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Proteinase K is an activator for the male-dependent spermiogenesis pathway in Caenorhabditis elegans: Its application to pharmacological dissection of spermiogenesis.

Authors :
Tajima T
Ogawa F
Nakamura S
Hashimoto M
Omote M
Nishimura H
Source :
Genes to cells : devoted to molecular & cellular mechanisms [Genes Cells] 2019 Mar; Vol. 24 (3), pp. 244-258. Date of Electronic Publication: 2019 Feb 13.
Publication Year :
2019

Abstract

Caenorhabditis elegans spermiogenesis involves spermatid activation into spermatozoa. Activation occurs through either SPE-8 class-dependent or class-independent pathways. Pronase (Pron) activates the SPE-8 class-dependent pathway, whereas no in vitro tools are available to stimulate the SPE-8 class-independent pathway. Thus, whether there is a functional relationship between these two pathways is currently unclear. In this study, we found that proteinase K (ProK) can activate the SPE-8 class-independent pathway. In vitro spermiogenesis assays using Pron and ProK suggested that SPE-8 class proteins act in the hermaphrodite- and male-dependent spermiogenesis pathways and that some spermatid proteins presumably working downstream of spermiogenesis pathways, including MAP kinases, are preferentially involved in the SPE-8 class-dependent pathway. We screened a library of chemicals, and a compound that we named DDI-1 inhibited both Pron- and ProK-induced spermiogenesis. To our surprise, several DDI-1 analogues that are structurally similar to DDI-1 blocked Pron, but not ProK, induced spermiogenesis. Although the mechanism by which DDI-1 blocks spermiogenesis is yet unknown, we have begun to address this issue by selecting two DDI-1-resistant mutants. Collectively, our data support a model in which C. elegans male and hermaphrodite spermiogenesis each has its own distinct, parallel pathway.<br /> (© 2019 Molecular Biology Society of Japan and John Wiley & Sons Australia, Ltd.)

Details

Language :
English
ISSN :
1365-2443
Volume :
24
Issue :
3
Database :
MEDLINE
Journal :
Genes to cells : devoted to molecular & cellular mechanisms
Publication Type :
Academic Journal
Accession number :
30656805
Full Text :
https://doi.org/10.1111/gtc.12670