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A spindle-independent cleavage pathway controls germ cell formation in Drosophila

The primordial germ cells (PGCs) are the first cells to form during Drosophila melanogaster embryogenesis. While the process of somatic cell formation has been studied in detail, the mechanics of PGC formation are poorly understood. Here, using 4D multi-photon imaging combined with genetic and pharm...

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Detalles Bibliográficos
Autores principales: Cinalli, Ryan M., Lehmann, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818562/
https://www.ncbi.nlm.nih.gov/pubmed/23728423
http://dx.doi.org/10.1038/ncb2761
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author Cinalli, Ryan M.
Lehmann, Ruth
author_facet Cinalli, Ryan M.
Lehmann, Ruth
author_sort Cinalli, Ryan M.
collection PubMed
description The primordial germ cells (PGCs) are the first cells to form during Drosophila melanogaster embryogenesis. While the process of somatic cell formation has been studied in detail, the mechanics of PGC formation are poorly understood. Here, using 4D multi-photon imaging combined with genetic and pharmacological manipulations, we find that PGC formation requires an anaphase spindle-independent cleavage pathway. In addition to utilizing core regulators of cleavage, including the small GTPase RhoA (Drosophila Rho) and the Rho associated kinase, ROCK (Drosophila Rok), we show that this pathway requires Germ cell-less (Gcl), a conserved BTB-domain protein not previously implicated in cleavage mechanics. This alternate form of cell formation suggests that organisms have evolved multiple molecular strategies for regulating the cytoskeleton during cleavage.
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spelling pubmed-38185622014-01-01 A spindle-independent cleavage pathway controls germ cell formation in Drosophila Cinalli, Ryan M. Lehmann, Ruth Nat Cell Biol Article The primordial germ cells (PGCs) are the first cells to form during Drosophila melanogaster embryogenesis. While the process of somatic cell formation has been studied in detail, the mechanics of PGC formation are poorly understood. Here, using 4D multi-photon imaging combined with genetic and pharmacological manipulations, we find that PGC formation requires an anaphase spindle-independent cleavage pathway. In addition to utilizing core regulators of cleavage, including the small GTPase RhoA (Drosophila Rho) and the Rho associated kinase, ROCK (Drosophila Rok), we show that this pathway requires Germ cell-less (Gcl), a conserved BTB-domain protein not previously implicated in cleavage mechanics. This alternate form of cell formation suggests that organisms have evolved multiple molecular strategies for regulating the cytoskeleton during cleavage. 2013-06-02 2013-07 /pmc/articles/PMC3818562/ /pubmed/23728423 http://dx.doi.org/10.1038/ncb2761 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Cinalli, Ryan M.
Lehmann, Ruth
A spindle-independent cleavage pathway controls germ cell formation in Drosophila
title A spindle-independent cleavage pathway controls germ cell formation in Drosophila
title_full A spindle-independent cleavage pathway controls germ cell formation in Drosophila
title_fullStr A spindle-independent cleavage pathway controls germ cell formation in Drosophila
title_full_unstemmed A spindle-independent cleavage pathway controls germ cell formation in Drosophila
title_short A spindle-independent cleavage pathway controls germ cell formation in Drosophila
title_sort spindle-independent cleavage pathway controls germ cell formation in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818562/
https://www.ncbi.nlm.nih.gov/pubmed/23728423
http://dx.doi.org/10.1038/ncb2761
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