Abstract

In the ascidian Ciona robusta (formerly C. intestinalis type A), the mechanism underlying sperm penetration through the egg investment remains unknown. We previously reported that proteins containing both an astacin metalloprotease domain and thrombospondin type 1 repeats are abundant in the sperm surface protein-enriched fraction of C. robusta. Here we investigated the involvement of those proteins in fertilisation. We refined the sequences of astacin metalloproteases, confirmed that five of them are present in the sperm, and labelled them as tunicate astacin and thrombospondin type 1 repeat-containing (Tast) proteins. Fertilisation of C. robusta eggs was potently inhibited by a metalloprotease inhibitor GM6001. The eggs cleaved normally when they were vitelline coat-free or the inhibitor was added after insemination. Furthermore, vitelline coat proteins were degraded after incubation with intact sperm. These results suggest that sperm metalloproteases are indispensable for fertilisation, probably owing to direct or indirect mediation of vitelline-coat digestion during sperm penetration. TALEN-mediated knockout of Tast genes and the presence of GM6001 impaired larval development at the metamorphic stage, suggesting that Tast gene products play a key role in late development.

Details

Title
The role of metalloproteases in fertilisation in the ascidian Ciona robusta
Author
Nakazawa Shiori 1   VIAFID ORCID Logo  ; Maki, Shirae-Kurabayashi 2 ; Sawada Hitoshi 2 

 Nagoya University, Sugashima Marine Biological Laboratory, Graduate School of Science, Toba, Japan (GRID:grid.27476.30) (ISNI:0000 0001 0943 978X); Hitachi, Ltd., Research & Development Group, Hatoyama, Hiki, Japan (GRID:grid.417547.4) (ISNI:0000 0004 1763 9564) 
 Nagoya University, Sugashima Marine Biological Laboratory, Graduate School of Science, Toba, Japan (GRID:grid.27476.30) (ISNI:0000 0001 0943 978X) 
Publication year
2019
Publication date
Jan 2019
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2173761049
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.