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Fusome topology and inheritance during insect gametogenesis
From insects to mammals, oocytes and sperm develop within germline cysts comprising cells connected by intercellular bridges (ICBs). In numerous insects, formation of the cyst is accompanied by growth of the fusome—a membranous organelle that permeates the cyst. Fusome composition and function are b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949678/ https://www.ncbi.nlm.nih.gov/pubmed/36821548 http://dx.doi.org/10.1371/journal.pcbi.1010875 |
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author | Diegmiller, Rocky Imran Alsous, Jasmin Li, Duojia Yamashita, Yukiko M. Shvartsman, Stanislav Y. |
author_facet | Diegmiller, Rocky Imran Alsous, Jasmin Li, Duojia Yamashita, Yukiko M. Shvartsman, Stanislav Y. |
author_sort | Diegmiller, Rocky |
collection | PubMed |
description | From insects to mammals, oocytes and sperm develop within germline cysts comprising cells connected by intercellular bridges (ICBs). In numerous insects, formation of the cyst is accompanied by growth of the fusome—a membranous organelle that permeates the cyst. Fusome composition and function are best understood in Drosophila melanogaster: during oogenesis, the fusome dictates cyst topology and size and facilitates oocyte selection, while during spermatogenesis, the fusome synchronizes the cyst’s response to DNA damage. Despite its distinct and sex-specific roles during insect gametogenesis, elucidating fusome growth and inheritance in females and its structure and connectivity in males has remained challenging. Here, we take advantage of advances in three-dimensional (3D) confocal microscopy and computational image processing tools to reconstruct the topology, growth, and distribution of the fusome in both sexes. In females, our experimental findings inform a theoretical model for fusome assembly and inheritance and suggest that oocyte selection proceeds through an ‘equivalency with a bias’ mechanism. In males, we find that cell divisions can deviate from the maximally branched pattern observed in females, leading to greater topological variability. Our work consolidates existing disjointed experimental observations and contributes a readily generalizable computational approach for quantitative studies of gametogenesis within and across species. |
format | Online Article Text |
id | pubmed-9949678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99496782023-02-24 Fusome topology and inheritance during insect gametogenesis Diegmiller, Rocky Imran Alsous, Jasmin Li, Duojia Yamashita, Yukiko M. Shvartsman, Stanislav Y. PLoS Comput Biol Research Article From insects to mammals, oocytes and sperm develop within germline cysts comprising cells connected by intercellular bridges (ICBs). In numerous insects, formation of the cyst is accompanied by growth of the fusome—a membranous organelle that permeates the cyst. Fusome composition and function are best understood in Drosophila melanogaster: during oogenesis, the fusome dictates cyst topology and size and facilitates oocyte selection, while during spermatogenesis, the fusome synchronizes the cyst’s response to DNA damage. Despite its distinct and sex-specific roles during insect gametogenesis, elucidating fusome growth and inheritance in females and its structure and connectivity in males has remained challenging. Here, we take advantage of advances in three-dimensional (3D) confocal microscopy and computational image processing tools to reconstruct the topology, growth, and distribution of the fusome in both sexes. In females, our experimental findings inform a theoretical model for fusome assembly and inheritance and suggest that oocyte selection proceeds through an ‘equivalency with a bias’ mechanism. In males, we find that cell divisions can deviate from the maximally branched pattern observed in females, leading to greater topological variability. Our work consolidates existing disjointed experimental observations and contributes a readily generalizable computational approach for quantitative studies of gametogenesis within and across species. Public Library of Science 2023-02-23 /pmc/articles/PMC9949678/ /pubmed/36821548 http://dx.doi.org/10.1371/journal.pcbi.1010875 Text en © 2023 Diegmiller et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Diegmiller, Rocky Imran Alsous, Jasmin Li, Duojia Yamashita, Yukiko M. Shvartsman, Stanislav Y. Fusome topology and inheritance during insect gametogenesis |
title | Fusome topology and inheritance during insect gametogenesis |
title_full | Fusome topology and inheritance during insect gametogenesis |
title_fullStr | Fusome topology and inheritance during insect gametogenesis |
title_full_unstemmed | Fusome topology and inheritance during insect gametogenesis |
title_short | Fusome topology and inheritance during insect gametogenesis |
title_sort | fusome topology and inheritance during insect gametogenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949678/ https://www.ncbi.nlm.nih.gov/pubmed/36821548 http://dx.doi.org/10.1371/journal.pcbi.1010875 |
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