Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.

Germ granules, termed P granules in nematode C. elegans, are the germline-specific cytoplasmic structures widely observed from worms to humans. P granules are known to have critical functions for postembryonic germline development likely through regulating RNA metabolism. They are localized at the p...

Full description

Bibliographic Details
Main Authors: Hyemin Min, Yong-Uk Lee, Yhong-Hee Shim, Ichiro Kawasaki
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-05-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008150
id doaj-eec682183cc14aa7942bccd9d385f3ad
record_format Article
spelling doaj-eec682183cc14aa7942bccd9d385f3ad2021-04-21T14:22:05ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042019-05-01155e100815010.1371/journal.pgen.1008150Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.Hyemin MinYong-Uk LeeYhong-Hee ShimIchiro KawasakiGerm granules, termed P granules in nematode C. elegans, are the germline-specific cytoplasmic structures widely observed from worms to humans. P granules are known to have critical functions for postembryonic germline development likely through regulating RNA metabolism. They are localized at the perinuclear region of germ cells during most of the developmental stages. However, the biological significance of this specific localization remains elusive. PGL-1 and PGL-3, the defining components of P granules, were shown to be lost from the perinuclear region prior to germ cell apoptosis. Furthermore, this loss was shown to be significantly enhanced upon DNA damage. Here, we show that the removal of PGL-1 and PGL-3 from the perinuclear region following UV-induced DNA damage is significantly reduced in autophagy mutants. Autophagy was previously shown to be required for DNA damage-induced germ cell apoptosis. We show that the apoptosis defect of autophagy mutants is bypassed by depletion of pgl-1 or pgl-3. These findings are consistent with time-lapse observations of LGG-1 foci formation, showing that autophagy is activated following UV irradiation and that maximal accumulation of LGG-1 foci occurs before PGL-1 removal. We also show that some of the autophagy genes are transcriptionally activated following UV irradiation by CEP-1, the worm p53-like protein. Taken together, our results indicate that autophagy is required to remove the major P granule components, PGL-1 and PGL-3, and that their removal is required for the full induction of DNA damage-induced germ cell apoptosis. Our study contributes to a better understanding of germ cell apoptosis, a process that leads to the elimination of the vast majority of germ cells in various animals from worms to mammals.https://doi.org/10.1371/journal.pgen.1008150
collection DOAJ
language English
format Article
sources DOAJ
author Hyemin Min
Yong-Uk Lee
Yhong-Hee Shim
Ichiro Kawasaki
spellingShingle Hyemin Min
Yong-Uk Lee
Yhong-Hee Shim
Ichiro Kawasaki
Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.
PLoS Genetics
author_facet Hyemin Min
Yong-Uk Lee
Yhong-Hee Shim
Ichiro Kawasaki
author_sort Hyemin Min
title Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.
title_short Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.
title_full Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.
title_fullStr Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.
title_full_unstemmed Autophagy of germ-granule components, PGL-1 and PGL-3, contributes to DNA damage-induced germ cell apoptosis in C. elegans.
title_sort autophagy of germ-granule components, pgl-1 and pgl-3, contributes to dna damage-induced germ cell apoptosis in c. elegans.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2019-05-01
description Germ granules, termed P granules in nematode C. elegans, are the germline-specific cytoplasmic structures widely observed from worms to humans. P granules are known to have critical functions for postembryonic germline development likely through regulating RNA metabolism. They are localized at the perinuclear region of germ cells during most of the developmental stages. However, the biological significance of this specific localization remains elusive. PGL-1 and PGL-3, the defining components of P granules, were shown to be lost from the perinuclear region prior to germ cell apoptosis. Furthermore, this loss was shown to be significantly enhanced upon DNA damage. Here, we show that the removal of PGL-1 and PGL-3 from the perinuclear region following UV-induced DNA damage is significantly reduced in autophagy mutants. Autophagy was previously shown to be required for DNA damage-induced germ cell apoptosis. We show that the apoptosis defect of autophagy mutants is bypassed by depletion of pgl-1 or pgl-3. These findings are consistent with time-lapse observations of LGG-1 foci formation, showing that autophagy is activated following UV irradiation and that maximal accumulation of LGG-1 foci occurs before PGL-1 removal. We also show that some of the autophagy genes are transcriptionally activated following UV irradiation by CEP-1, the worm p53-like protein. Taken together, our results indicate that autophagy is required to remove the major P granule components, PGL-1 and PGL-3, and that their removal is required for the full induction of DNA damage-induced germ cell apoptosis. Our study contributes to a better understanding of germ cell apoptosis, a process that leads to the elimination of the vast majority of germ cells in various animals from worms to mammals.
url https://doi.org/10.1371/journal.pgen.1008150
work_keys_str_mv AT hyeminmin autophagyofgermgranulecomponentspgl1andpgl3contributestodnadamageinducedgermcellapoptosisincelegans
AT yonguklee autophagyofgermgranulecomponentspgl1andpgl3contributestodnadamageinducedgermcellapoptosisincelegans
AT yhongheeshim autophagyofgermgranulecomponentspgl1andpgl3contributestodnadamageinducedgermcellapoptosisincelegans
AT ichirokawasaki autophagyofgermgranulecomponentspgl1andpgl3contributestodnadamageinducedgermcellapoptosisincelegans
_version_ 1714668481051361280