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The role of acroblast formation during Drosophila spermatogenesis

Protein recycling is important for maintaining homeostasis of the Golgi and its cisternae. The Vps54 (Scat) protein, a subunit of the GARP tethering complex, is a central factor in retrograde transport to the trans-Golgi. We found the scat(1) mutant to be male sterile in Drosophila with individualiz...

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Autores principales: Fári, Karolina, Takács, Sándor, Ungár, Dániel, Sinka, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004609/
https://www.ncbi.nlm.nih.gov/pubmed/27481842
http://dx.doi.org/10.1242/bio.018275
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author Fári, Karolina
Takács, Sándor
Ungár, Dániel
Sinka, Rita
author_facet Fári, Karolina
Takács, Sándor
Ungár, Dániel
Sinka, Rita
author_sort Fári, Karolina
collection PubMed
description Protein recycling is important for maintaining homeostasis of the Golgi and its cisternae. The Vps54 (Scat) protein, a subunit of the GARP tethering complex, is a central factor in retrograde transport to the trans-Golgi. We found the scat(1) mutant to be male sterile in Drosophila with individualization problems occurring during spermatogenesis. Another typically observed phenotype was the abnormal nuclear structure in elongated mutant cysts. When examining the structure and function of the Golgi, a failure in acrosome formation and endosome-Golgi vesicular transport were found in the scat(1) mutant. This acrosome formation defect was due to a fault in the trans-Golgi side of the acroblast ribbon. When testing a mutation in a second retrograde transport protein, Fws, a subunit of the conserved oligomeric Golgi (COG) tethering complex, the acroblast structure, was again disrupted. fws(P) caused a similar, albeit milder, acrosome and sperm individualization phenotype as the scat(1) mutant. In the case of fws(P) the cis side of the acroblast ribbon was dispersed, in-line with the intra-Golgi retrograde function of COG. Our results highlight the importance of an intact acroblast for acrosome formation, nuclear elongation and therefore sperm maturation. Moreover, these results suggest the importance of retrograde tethering complexes in the formation of a functional Golgi ribbon.
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spelling pubmed-50046092016-09-08 The role of acroblast formation during Drosophila spermatogenesis Fári, Karolina Takács, Sándor Ungár, Dániel Sinka, Rita Biol Open Research Article Protein recycling is important for maintaining homeostasis of the Golgi and its cisternae. The Vps54 (Scat) protein, a subunit of the GARP tethering complex, is a central factor in retrograde transport to the trans-Golgi. We found the scat(1) mutant to be male sterile in Drosophila with individualization problems occurring during spermatogenesis. Another typically observed phenotype was the abnormal nuclear structure in elongated mutant cysts. When examining the structure and function of the Golgi, a failure in acrosome formation and endosome-Golgi vesicular transport were found in the scat(1) mutant. This acrosome formation defect was due to a fault in the trans-Golgi side of the acroblast ribbon. When testing a mutation in a second retrograde transport protein, Fws, a subunit of the conserved oligomeric Golgi (COG) tethering complex, the acroblast structure, was again disrupted. fws(P) caused a similar, albeit milder, acrosome and sperm individualization phenotype as the scat(1) mutant. In the case of fws(P) the cis side of the acroblast ribbon was dispersed, in-line with the intra-Golgi retrograde function of COG. Our results highlight the importance of an intact acroblast for acrosome formation, nuclear elongation and therefore sperm maturation. Moreover, these results suggest the importance of retrograde tethering complexes in the formation of a functional Golgi ribbon. The Company of Biologists Ltd 2016-08-01 /pmc/articles/PMC5004609/ /pubmed/27481842 http://dx.doi.org/10.1242/bio.018275 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Fári, Karolina
Takács, Sándor
Ungár, Dániel
Sinka, Rita
The role of acroblast formation during Drosophila spermatogenesis
title The role of acroblast formation during Drosophila spermatogenesis
title_full The role of acroblast formation during Drosophila spermatogenesis
title_fullStr The role of acroblast formation during Drosophila spermatogenesis
title_full_unstemmed The role of acroblast formation during Drosophila spermatogenesis
title_short The role of acroblast formation during Drosophila spermatogenesis
title_sort role of acroblast formation during drosophila spermatogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004609/
https://www.ncbi.nlm.nih.gov/pubmed/27481842
http://dx.doi.org/10.1242/bio.018275
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