C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans
ABSTRACT Reproduction, fat metabolism, and longevity are intertwined regulatory axes; recent studies in C. elegans have provided evidence that these processes are directly coupled. However, the mechanisms by which they are coupled and the reproductive signals modulating fat metabolism and lifespan a...
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doaj-aa74b8c100f3409b911f1a3cea9358392020-11-25T00:46:26ZengSpringerOpenProtein & Cell1674-800X1674-80182016-09-0171071472110.1007/s13238-016-0308-zC30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegansLu Wang0Fei Xu1Guishuan Wang2Xiaorong Wang3Ajuan Liang4Hefeng Huang5Fei Sun6International Peace Maternity & Child Health Hospital, Shanghai Key laboratory for Reproductive Medicine, School of Medicine, Institute of Embryo-Fetal Original Adult Disease, Shanghai Jiaotong UniversitySchool of Life Sciences, University of Science and Technology of ChinaInternational Peace Maternity & Child Health Hospital, Shanghai Key laboratory for Reproductive Medicine, School of Medicine, Institute of Embryo-Fetal Original Adult Disease, Shanghai Jiaotong UniversityInternational Peace Maternity & Child Health Hospital, Shanghai Key laboratory for Reproductive Medicine, School of Medicine, Institute of Embryo-Fetal Original Adult Disease, Shanghai Jiaotong UniversityInternational Peace Maternity & Child Health Hospital, Shanghai Key laboratory for Reproductive Medicine, School of Medicine, Institute of Embryo-Fetal Original Adult Disease, Shanghai Jiaotong UniversityInternational Peace Maternity & Child Health Hospital, Shanghai Key laboratory for Reproductive Medicine, School of Medicine, Institute of Embryo-Fetal Original Adult Disease, Shanghai Jiaotong UniversityInternational Peace Maternity & Child Health Hospital, Shanghai Key laboratory for Reproductive Medicine, School of Medicine, Institute of Embryo-Fetal Original Adult Disease, Shanghai Jiaotong UniversityABSTRACT Reproduction, fat metabolism, and longevity are intertwined regulatory axes; recent studies in C. elegans have provided evidence that these processes are directly coupled. However, the mechanisms by which they are coupled and the reproductive signals modulating fat metabolism and lifespan are poorly understood. Here, we find that an oogenesis-enriched gene, c30f12.4, is specifically expressed and located in germ cells and early embryos; when the gene is knocked out, oogenesis is disrupted and brood size is decreased. In addition to the reproductive phenotype, we find that the loss of c30f12.4 alters fat metabolism, resulting in decreased fat storage and smaller lipid droplets. Meanwhile, c30f12.4 mutant worms display a shortened lifespan. Our results highlight an important role for c30f12.4 in regulating reproduction, fat homeostasis, and aging in C. elegans, which helps us to better understand the relationship between these processes.http://link.springer.com/article/10.1007/s13238-016-0308-zC30F12.4oogenesisfat metabolismlifespan |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lu Wang Fei Xu Guishuan Wang Xiaorong Wang Ajuan Liang Hefeng Huang Fei Sun |
spellingShingle |
Lu Wang Fei Xu Guishuan Wang Xiaorong Wang Ajuan Liang Hefeng Huang Fei Sun C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans Protein & Cell C30F12.4 oogenesis fat metabolism lifespan |
author_facet |
Lu Wang Fei Xu Guishuan Wang Xiaorong Wang Ajuan Liang Hefeng Huang Fei Sun |
author_sort |
Lu Wang |
title |
C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans |
title_short |
C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans |
title_full |
C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans |
title_fullStr |
C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans |
title_full_unstemmed |
C30F12.4 influences oogenesis, fat metabolism, and lifespan in C. elegans |
title_sort |
c30f12.4 influences oogenesis, fat metabolism, and lifespan in c. elegans |
publisher |
SpringerOpen |
series |
Protein & Cell |
issn |
1674-800X 1674-8018 |
publishDate |
2016-09-01 |
description |
ABSTRACT Reproduction, fat metabolism, and longevity are intertwined regulatory axes; recent studies in C. elegans have provided evidence that these processes are directly coupled. However, the mechanisms by which they are coupled and the reproductive signals modulating fat metabolism and lifespan are poorly understood. Here, we find that an oogenesis-enriched gene, c30f12.4, is specifically expressed and located in germ cells and early embryos; when the gene is knocked out, oogenesis is disrupted and brood size is decreased. In addition to the reproductive phenotype, we find that the loss of c30f12.4 alters fat metabolism, resulting in decreased fat storage and smaller lipid droplets. Meanwhile, c30f12.4 mutant worms display a shortened lifespan. Our results highlight an important role for c30f12.4 in regulating reproduction, fat homeostasis, and aging in C. elegans, which helps us to better understand the relationship between these processes. |
topic |
C30F12.4 oogenesis fat metabolism lifespan |
url |
http://link.springer.com/article/10.1007/s13238-016-0308-z |
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