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基因组两个功能部分的活性比例是衰老的主要原因。

The Ratio of the Genome Two Functional Parts Activity as the Prime Cause of Aging.

作者信息

Salnikov Lev, Baramiya Mamuka G

机构信息

SibEnzyme US LLC, West Roxbury, MA, United States.

AntiCancer, Inc., San Diego, CA, United States.

出版信息

Front Aging. 2020 Nov 16;1:608076. doi: 10.3389/fragi.2020.608076. eCollection 2020.

Abstract

The genome composes of sets of housekeeping genes (HG) for fundamental cellular autonomous processes and integrative genes (IntG) that provide integrative functions and form the body as an integrated whole. The main paradigm for multicellularity development which has been improved in evolution, is the submission of the cellular autonomy to the interests of the integrated whole. Permanent increase of the "functional tax" of IntG-genome (IntG-shift) and epigenetic restriction of autonomy in phylogenesis/ontogenesis is the essence and root cause of aging, inherent in the very nature of highly integrated multicellularity. The regulation of the balance shift toward HG can be managed to eliminate aging and avoid carcinogenesis, which is only due to the irreversibility of this shift. Here we propose the criterion for measuring the functional and biological age of cells and the body as a whole for assessing the effectiveness of any type of palliative geroprotective or radical anti-aging intervention.

摘要

基因组由用于基本细胞自主过程的管家基因(HG)集和提供整合功能并将身体形成为一个整体的整合基因(IntG)组成。在进化过程中得到改进的多细胞发育的主要范式是将细胞自主性服从于整体的利益。IntG基因组的“功能税”的持续增加(IntG转移)以及系统发育/个体发育中自主性的表观遗传限制是衰老的本质和根本原因,这固有于高度整合的多细胞性的本质之中。可以设法控制向HG的平衡转移以消除衰老并避免致癌作用,这仅仅是由于这种转移的不可逆性。在这里,我们提出了用于测量细胞和整个身体的功能和生物学年龄的标准,以评估任何类型的姑息性老年保护或激进抗衰老干预的有效性。

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本文引用的文献

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A Senescence-Centric View of Aging: Implications for Longevity and Disease.衰老的衰老中心观:对长寿和疾病的影响。
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Changes in DNA repair during aging.衰老过程中DNA修复的变化。
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The evolution of transcriptional regulation in eukaryotes.真核生物转录调控的进化
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