增加,但在经过野生型生殖系后消失。H3K27me3 标记在 突变体的精子中重新分布,我们定义了大约 200 个 H3K27me3 标记区域,这些区域在 突变体的精子和后代的体细胞组织中表现出 DNA 甲基化增加。增强子中的高甲基化区域可能改变参与癌症起始或进展的基因的调控。因此,雄性配子中的表观遗传变化可能会影响成年后代的癌症易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd5/6456297/d60d906cd913/elife-39380-fig1.jpg

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