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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Main Authors: Lu Wang, Fei Xu, Guishuan Wang, Xiaorong Wang, Ajuan Liang, Hefeng Huang, Fei Sun
Format: Article
Language:English
Published: SpringerOpen 2016-09-01
Series:Protein & Cell
Subjects:
Online Access:http://link.springer.com/article/10.1007/s13238-016-0308-z
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spelling 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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