TY - JOUR
T1 - Gonadotropin-releasing hormone-like receptor 2 inversely regulates somatic proteostasis and reproduction in Caenorhabditis elegans
AU - Kishner, Mor
AU - Habaz, Libat
AU - Meshnik, Lana
AU - Meidan, Tomer Dvir
AU - Polonsky, Alexandra
AU - Ben-Zvi, Anat
N1 - Funding Information:
We thank Prof. Isabel Beets for sharing unpublished data and discussions. Some nematode strains used in this work were provided by the Caenorhabditis Genetics Center, which is funded by the NIH National Center for Research Resources (NCRR).
Funding Information:
This study was funded by the Binational Science Foundation (BSF) grant 2017241 to AB-Z. MK was supported by the Ministry of Science and Technology, Levi Eshkol Ph.D. fellowship (3-16593). LM was supported by the Ministry of Science and Technology, Yitzhak Navon Ph.D. fellowship (3-16627), and Kreitman Biotech scholarship.
Publisher Copyright:
Copyright © 2022 Kishner, Habaz, Meshnik, Meidan, Polonsky and Ben-Zvi.
PY - 2022/8/29
Y1 - 2022/8/29
N2 - The quality control machinery regulates the cellular proteome to ensure proper protein homeostasis (proteostasis). In Caenorhabditis elegans, quality control networks are downregulated cell-nonautonomously by the gonadal longevity pathway or metabolic signaling at the onset of reproduction. However, how signals are mediated between the gonad and the somatic tissues is not known. Gonadotropin-releasing hormone (GnRH)-like signaling functions in the interplay between development and reproduction and have conserved roles in regulating reproduction, metabolism, and stress. We, therefore, asked whether GnRH-like signaling is involved in proteostasis collapse at the onset of reproduction. Here, we examine whether C. elegans orthologues of GnRH receptors modulate heat shock survival. We find that gnrr-2 is required for proteostasis remodeling in different somatic tissues during the transition to adulthood. We show that gnrr-2 likely functions in neurons downstream of the gonad in the gonadal-longevity pathway and modulate the somatic regulation of transcription factors HSF-1, DAF-16, and PQM-1. In parallel, gnrr-2 modulates egg-laying rates, vitellogenin production, and thus reproductive capacity. Taken together, our data suggest that gnrr-2 plays a GnRH-associated role, mediating the cross-talk between the reproduction system and the soma in the decision to commit to reproduction.
AB - The quality control machinery regulates the cellular proteome to ensure proper protein homeostasis (proteostasis). In Caenorhabditis elegans, quality control networks are downregulated cell-nonautonomously by the gonadal longevity pathway or metabolic signaling at the onset of reproduction. However, how signals are mediated between the gonad and the somatic tissues is not known. Gonadotropin-releasing hormone (GnRH)-like signaling functions in the interplay between development and reproduction and have conserved roles in regulating reproduction, metabolism, and stress. We, therefore, asked whether GnRH-like signaling is involved in proteostasis collapse at the onset of reproduction. Here, we examine whether C. elegans orthologues of GnRH receptors modulate heat shock survival. We find that gnrr-2 is required for proteostasis remodeling in different somatic tissues during the transition to adulthood. We show that gnrr-2 likely functions in neurons downstream of the gonad in the gonadal-longevity pathway and modulate the somatic regulation of transcription factors HSF-1, DAF-16, and PQM-1. In parallel, gnrr-2 modulates egg-laying rates, vitellogenin production, and thus reproductive capacity. Taken together, our data suggest that gnrr-2 plays a GnRH-associated role, mediating the cross-talk between the reproduction system and the soma in the decision to commit to reproduction.
KW - C. elegans
KW - aging
KW - gonadal longevity signaling
KW - gonadotropin-releasing hormone (GnRH/GnRH receptor)
KW - proteostasis
KW - reproduction
KW - stress response
UR - http://www.scopus.com/inward/record.url?scp=85138097504&partnerID=8YFLogxK
U2 - 10.3389/fcell.2022.951199
DO - 10.3389/fcell.2022.951199
M3 - Article
C2 - 36105349
AN - SCOPUS:85138097504
SN - 2296-634X
VL - 10
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 951199
ER -