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DNA Mismatch Repair System: Repercussions in Cellular Homeostasis and Relationship with Aging

机译:DNA错配修复系统:细胞稳态的影响及其与衰老的关系

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The mechanisms that concern DNA repair have been studied in the last years due to their consequences in cellular homeostasis. The diverse and damaging stimuli that affect DNA integrity, such as changes in the genetic sequence and modifications in gene expression, can disrupt the steady state of the cell and have serious repercussions to pathways that regulate apoptosis, senescence, and cancer. These altered pathways not only modify cellular and organism longevity, but quality of life (“health-span”). The DNA mismatch repair system (MMR) is highly conserved between species; its role is paramount in the preservation of DNA integrity, placing it as a necessary focal point in the study of pathways that prolong lifespan, aging, and disease. Here, we review different insights concerning the malfunction or absence of the DNA-MMR and its impact on cellular homeostasis. In particular, we will focus on DNA-MMR mechanisms regulated by known repair proteins MSH2, MSH6, PMS2, and MHL1, among others.
机译:近年来,由于DNA修复会引起细胞动态平衡,因此已经研究了有关DNA修复的机制。影响DNA完整性的各种破坏性刺激,例如遗传序列的变化和基因表达的修饰,可能破坏细胞的稳态,并对调节细胞凋亡,衰老和癌症的途径产生严重影响。这些改变的途径不仅改变细胞和生物的寿命,而且改变生活质量(“健康跨度”)。 DNA错配修复系统(MMR)在物种之间是高度保守的。它在保持DNA完整性方面的作用至关重要,将其作为延长寿命,衰老和疾病的途径研究的必要重点。在这里,我们审查有关DNA-MMR的故障或缺失及其对细胞稳态的影响的不同见解。特别是,我们将专注于受已知修复蛋白MSH2,MSH6,PMS2和MHL1等调控的DNA-MMR机制。

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