Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.

Mitotic divisions depend on the timely assembly and proper orientation of the mitotic spindle. Malfunctioning of these processes can considerably delay mitosis, thereby compromising tissue growth and homeostasis, and leading to chromosomal instability. Loss of functional Mms19 drastically affects th...

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Main Authors: Rohan Chippalkatti, Boris Egger, Beat Suter
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-11-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008913
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spelling doaj-be61fbae61cf42b7b8f89c0691c5ad602021-04-21T14:34:25ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042020-11-011611e100891310.1371/journal.pgen.1008913Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.Rohan ChippalkattiBoris EggerBeat SuterMitotic divisions depend on the timely assembly and proper orientation of the mitotic spindle. Malfunctioning of these processes can considerably delay mitosis, thereby compromising tissue growth and homeostasis, and leading to chromosomal instability. Loss of functional Mms19 drastically affects the growth and development of mitotic tissues in Drosophila larvae and we now demonstrate that Mms19 is an important factor that promotes spindle and astral microtubule (MT) growth, and MT stability and bundling. Mms19 function is needed for the coordination of mitotic events and for the rapid progression through mitosis that is characteristic of neural stem cells. Surprisingly, Mms19 performs its mitotic activities through two different pathways. By stimulating the mitotic kinase cascade, it triggers the localization of the MT regulatory complex TACC/Msps (Transforming Acidic Coiled Coil/Minispindles, the homolog of human ch-TOG) to the centrosome. This activity of Mms19 can be rescued by stimulating the mitotic kinase cascade. However, other aspects of the Mms19 phenotypes cannot be rescued in this way, pointing to an additional mechanism of Mms19 action. We provide evidence that Mms19 binds directly to MTs and that this stimulates MT stability and bundling.https://doi.org/10.1371/journal.pgen.1008913
collection DOAJ
language English
format Article
sources DOAJ
author Rohan Chippalkatti
Boris Egger
Beat Suter
spellingShingle Rohan Chippalkatti
Boris Egger
Beat Suter
Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.
PLoS Genetics
author_facet Rohan Chippalkatti
Boris Egger
Beat Suter
author_sort Rohan Chippalkatti
title Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.
title_short Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.
title_full Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.
title_fullStr Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.
title_full_unstemmed Mms19 promotes spindle microtubule assembly in Drosophila neural stem cells.
title_sort mms19 promotes spindle microtubule assembly in drosophila neural stem cells.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2020-11-01
description Mitotic divisions depend on the timely assembly and proper orientation of the mitotic spindle. Malfunctioning of these processes can considerably delay mitosis, thereby compromising tissue growth and homeostasis, and leading to chromosomal instability. Loss of functional Mms19 drastically affects the growth and development of mitotic tissues in Drosophila larvae and we now demonstrate that Mms19 is an important factor that promotes spindle and astral microtubule (MT) growth, and MT stability and bundling. Mms19 function is needed for the coordination of mitotic events and for the rapid progression through mitosis that is characteristic of neural stem cells. Surprisingly, Mms19 performs its mitotic activities through two different pathways. By stimulating the mitotic kinase cascade, it triggers the localization of the MT regulatory complex TACC/Msps (Transforming Acidic Coiled Coil/Minispindles, the homolog of human ch-TOG) to the centrosome. This activity of Mms19 can be rescued by stimulating the mitotic kinase cascade. However, other aspects of the Mms19 phenotypes cannot be rescued in this way, pointing to an additional mechanism of Mms19 action. We provide evidence that Mms19 binds directly to MTs and that this stimulates MT stability and bundling.
url https://doi.org/10.1371/journal.pgen.1008913
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