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额外染色体的后果。

Consequences of gaining an extra chromosome.

机构信息

Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA.

出版信息

Chromosome Res. 2023 Aug 25;31(3):24. doi: 10.1007/s10577-023-09732-w.

Abstract

Mistakes in chromosome segregation leading to aneuploidy are the primary cause of miscarriages in humans. Excluding sex chromosomes, viable aneuploidies in humans include trisomies of chromosomes 21, 18, or 13, which cause Down, Edwards, or Patau syndromes, respectively. While individuals with trisomy 18 or 13 die soon after birth, people with Down syndrome live to adulthood but have intellectual disabilities and are prone to multiple diseases. At the cellular level, mistakes in the segregation of a single chromosome leading to a cell losing a chromosome are lethal. In contrast, the cell that gains a chromosome can survive. Several studies support the hypothesis that gaining an extra copy of a chromosome causes gene-specific phenotypes and phenotypes independent of the identity of the genes encoded within that chromosome. The latter, referred to as aneuploidy-associated phenotypes, are the focus of this review. Among the conserved aneuploidy-associated phenotypes observed in yeast and human cells are lower viability, increased gene expression, increased protein synthesis and turnover, abnormal nuclear morphology, and altered metabolism. Notably, abnormal nuclear morphology of aneuploid cells is associated with increased metabolic demand for de novo synthesis of sphingolipids. These findings reveal important insights into the possible pathological role of aneuploidy in Down syndrome. Despite the adverse effects on cell physiology, aneuploidy is a hallmark of cancer cells. Understanding how aneuploidy affects cell physiology can reveal insights into the selective pressure that aneuploid cancer cells must overcome to support unlimited proliferation.

摘要

染色体分离错误导致非整倍体是人类流产的主要原因。除性染色体外,人类可存活的非整倍体包括 21 号、18 号或 13 号染色体的三体,分别导致唐氏综合征、爱德华氏综合征或帕陶氏综合征。虽然 18 三体或 13 三体的个体在出生后不久就会死亡,但唐氏综合征患者可以活到成年,但存在智力障碍,并且容易患上多种疾病。在细胞水平上,导致细胞丢失一条染色体的单个染色体分离错误是致命的。相比之下,获得一条额外染色体的细胞可以存活。几项研究支持这样一种假设,即获得额外的染色体拷贝会导致基因特异性表型和独立于该染色体上编码的基因身份的表型。后者被称为非整倍体相关表型,是本综述的重点。在酵母和人类细胞中观察到的保守非整倍体相关表型包括较低的存活率、增加的基因表达、增加的蛋白质合成和周转、异常的核形态和改变的代谢。值得注意的是,非整倍体细胞的异常核形态与从头合成鞘脂的新合成代谢需求增加有关。这些发现揭示了非整倍体在唐氏综合征中可能的病理作用的重要见解。尽管对细胞生理学有不利影响,但非整倍体是癌细胞的标志。了解非整倍体如何影响细胞生理学可以揭示对非整倍体癌细胞必须克服以支持无限增殖的选择压力的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d43a/10449985/2aeb9a757f34/10577_2023_9732_Fig1_HTML.jpg

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