Nanjing Agricultural University, Nanjing, China.
Huazhong University of Science and Technology, Wuhan, China.
Adv Exp Med Biol. 2021;1208:175-190. doi: 10.1007/978-981-16-2830-6_10.
Macroautophagy (referred to as autophagy hereafter) is a highly conserved catabolic process in eukaryotic cells. Autophagy is essential for cellular homeostasis through elimination and recycling of large cytoplasmic components, such as abnormal protein aggregates and damaged organelles, via lysosomal degradation. Since being originally identified by genetic screening in yeast, autophagy-related (ATG) genes have played a central role in autophagy research in different organisms, including plants, worms, flies, and mammals. Mouse models for monitoring autophagic activity or clarifying its biological functions have also been established. These mice are powerful tools to investigate roles of autophagy in vivo. Owing to the rapid technological advances in molecular biology, it is ever more efficient and simpler to manipulate autophagy-associated genes. Herein, we will introduce some commonly used approaches of gene silencing in mammalian cells, including CRIPSR/Cas9-mediated gene knockout and siRNA- and shRNA-mediated gene knockdown. We also summarized the common mouse models used for assessing autophagy. We hope to bring the researchers some useful information as they study autophagy.
自噬(简称自噬)是真核细胞中一种高度保守的分解代谢过程。通过溶酶体降解,自噬可以清除和回收细胞质中的大成分,如异常蛋白聚集体和受损细胞器,从而在细胞内稳态中发挥重要作用。自噬相关(ATG)基因自最初在酵母中通过遗传筛选被鉴定以来,在包括植物、蠕虫、苍蝇和哺乳动物在内的不同生物体的自噬研究中发挥了核心作用。还建立了用于监测自噬活性或阐明其生物学功能的小鼠模型。这些小鼠是研究体内自噬作用的有力工具。由于分子生物学技术的快速发展,操纵与自噬相关的基因变得更加高效和简单。本文将介绍一些常用的哺乳动物细胞基因沉默方法,包括 CRISPR/Cas9 介导的基因敲除和 siRNA 和 shRNA 介导的基因敲低。我们还总结了用于评估自噬的常见小鼠模型。希望这些信息能为研究自噬的研究人员提供一些有用的参考。