PMK-1 p38 MAPK promotes cadmium stress resistance, the expression of SKN-1/Nrf and DAF-16 target genes, and protein biosynthesis in Caenorhabditis elegans

Keshet A., Mertenskötter A., Winter S., Brinkmann V., Dölling R., Paul R.

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

The mechanisms of cadmium (Cd) resistance are complex and not sufficiently understood. The present study, therefore, aimed at assessing the roles of important components of stress-signaling pathways and of ABC transporters under severe Cd stress in Caenorhabditis elegans. Survival assays on mutant and control animals revealed a significant promotion of Cd resistance by the PMK-1 p38 MAP kinase, the transcription factor DAF-16/FoxO, and the ABC transporter MRP-1. Transcriptome profiling by RNA-Seq on wild type and a pmk-1 mutant under control and Cd stress conditions revealed, inter alia, a PMK-1-dependent promotion of gene expression for the translational machinery. PMK-1 also promoted the expression of target genes of the transcription factors SKN-1/Nrf and DAF-16 in Cd-stressed animals, which included genes for molecular chaperones or immune proteins. Gene expression studies by qRT-PCR confirmed the positive effects of PMK-1 on DAF-16 activity under Cd stress and revealed negative effects of DAF-16 on the expression of genes for MRP-1 and DAF-15/raptor. Additional studies on pmk-1 RNAi-treated wild type and mutant strains provided further information on the effects of PMK-1 on SKN-1 and DAF-16, which resulted in a model of these relationships. The results of this study demonstrate a central role of PMK-1 for the processing of cellular responses to abiotic and biotic stressors, with the promoting effects of PMK-1 on Cd resistance mostly mediated by the transcription factors SKN-1 and DAF-16.

Details zur Publikation

FachzeitschriftMolecular Genetics and Genomics
Jahrgang / Bandnr. / Volume292
Ausgabe / Heftnr. / Issue6
Seitenbereich1341-1361
StatusVeröffentlicht
Veröffentlichungsjahr2017
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1007/s00438-017-1351-z
Link zum Volltexthttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026521659&origin=inward
StichwörterGlutathione; Metallothionein; Molecular chaperones; RNA-Seq; TOR signaling; Transcriptome

Autor*innen der Universität Münster

Paul, Rüdiger J.
Professur für Zoophysiologie (Prof. Zeis)