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A dynamic basal complex modulates mammalian sperm movement
Reproductive success depends on efficient sperm movement driven by axonemal dynein-mediated microtubule sliding. Models predict sliding at the base of the tail – the centriole – but such sliding has never been observed. Centrioles are ancient organelles with a conserved architecture; their rigidity...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217517/ https://www.ncbi.nlm.nih.gov/pubmed/34155206 http://dx.doi.org/10.1038/s41467-021-24011-0 |
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author | Khanal, Sushil Leung, Miguel Ricardo Royfman, Abigail Fishman, Emily L. Saltzman, Barbara Bloomfield-Gadêlha, Hermes Zeev-Ben-Mordehai, Tzviya Avidor-Reiss, Tomer |
author_facet | Khanal, Sushil Leung, Miguel Ricardo Royfman, Abigail Fishman, Emily L. Saltzman, Barbara Bloomfield-Gadêlha, Hermes Zeev-Ben-Mordehai, Tzviya Avidor-Reiss, Tomer |
author_sort | Khanal, Sushil |
collection | PubMed |
description | Reproductive success depends on efficient sperm movement driven by axonemal dynein-mediated microtubule sliding. Models predict sliding at the base of the tail – the centriole – but such sliding has never been observed. Centrioles are ancient organelles with a conserved architecture; their rigidity is thought to restrict microtubule sliding. Here, we show that, in mammalian sperm, the atypical distal centriole (DC) and its surrounding atypical pericentriolar matrix form a dynamic basal complex (DBC) that facilitates a cascade of internal sliding deformations, coupling tail beating with asymmetric head kinking. During asymmetric tail beating, the DC’s right side and its surroundings slide ~300 nm rostrally relative to the left side. The deformation throughout the DBC is transmitted to the head-tail junction; thus, the head tilts to the left, generating a kinking motion. These findings suggest that the DBC evolved as a dynamic linker coupling sperm head and tail into a single self-coordinated system. |
format | Online Article Text |
id | pubmed-8217517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82175172021-07-09 A dynamic basal complex modulates mammalian sperm movement Khanal, Sushil Leung, Miguel Ricardo Royfman, Abigail Fishman, Emily L. Saltzman, Barbara Bloomfield-Gadêlha, Hermes Zeev-Ben-Mordehai, Tzviya Avidor-Reiss, Tomer Nat Commun Article Reproductive success depends on efficient sperm movement driven by axonemal dynein-mediated microtubule sliding. Models predict sliding at the base of the tail – the centriole – but such sliding has never been observed. Centrioles are ancient organelles with a conserved architecture; their rigidity is thought to restrict microtubule sliding. Here, we show that, in mammalian sperm, the atypical distal centriole (DC) and its surrounding atypical pericentriolar matrix form a dynamic basal complex (DBC) that facilitates a cascade of internal sliding deformations, coupling tail beating with asymmetric head kinking. During asymmetric tail beating, the DC’s right side and its surroundings slide ~300 nm rostrally relative to the left side. The deformation throughout the DBC is transmitted to the head-tail junction; thus, the head tilts to the left, generating a kinking motion. These findings suggest that the DBC evolved as a dynamic linker coupling sperm head and tail into a single self-coordinated system. Nature Publishing Group UK 2021-06-21 /pmc/articles/PMC8217517/ /pubmed/34155206 http://dx.doi.org/10.1038/s41467-021-24011-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Khanal, Sushil Leung, Miguel Ricardo Royfman, Abigail Fishman, Emily L. Saltzman, Barbara Bloomfield-Gadêlha, Hermes Zeev-Ben-Mordehai, Tzviya Avidor-Reiss, Tomer A dynamic basal complex modulates mammalian sperm movement |
title | A dynamic basal complex modulates mammalian sperm movement |
title_full | A dynamic basal complex modulates mammalian sperm movement |
title_fullStr | A dynamic basal complex modulates mammalian sperm movement |
title_full_unstemmed | A dynamic basal complex modulates mammalian sperm movement |
title_short | A dynamic basal complex modulates mammalian sperm movement |
title_sort | dynamic basal complex modulates mammalian sperm movement |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217517/ https://www.ncbi.nlm.nih.gov/pubmed/34155206 http://dx.doi.org/10.1038/s41467-021-24011-0 |
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