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Caenorhabditis elegans homologue of Fam210 is required for oogenesis and reproduction
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作者 Jing Kang hengda zhou +5 位作者 Fengxiu Sun Yongtian Chen Jianzhi Zhao Wei-Jun Yang Suhong Xu Caiyong Chen 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2020年第11期694-704,共11页
Mitochondria are the central hub for many metabolic processes,including the citric acid cycle,oxidative phosphorylation,and fatty acid oxidation.Recent studies have identified a new mitochondrial protein family,Fam210... Mitochondria are the central hub for many metabolic processes,including the citric acid cycle,oxidative phosphorylation,and fatty acid oxidation.Recent studies have identified a new mitochondrial protein family,Fam210,that regulates bone metabolism and red cell development in vertebrates.The model organism Caenorhabditis elegans has a Fam210 gene,y56a3a.22,but it lacks both bones and red blood cells.In this study,we report that Y56A3A.22 plays a crucial role in regulating mitochondrial protein homeostasis and reproduction.The nematode y56a3a.22 is expressed in various tissues,including the intestine,muscle,hypodermis,and germline,and its encoded protein is predominantly localized in mitochondria.y56a3a.22 deletion mutants are sterile owing to impaired oogenesis.Loss of Y56A3A.22 induced mitochondrial unfolded protein response(UPRmt),which is mediated through the ATFS-1-dependent pathway,in tissues such as the intestine,germline,hypodermis,and vulval muscle.We further show that infertility and UPRmt induces by Y56A3A.22 deficiency are not attributed to systemic iron deficiency.Together,our study reveals an important role of Y56A3A.22 in regulating mitochondrial protein homeostasis and oogenesis and provides a new genetic tool for exploring the mechanisms regulating mitochondrial metabolism and reproduction as well as the fundamental role of the Fam210 family. 展开更多
关键词 OOGENESIS Iron metabolism Mitochondrial protein homeostasis FERRITIN REPRODUCTION C.elegans
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