Abstract

Separase is a protease that promotes chromosome segregation at anaphase by cleaving cohesin. Several non-proteolytic functions of separase have been identified in other organisms. We created a transgenic C. elegans line that expresses protease-dead separase in embryos to further characterize separase function. We find that expression of protease-dead separase is dominant-negative in C. elegans embryos, not previously reported in other systems. The C. elegans embryo is an ideal system to study developmental processes in a genetically tractable system. However, a major limitation is the lack of an inducible gene expression system for the embryo. We have developed two methods that allow for the propagation of lines carrying dominant-negative transgenes and have applied them to characterize expression of protease-dead separase in embryos. Using these methods, we show that protease-dead separase causes embryo lethality, and that protease-dead separase cannot rescue separase mutants. These data suggest that protease-dead separase interferes with endogenous separase function, possibly by binding substrates and protecting them from cleavage.

Highlights

  • Separase is a cysteine protease with multiple roles during cell division

  • We created a transgenic worm line expressing protease-dead separase fused to GFP (SEP-1PD::GFP) using standard methods to characterize its expression in C. elegans embryos [17]

  • We employed the methods described in this manuscript to examine the consequence of SEP-1PD expression in the C. elegans embryo

Read more

Summary

Introduction

Separase is a cysteine protease with multiple roles during cell division. In a number of these roles the protease activity of separase is required, including cohesin cleavage at the onset of anaphase [1,2,3,4], DNA repair [5], resolution of chiasmata in mouse oocytes [6], mitotic spindle elongation [7], and centriole duplication [8,9,10]. Additional non-proteolytic functions of separase have been identified, including anaphase exit [11] and Cdc early anaphase release (FEAR) pathway activation [12,13], and polar body extrusion in mouse oocytes [6]. These studies examined protease-dead separase in separase mutant cells and concluded that separase can promote signaling events independent of its protease activity. We created a transgenic worm line expressing protease-dead separase fused to GFP (SEP-1PD::GFP) using standard methods to characterize its expression in C. elegans embryos [17]. We methodologically characterize the usefulness of gfp RNAi as a way to propagate toxic transgenes in the C. elegans embryo

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call