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端粒磨损与年龄相关,导致端粒附近区域的基因表达异常。

Age-related telomere attrition causes aberrant gene expression in sub-telomeric regions.

机构信息

Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.

Institute on the Biology of Aging and Metabolism, Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, USA.

出版信息

Aging Cell. 2021 Jun;20(6):e13357. doi: 10.1111/acel.13357. Epub 2021 May 21.

Abstract

Telomere attrition has been proposed as a biomarker and causal factor in aging. In addition to causing cellular senescence and apoptosis, telomere shortening has been found to affect gene expression in subtelomeric regions. Here, we analyzed the distribution of age-related differentially expressed genes from the GTEx RNA sequencing database of 54 tissue types from 979 human subjects and found significantly more upregulated than downregulated genes in subtelomeric regions as compared to the genome-wide average. Our data demonstrate spatial relationships between telomeres and gene expression in aging.

摘要

端粒磨损被认为是衰老的生物标志物和原因。除了导致细胞衰老和凋亡外,端粒缩短已被发现会影响端粒附近区域的基因表达。在这里,我们分析了来自 979 个人类样本的 54 种组织类型的 GTEx RNA 测序数据库中与年龄相关的差异表达基因的分布,发现与全基因组平均值相比,端粒附近区域的上调基因明显多于下调基因。我们的数据证明了端粒与衰老过程中基因表达之间的空间关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1398/8208793/b2538ed17e33/ACEL-20-e13357-g004.jpg

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