Home > Research > Publications & Outputs > Modulation of a cytoskeletal calpain-like prote...

Electronic data

  • J Cell Biol-2014-Hayes-377-84

    Rights statement: This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

    Final published version, 1.84 MB, PDF document

    Available under license: CC BY-NC-SA

Links

Text available via DOI:

View graph of relations

Modulation of a cytoskeletal calpain-like protein induces major transitions in trypanosome morphology

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published
  • Polly Hayes
  • Vladimir Varga
  • Sofia Olego-Fernandez
  • Jack Sunter
  • Michael Ginger
  • Keith Gull
Close
<mark>Journal publication date</mark>4/08/2014
<mark>Journal</mark>Journal of Cell Biology
Issue number3
Volume206
Number of pages8
Pages (from-to)377-384
Publication StatusPublished
<mark>Original language</mark>English

Abstract

Individual eukaryotic microbes, such as the kinetoplastid parasite Trypanosoma brucei, have a defined size, shape, and form yet transition through life cycle stages, each having a distinct morphology. In questioning the structural processes involved in these transitions, we have identified a large calpain-like protein that contains numerous GM6 repeats (ClpGM6) involved in determining T. brucei cell shape, size, and form. ClpGM6 is a cytoskeletal protein located within the flagellum along the flagellar attachment zone (FAZ). Depletion of ClpGM6 in trypomastigote forms produces cells with long free flagella and a shorter FAZ, accompanied by repositioning of the basal body, the kinetoplast, Golgi, and flagellar pocket, reflecting an epimastigote-like morphology. Hence, major changes in microbial cell form can be achieved by simple modulation of one or a few proteins via coordinated association and positioning of membrane and cytoskeletal components.

Bibliographic note

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).