| Literature DB >> 31823348 |
Guoping Dong1, Zhe Zhang1, Kun Duan1, Wenpeng Shi1, Rui Huang1, Bangjun Wang1, Lingfei Luo1, Yaoguang Zhang1, Hua Ruan1, Honghui Huang1.
Abstract
Beclin 1/Atg6 is an essential autophagy gene, and deficiency of this gene in organisms leads to impaired autophagic flux, usually with cell apoptosis; however, the causative mechanism of cell apoptosis is not clear. Here, we knocked out the beclin 1 gene in zebrafish and found that autophagic flux is disrupted in mutants. Beclin 1-deficient zebrafish live through embryogenesis but die at larval stage. We found accumulated protein aggregates and vigorous apoptosis in mutant larvae, predominantly in the liver. The hepatic cell apoptosis in mutants results from an endoplasmic reticulum (ER) stress response; however, it is not the leading cause of mutant larval lethality. Our work proposes that ER stress induces cell apoptosis in Beclin 1-deficient organisms.Entities:
Keywords: Beclin 1; ER stress; autophagy; cell apoptosis; protein aggregates; zebrafish
Year: 2019 PMID: 31823348 DOI: 10.1002/1873-3468.13712
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124