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端粒动力学:叶酸和 DNA 甲基化的影响。

Telomere dynamics: the influence of folate and DNA methylation.

机构信息

CSIRO Food and Nutritional Sciences Division, Adelaide, South Australia.

出版信息

Ann N Y Acad Sci. 2011 Jul;1229:76-88. doi: 10.1111/j.1749-6632.2011.06101.x.

Abstract

Since the suggestion of their existence, a wealth of literature on telomere biology has emerged aimed at solving the DNA end-underreplication problem identified by Olovnikov in 1971. Telomere shortening/dysfunction is now recognized as increasing degenerative disease risk. Recent studies have suggested that both dietary patterns and individual micronutrients--including folate--can influence telomere length and function. Folate is an important dietary vitamin required for DNA synthesis, repair, and one-carbon metabolism within the cell. However, the potential mechanisms by which folate deficiency directly or indirectly affects telomere biology has not yet been reviewed comprehensively. The present review summarizes recent published knowledge and identifies the residual knowledge gaps. Specifically, this review addresses whether it is plausible that folate deficiency may (1) cause accelerated telomere shortening, (2) intrinsically affect telomere function, and/or (3) cause increased telomere-end fusions and subsequent breakage-fusion-bridge cycles in the cell.

摘要

自端粒生物学的存在被提出以来,大量的文献已经涌现出来,旨在解决 1971 年由 Olovnikov 所提出的 DNA 末端复制不足问题。端粒缩短/功能障碍现已被认为会增加退行性疾病的风险。最近的研究表明,饮食模式和个体微量营养素——包括叶酸——都可以影响端粒的长度和功能。叶酸是细胞内 DNA 合成、修复和一碳代谢所必需的重要膳食维生素。然而,叶酸缺乏直接或间接影响端粒生物学的潜在机制尚未得到全面综述。本综述总结了最近发表的知识,并确定了剩余的知识空白。具体而言,本综述探讨了叶酸缺乏是否可能:(1)导致端粒缩短加速,(2)内在影响端粒功能,和/或(3)导致细胞中端粒末端融合和随后的断裂-融合-桥循环增加。

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