Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.

During zebrafish development, a gradient of stromal-derived factor 1a (Sdf1a) provides the directional cue that guides the migration of the primordial germ cells (PGCs) to the gonadal tissue. Here we describe a method to produce large numbers of infertile fish by inducing ubiquitous expression of Sd...

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Main Authors: Ten-Tsao Wong, Paul Collodi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3694954?pdf=render
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spelling doaj-f8e8ee5ecefd44ddbf6bc26d60bf59442020-11-25T01:03:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6845510.1371/journal.pone.0068455Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.Ten-Tsao WongPaul CollodiDuring zebrafish development, a gradient of stromal-derived factor 1a (Sdf1a) provides the directional cue that guides the migration of the primordial germ cells (PGCs) to the gonadal tissue. Here we describe a method to produce large numbers of infertile fish by inducing ubiquitous expression of Sdf1a in zebrafish embryos resulting in disruption of the normal PGC migration pattern. A transgenic line of zebrafish, Tg(hsp70:sdf1a-nanos3, EGFP), was generated that expresses Sdf1a under the control of the heat-shock protein 70 (hsp70) promoter and nanos3 3?UTR. To better visualize the PGCs, the Tg(hsp70:sdf1a-nanos3, EGFP) fish were crossed with another transgenic line, Tg(kop:DsRed-nanos3), that expresses DsRed driven by the PGC-specific kop promoter. Heat treatment of the transgenic embryos caused an induction of Sdf1a expression throughout the embryo resulting in the disruption of their normal migration. Optimal embryo survival and disruption of PGC migration was achieved when transgenic embryos at the 4- to 8-cell stage were incubated at 34.5°C for 18 hours. Under these conditions, disruption of PGC migration was observed in 100% of the embryos. Sixty-four adult fish were developed from three separate batches of heat-treated embryos and all were found to be infertile males. When each male was paired with a wild-type female, only unfertilized eggs were produced and histological examination revealed that each of the adult male fish possessed severely under-developed gonads that lacked gametes. The results demonstrate that inducible Sdf1a expression is an efficient and reliable strategy to produce infertile fish. This approach makes it convenient to generate large numbers of infertile adult fish while also providing the capability to maintain a fertile brood stock.http://europepmc.org/articles/PMC3694954?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ten-Tsao Wong
Paul Collodi
spellingShingle Ten-Tsao Wong
Paul Collodi
Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.
PLoS ONE
author_facet Ten-Tsao Wong
Paul Collodi
author_sort Ten-Tsao Wong
title Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.
title_short Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.
title_full Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.
title_fullStr Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.
title_full_unstemmed Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration.
title_sort inducible sterilization of zebrafish by disruption of primordial germ cell migration.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description During zebrafish development, a gradient of stromal-derived factor 1a (Sdf1a) provides the directional cue that guides the migration of the primordial germ cells (PGCs) to the gonadal tissue. Here we describe a method to produce large numbers of infertile fish by inducing ubiquitous expression of Sdf1a in zebrafish embryos resulting in disruption of the normal PGC migration pattern. A transgenic line of zebrafish, Tg(hsp70:sdf1a-nanos3, EGFP), was generated that expresses Sdf1a under the control of the heat-shock protein 70 (hsp70) promoter and nanos3 3?UTR. To better visualize the PGCs, the Tg(hsp70:sdf1a-nanos3, EGFP) fish were crossed with another transgenic line, Tg(kop:DsRed-nanos3), that expresses DsRed driven by the PGC-specific kop promoter. Heat treatment of the transgenic embryos caused an induction of Sdf1a expression throughout the embryo resulting in the disruption of their normal migration. Optimal embryo survival and disruption of PGC migration was achieved when transgenic embryos at the 4- to 8-cell stage were incubated at 34.5°C for 18 hours. Under these conditions, disruption of PGC migration was observed in 100% of the embryos. Sixty-four adult fish were developed from three separate batches of heat-treated embryos and all were found to be infertile males. When each male was paired with a wild-type female, only unfertilized eggs were produced and histological examination revealed that each of the adult male fish possessed severely under-developed gonads that lacked gametes. The results demonstrate that inducible Sdf1a expression is an efficient and reliable strategy to produce infertile fish. This approach makes it convenient to generate large numbers of infertile adult fish while also providing the capability to maintain a fertile brood stock.
url http://europepmc.org/articles/PMC3694954?pdf=render
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