Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons

Pruning, whereby neurons eliminate their excess neurites, is central for the maturation of the nervous system. In Drosophila, sensory neurons, ddaCs, selectively prune their larval dendrites without affecting their axons during metamorphosis. However, it is unknown whether the secretory pathway play...

Full description

Saved in:
Bibliographic Details
Main Authors: Wang, Yan, Zhang, Heng, Shi, Meng, Liou, Yih-Cherng, Lu, Lei, Yu, Fengwei
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2017
Subjects:
Online Access:https://hdl.handle.net/10356/81485
http://hdl.handle.net/10220/43488
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-81485
record_format dspace
spelling sg-ntu-dr.10356-814852023-02-28T16:58:44Z Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons Wang, Yan Zhang, Heng Shi, Meng Liou, Yih-Cherng Lu, Lei Yu, Fengwei School of Biological Sciences Pruning Dendrite Pruning, whereby neurons eliminate their excess neurites, is central for the maturation of the nervous system. In Drosophila, sensory neurons, ddaCs, selectively prune their larval dendrites without affecting their axons during metamorphosis. However, it is unknown whether the secretory pathway plays a role in dendrite pruning. Here, we show that the small GTPase Arf1, an important regulator of the secretory pathway, is specifically required for dendrite pruning of ddaC/D/E sensory neurons but dispensable for apoptosis of ddaF neurons. Analyses of the GTP- and GDP-locked forms of Arf1 indicate that the cycling of Arf1 between GDP-bound and GTP-bound forms is essential for dendrite pruning. We further identified Sec71 as a guanine nucleotide exchange factor for Arf1 that preferentially interacts with its GDP-bound form. Like Arf1, Sec71 is also important for dendrite pruning, but not for apoptosis, of sensory neurons. Arf1 and Sec71 are interdependent for their localizations on Golgi. Finally, we show that the Sec71/Arf1-mediated trafficking process is a prerequisite for Rab5-dependent endocytosis to facilitate endocytosis and degradation of the cell-adhesion molecule Neuroglian (Nrg). MOE (Min. of Education, S’pore) Published version 2017-07-28T02:52:54Z 2019-12-06T14:32:01Z 2017-07-28T02:52:54Z 2019-12-06T14:32:01Z 2017 Journal Article Wang, Y., Zhang, H., Shi, M., Liou, Y.-C., Lu, L., & Yu, F. (2017). Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons. Development, 144, 1851-1862. 0950-1991 https://hdl.handle.net/10356/81485 http://hdl.handle.net/10220/43488 10.1242/dev.146175 en Development © 2017 The Author(s) (published by The Company of Biologists Ltd). This paper was published in Development and is made available as an electronic reprint (preprint) with permission of The Author(s) (published by The Company of Biologists Ltd). The published version is available at: [http://dx.doi.org/10.1242/dev.146175]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. 12 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Pruning
Dendrite
spellingShingle Pruning
Dendrite
Wang, Yan
Zhang, Heng
Shi, Meng
Liou, Yih-Cherng
Lu, Lei
Yu, Fengwei
Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons
description Pruning, whereby neurons eliminate their excess neurites, is central for the maturation of the nervous system. In Drosophila, sensory neurons, ddaCs, selectively prune their larval dendrites without affecting their axons during metamorphosis. However, it is unknown whether the secretory pathway plays a role in dendrite pruning. Here, we show that the small GTPase Arf1, an important regulator of the secretory pathway, is specifically required for dendrite pruning of ddaC/D/E sensory neurons but dispensable for apoptosis of ddaF neurons. Analyses of the GTP- and GDP-locked forms of Arf1 indicate that the cycling of Arf1 between GDP-bound and GTP-bound forms is essential for dendrite pruning. We further identified Sec71 as a guanine nucleotide exchange factor for Arf1 that preferentially interacts with its GDP-bound form. Like Arf1, Sec71 is also important for dendrite pruning, but not for apoptosis, of sensory neurons. Arf1 and Sec71 are interdependent for their localizations on Golgi. Finally, we show that the Sec71/Arf1-mediated trafficking process is a prerequisite for Rab5-dependent endocytosis to facilitate endocytosis and degradation of the cell-adhesion molecule Neuroglian (Nrg).
author2 School of Biological Sciences
author_facet School of Biological Sciences
Wang, Yan
Zhang, Heng
Shi, Meng
Liou, Yih-Cherng
Lu, Lei
Yu, Fengwei
format Article
author Wang, Yan
Zhang, Heng
Shi, Meng
Liou, Yih-Cherng
Lu, Lei
Yu, Fengwei
author_sort Wang, Yan
title Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons
title_short Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons
title_full Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons
title_fullStr Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons
title_full_unstemmed Sec71 functions as a GEF for the small GTPase Arf1 to govern dendrite pruning of Drosophila sensory neurons
title_sort sec71 functions as a gef for the small gtpase arf1 to govern dendrite pruning of drosophila sensory neurons
publishDate 2017
url https://hdl.handle.net/10356/81485
http://hdl.handle.net/10220/43488
_version_ 1759857991836762112