학술논문
Autophagy impairment and lifespan reduction caused by Atg1 RNAi or Atg18 RNAi expression in adult fruit flies (Drosophila melanogaster).
Document Type
Article
Author
Bierlein, Mariah; Charles, Joseph; Polisuk-Balfour, Trevor; Bretscher, Heidi; Rice, Micaela; Zvonar, Jacklyn; Pohl, Drake; Winslow, Lindsey; Wasie, Brennah; Deurloo, Sara; Van Wert, Jordan; Williams, Britney; Ankney, Gabrielle; Harmon, Zachary; Dann, Erica; Azuz, Anna; Guzman-Vargas, Alex; Kuhns, Elizabeth; Neufeld, Thomas P.; O'Connor, Michael B.
Source
Subject
*BIOLOGICAL models
*LYSOSOMES
*AUTOPHAGY
*ANIMAL experimentation
*FLIES
*HUMAN life cycle
*ORGANELLES
*GENE expression
*RISK assessment
*RESEARCH funding
*GENES
*FAT cells
*LONGEVITY
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Language
ISSN
0016-6731
Abstract
Autophagy, an autophagosome and lysosome-based eukaryotic cellular degradation system, has previously been implicated in lifespan regulation in different animal models. In this report, we show that expression of the RNAi transgenes targeting the transcripts of the key autophagy genes Atg1 or Atg18 in adult fly muscle or glia does not affect the overall levels of autophagosomes in those tissues and does not change the lifespan of the tested flies but the lifespan reduction phenotype has become apparent when Atg1 RNAi or Atg18 RNAi is expressed ubiquitously in adult flies or after autophagy is eradicated through the knockdown of Atg1 or Atg18 in adult fly adipocytes. Lifespan reduction was also observed when Atg1 or Atg18 was knocked down in adult fly enteroblasts and midgut stem cells. Overexpression of wild-type Atg1 in adult fly muscle or adipocytes reduces the lifespan and causes accumulation of high levels of ubiquitinated protein aggregates in muscles. Our research data have highlighted the important functions of the key autophagy genes in adult fly adipocytes, enteroblasts, and midgut stem cells and their undetermined roles in adult fly muscle and glia for lifespan regulation. [ABSTRACT FROM AUTHOR]