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人类卫星 III(1q12)拷贝数变异在衰老、应激和病理过程中的适应性反应中的作用:钟摆模型。

The Role of Human Satellite III (1q12) Copy Number Variation in the Adaptive Response during Aging, Stress, and Pathology: A Pendulum Model.

机构信息

Laboratory of Molecular Biology, Research Centre for Medical Genetics, 115478 Moscow, Russia.

出版信息

Genes (Basel). 2021 Sep 28;12(10):1524. doi: 10.3390/genes12101524.

Abstract

The pericentric satellite III (SatIII or Sat3) and II tandem repeats recently appeared to be transcribed under stress conditions, and the transcripts were shown to play an essential role in the universal stress response. In this paper, we review the role of human-specific SatIII copy number variation (CNV) in normal stress response, aging and pathology, with a focus on 1q12 loci. We postulate a close link between transcription of SatII/III repeats and their CNV. The accrued body of data suggests a hypothetical universal mechanism, which provides for SatIII copy gain during the stress response, alongside with another, more hypothetical reverse mechanism that might reduce the mean SatIII copy number, likely via the selection of cells with excessively large 1q12 loci. Both mechanisms, working alternatively like swings of the pendulum, may ensure the balance of SatIII copy numbers and optimum stress resistance. This model is verified on the most recent data on SatIII CNV in pathology and therapy, aging, senescence and response to genotoxic stress in vitro.

摘要

着丝粒卫星 III(SatIII 或 Sat3)和 II 串联重复序列最近似乎在应激条件下被转录,其转录本在普遍应激反应中发挥着重要作用。本文综述了人类特异性 SatIII 拷贝数变异(CNV)在正常应激反应、衰老和病理学中的作用,重点关注 1q12 位。我们推测 SatII/III 重复序列的转录与其 CNV 之间存在密切联系。越来越多的数据表明存在一种假设的普遍机制,该机制在应激反应期间提供 SatIII 拷贝数增加,同时存在另一种更假设的反向机制,可能通过选择具有过大 1q12 位的细胞来降低平均 SatIII 拷贝数。这两种机制,像钟摆的摆动一样交替工作,可能确保 SatIII 拷贝数的平衡和最佳的应激抵抗能力。该模型在 SatIII CNV 在病理学和治疗、衰老、衰老和体外对遗传毒性应激反应的最新数据中得到验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5710/8535310/4116a3f31932/genes-12-01524-g001.jpg

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