Somatic PMK-1/p38 signaling links environmental stress to germ cell apoptosis and heritable euploidy.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35121747.
- Also identified by DOI 10.1038/s41467-022-28225-8 and PMC identifier 8816960.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Inheritance of stable and euploid genomes is a prerequisite for species maintenance. The DNA damage response in germ cells controls the integrity of heritable genomes. Whether and how somatic stress responses impact the quality control of germline genomes has remained unclear. Here, we show that PMK-1/p38-mediated stress signaling in intestinal cells is required for germ cell apoptosis amid ionizing radiation (IR)-induced or meiotic DNA double strand breaks (DSBs) in C. elegans. We demonstrate that intestinal PMK-1/p38 signaling regulates the germ cell death in response to environmental stress. The PMK-1/p38 target SYSM-1 is secreted from the intestine into the germline to trigger apoptosis of meiotic pachytene cells. Compromised PMK-1/p38 signaling in intestinal cells leads to stress-induced aneuploidy in the consequent generation. Our data suggest that somatic stress surveillance controls heritable genome integrity and euploidy.
Medical subject headings
- Aneuploidy
- Apoptosis
- Caenorhabditis elegans
- Caenorhabditis elegans Proteins
- Germ Cells
- MAP Kinase Signaling System
- Mitogen-Activated Protein Kinases
- Stress, Physiological