Combinatorial and antagonistic effects of tubulin glutamylation and glycylation on katanin microtubule severing.

ABSTRACT: Microtubules have spatiotemporally complex posttranslational modification patterns. How cells interpret this tubulin modification code is largely unknown. We show that C. elegans katanin, a microtubule severing AAA ATPase mutated in microcephaly and critical for cell division, axonal elongation, and cilia biogenesis, responds precisely, differentially, and combinatorially to three chemically distinct tubulin modifications-glycylation, glutamylation, and tyrosination-but is insensitive to acetylation. Glutamylation and glycylation are antagonistic rheostats with glycylation protecting microtubules from severing. Katanin exhibits graded and divergent responses to glutamylation on the α- and β-tubulin tails, and these act combinatorially. The katanin hexamer central pore constrains the polygl

SUBMITTER: Szczesna E 

PROVIDER: S-EPMC9665884 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature