Tetz George, Tetz Victor
Human Microbiology Institute, 423 West 127 Street, New York, NY, 10027, USA.
Theory Biosci. 2018 Nov;137(2):145-154. doi: 10.1007/s12064-018-0267-4. Epub 2018 Jul 5.
Here, we present new theory and law of longevity intended to evaluate fundamental factors that control lifespan. This theory is based on the fact that genes affecting host organism longevity are represented by subpopulations: genes of host eukaryotic cells, commensal microbiota, and non-living genetic elements. Based on Tetz's theory of longevity, we propose that lifespan and aging are defined by the accumulation of alterations over all genes of macroorganism and microbiome and the non-living genetic elements associated with them. Tetz's law of longevity states that longevity is limited by the accumulation of alterations to the limiting value that is not compatible with life. Based on theory and law, we also propose a novel model to calculate several parameters, including the rate of aging and the remaining lifespan of individuals. We suggest that this theory and model have explanatory and predictive potential to eukaryotic organisms, allowing the influence of diseases, medication, and medical procedures to be re-examined in relation to longevity. Such estimates also provide a framework to evaluate new fundamental aspects that control aging and lifespan.
在此,我们提出了旨在评估控制寿命的基本因素的新的长寿理论和定律。该理论基于这样一个事实,即影响宿主生物体寿命的基因由亚群代表:宿主真核细胞基因、共生微生物群和非生命遗传元件。基于特茨的长寿理论,我们提出寿命和衰老由宏观生物体和微生物组的所有基因以及与之相关的非生命遗传元件的变化积累所定义。特茨的长寿定律指出,长寿受到变化积累到与生命不相容的极限值的限制。基于该理论和定律,我们还提出了一个新模型来计算几个参数,包括衰老速率和个体的剩余寿命。我们认为,该理论和模型对真核生物具有解释和预测潜力,能够重新审视疾病、药物和医疗程序对长寿的影响。此类估计还提供了一个框架,用于评估控制衰老和寿命的新的基本方面。