TY - JOUR
T1 - Patronin-mediated minus end growth is required for dendritic microtubule polarity
AU - Feng, Chengye
AU - Thyagarajan, Pankajam
AU - Shorey, Matthew
AU - Seebold, Dylan Y.
AU - Weiner, Alexis T.
AU - Albertson, Richard M.
AU - Rao, Kavitha S.
AU - Sagasti, Alvaro
AU - Goetschius, Daniel J.
AU - Rolls, Melissa M.
N1 - Funding Information:
Funding for this work came from the National Institutes of Health grants R01GM085115 (M.M. Rolls), R21NS066216 (M.M. Rolls), and R21NS090027 (A. Sagasti and M.M. Rolls). The authors declare no competing financial interests.
Publisher Copyright:
© 2019 Feng et al. 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 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
PY - 2019
Y1 - 2019
N2 - Microtubule minus ends are thought to be stable in cells. Surprisingly, in Drosophila and zebrafish neurons, we observed persistent minus end growth, with runs lasting over 10 min. In Drosophila, extended minus end growth depended on Patronin, and Patronin reduction disrupted dendritic minus-end-out polarity. In fly dendrites, microtubule nucleation sites localize at dendrite branch points. Therefore, we hypothesized minus end growth might be particularly important beyond branch points. Distal dendrites have mixed polarity, and reduction of Patronin lowered the number of minus-end-out microtubules. More strikingly, extra Patronin made terminal dendrites almost completely minus-end-out, indicating low Patronin normally limits minus-end-out microtubules. To determine whether minus end growth populated new dendrites with microtubules, we analyzed dendrite development and regeneration. Minus ends extended into growing dendrites in the presence of Patronin. In sum, our data suggest that Patronin facilitates sustained microtubule minus end growth, which is critical for populating dendrites with minus-end-out microtubules.
AB - Microtubule minus ends are thought to be stable in cells. Surprisingly, in Drosophila and zebrafish neurons, we observed persistent minus end growth, with runs lasting over 10 min. In Drosophila, extended minus end growth depended on Patronin, and Patronin reduction disrupted dendritic minus-end-out polarity. In fly dendrites, microtubule nucleation sites localize at dendrite branch points. Therefore, we hypothesized minus end growth might be particularly important beyond branch points. Distal dendrites have mixed polarity, and reduction of Patronin lowered the number of minus-end-out microtubules. More strikingly, extra Patronin made terminal dendrites almost completely minus-end-out, indicating low Patronin normally limits minus-end-out microtubules. To determine whether minus end growth populated new dendrites with microtubules, we analyzed dendrite development and regeneration. Minus ends extended into growing dendrites in the presence of Patronin. In sum, our data suggest that Patronin facilitates sustained microtubule minus end growth, which is critical for populating dendrites with minus-end-out microtubules.
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U2 - 10.1083/jcb.201810155
DO - 10.1083/jcb.201810155
M3 - Article
C2 - 31076454
AN - SCOPUS:85069264098
SN - 0021-9525
VL - 218
SP - 2309
EP - 2328
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 7
ER -