Distinct roles of two myosins in C. elegans spermatid differentiation.

During spermatogenesis, interconnected haploid spermatids segregate undesired cellular contents into residual bodies (RBs) before detaching from RBs. It is unclear how this differentiation process is controlled to produce individual spermatids or motile spermatozoa. Here, we developed a live imaging...

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Main Authors: Junyan Hu, Shiya Cheng, Haibin Wang, Xin Li, Sun Liu, Mengmeng Wu, Yubing Liu, Xiaochen Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-04-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.3000211
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spelling doaj-7c60f06e0b444312aa5dcdbd595fa17f2021-07-02T17:07:44ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852019-04-01174e300021110.1371/journal.pbio.3000211Distinct roles of two myosins in C. elegans spermatid differentiation.Junyan HuShiya ChengHaibin WangXin LiSun LiuMengmeng WuYubing LiuXiaochen WangDuring spermatogenesis, interconnected haploid spermatids segregate undesired cellular contents into residual bodies (RBs) before detaching from RBs. It is unclear how this differentiation process is controlled to produce individual spermatids or motile spermatozoa. Here, we developed a live imaging system to visualize and investigate this process in C. elegans. We found that non-muscle myosin 2 (NMY-2)/myosin II drives incomplete cytokinesis to generate connected haploid spermatids, which are then polarized to segregate undesired cellular contents into RBs under the control of myosin II and myosin VI. NMY-2/myosin II extends from the pseudo-cleavage furrow formed between two haploid spermatids to the spermatid poles, thus promoting RB expansion. In the meantime, defective spermatogenesis 15 (SPE-15)/myosin VI migrates from spermatids towards the expanding RB to promote spermatid budding. Loss of myosin II or myosin VI causes distinct cytoplasm segregation defects, while loss of both myosins completely blocks RB formation. We found that the final separation of spermatids from RBs is achieved through myosin VI-mediated cytokinesis, while myosin II is dispensable at this step. SPE-15/myosin VI and F-actin form a detergent-resistant actomyosin VI ring that undergoes continuous contraction to promote membrane constriction between spermatid and RB. We further identified that RGS-GAIP-interacting protein C terminus (GIPC)-1 and GIPC-2 cooperate with myosin VI to regulate contractile ring formation and spermatid release. Our study reveals distinct roles of myosin II and myosin VI in spermatid differentiation and uncovers a novel myosin VI-mediated cytokinesis process that controls spermatid release.https://doi.org/10.1371/journal.pbio.3000211
collection DOAJ
language English
format Article
sources DOAJ
author Junyan Hu
Shiya Cheng
Haibin Wang
Xin Li
Sun Liu
Mengmeng Wu
Yubing Liu
Xiaochen Wang
spellingShingle Junyan Hu
Shiya Cheng
Haibin Wang
Xin Li
Sun Liu
Mengmeng Wu
Yubing Liu
Xiaochen Wang
Distinct roles of two myosins in C. elegans spermatid differentiation.
PLoS Biology
author_facet Junyan Hu
Shiya Cheng
Haibin Wang
Xin Li
Sun Liu
Mengmeng Wu
Yubing Liu
Xiaochen Wang
author_sort Junyan Hu
title Distinct roles of two myosins in C. elegans spermatid differentiation.
title_short Distinct roles of two myosins in C. elegans spermatid differentiation.
title_full Distinct roles of two myosins in C. elegans spermatid differentiation.
title_fullStr Distinct roles of two myosins in C. elegans spermatid differentiation.
title_full_unstemmed Distinct roles of two myosins in C. elegans spermatid differentiation.
title_sort distinct roles of two myosins in c. elegans spermatid differentiation.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2019-04-01
description During spermatogenesis, interconnected haploid spermatids segregate undesired cellular contents into residual bodies (RBs) before detaching from RBs. It is unclear how this differentiation process is controlled to produce individual spermatids or motile spermatozoa. Here, we developed a live imaging system to visualize and investigate this process in C. elegans. We found that non-muscle myosin 2 (NMY-2)/myosin II drives incomplete cytokinesis to generate connected haploid spermatids, which are then polarized to segregate undesired cellular contents into RBs under the control of myosin II and myosin VI. NMY-2/myosin II extends from the pseudo-cleavage furrow formed between two haploid spermatids to the spermatid poles, thus promoting RB expansion. In the meantime, defective spermatogenesis 15 (SPE-15)/myosin VI migrates from spermatids towards the expanding RB to promote spermatid budding. Loss of myosin II or myosin VI causes distinct cytoplasm segregation defects, while loss of both myosins completely blocks RB formation. We found that the final separation of spermatids from RBs is achieved through myosin VI-mediated cytokinesis, while myosin II is dispensable at this step. SPE-15/myosin VI and F-actin form a detergent-resistant actomyosin VI ring that undergoes continuous contraction to promote membrane constriction between spermatid and RB. We further identified that RGS-GAIP-interacting protein C terminus (GIPC)-1 and GIPC-2 cooperate with myosin VI to regulate contractile ring formation and spermatid release. Our study reveals distinct roles of myosin II and myosin VI in spermatid differentiation and uncovers a novel myosin VI-mediated cytokinesis process that controls spermatid release.
url https://doi.org/10.1371/journal.pbio.3000211
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