Protease-dead separase is dominant negative in the C. elegans embryo.

PLoS One

Department of Biochemistry, Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee, United States of America.

Published: December 2015

AI Article Synopsis

  • Separase is a protease important for chromosome separation during cell division, but it also has non-proteolytic roles in other organisms.
  • Researchers created a transgenic line of the roundworm C. elegans that expresses a non-functional version of separase to study its effects on embryo development.
  • The results showed that this non-functional separase leads to embryo death and does not help separase mutants, indicating it disrupts normal separase activity by potentially blocking its interaction with substrates.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171520PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0108188PLOS

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