Correlation Engine 2.0
Clear Search sequence regions

Sizes of these terms reflect their relevance to your search.

Tubulin polyglutamylation, catalysed by members of the tubulin tyrosine ligase-like (TTLL) protein family, is an evolutionarily highly conserved mechanism involved in the regulation of microtubule dynamics and function in eukaryotes. In the protozoan parasite Trypanosoma brucei, the microtubule cytoskeleton is essential for cell motility and maintaining cell shape. In a previous study, we showed that T. brucei TTLL6A and TTLL12B are required to regulate microtubule dynamics at the posterior cell pole. Here, using gene deletion, we show that the polyglutamylase TTLL1 is essential for the integrity of the highly organised microtubule structure at the cell pole, with a phenotype distinct from that observed in TTLL6A- and TTLL12B-depleted cells. Reduced polyglutamylation in TTLL1-deficient cells also leads to increased levels in tubulin tyrosination, providing new evidence for an interplay between the tubulin tyrosination and detyrosination cycle and polyglutamylation. We also show that TTLL1 acts differentially on specific microtubule doublets of the flagellar axoneme, although the absence of TTLL1 appears to have no measurable effect on cell motility. © 2024. Published by The Company of Biologists Ltd.


Jana Jentzsch, Hannes Wunderlich, Marinus Thein, Julia Bechthold, Lucas Brehm, Sebastian W Krauss, Matthias Weiss, Klaus Ersfeld. Microtubule polyglutamylation is an essential regulator of cytoskeletal integrity in Trypanosoma brucei. Journal of cell science. 2024 Feb 01;137(3)

Expand section icon Mesh Tags

Expand section icon Substances

PMID: 38205672

View Full Text