Kogod Center on Aging and Division of Endocrinology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.
Department of Trauma, Orthopedics and Reconstructive Surgery, Georg-August-University of Goettingen, 37075 Goettingen, Germany.
Int J Mol Sci. 2021 Jan 2;22(1):401. doi: 10.3390/ijms22010401.
Aging represents the multifactorial decline in physiological function of every living organism. Over the past decades, several hallmarks of aging have been defined, including epigenetic deregulation. Indeed, multiple epigenetic events were found altered across different species during aging. Epigenetic changes directly contributing to aging and aging-related diseases include the accumulation of histone variants, changes in chromatin accessibility, loss of histones and heterochromatin, aberrant histone modifications, and deregulated expression/activity of miRNAs. As a consequence, cellular processes are affected, which results in the development or progression of several human pathologies, including cancer, diabetes, osteoporosis, and neurodegenerative disorders. In this review, we focus on epigenetic mechanisms underlying aging-related processes in various species and describe how these deregulations contribute to human diseases.
衰老是指每个生物体的生理功能多因素下降。在过去的几十年中,已经定义了几种衰老的标志,包括表观遗传失调。事实上,在衰老过程中,不同物种中发现了多种表观遗传事件的改变。直接导致衰老和与衰老相关疾病的表观遗传变化包括组蛋白变体的积累、染色质可及性的改变、组蛋白和异染色质的丢失、异常的组蛋白修饰以及 miRNA 的表达/活性失调。因此,细胞过程受到影响,导致几种人类疾病的发展或进展,包括癌症、糖尿病、骨质疏松症和神经退行性疾病。在这篇综述中,我们重点介绍了各种物种中与衰老相关过程相关的表观遗传机制,并描述了这些失调如何导致人类疾病。