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Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility
The mouse testis-enriched Znf230 gene, which encodes a type of RING finger protein, is present primarily in the nuclei of spermatogonia, the acrosome and the tail of spermatozoa. To investigate the role of Znf230 in spermatogenesis, we generated Znf230-deficient mice by disrupting Znf230 exon-5 and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261971/ https://www.ncbi.nlm.nih.gov/pubmed/25505846 http://dx.doi.org/10.1590/S1415-47572014005000013 |
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author | Liu, Yunqiang Tao, Dachang Lu, Yongjie Yang, Yuan Ma, Yongxin Zhang, Sizhong |
author_facet | Liu, Yunqiang Tao, Dachang Lu, Yongjie Yang, Yuan Ma, Yongxin Zhang, Sizhong |
author_sort | Liu, Yunqiang |
collection | PubMed |
description | The mouse testis-enriched Znf230 gene, which encodes a type of RING finger protein, is present primarily in the nuclei of spermatogonia, the acrosome and the tail of spermatozoa. To investigate the role of Znf230 in spermatogenesis, we generated Znf230-deficient mice by disrupting Znf230 exon-5 and exon-6 using homologous recombination. The homozygous Znf230-knockout (KO) mice did not exhibit Znf230 mRNA expression and Znf230 protein production. Znf230 KO mice exhibited no obvious impairment in body growth or fertility. Male Znf230 KO mice had integral reproductive systems and mature sperm that were regular in number and shape. The developmental stages of male germ cells of Znf230 KO mice were also normal. We further examined variations in the transcriptomes of testicular tissue between Znf230 KO and wild-type mice through microarray analysis. The results showed that the mRNA level of one unclassified transcript 4921513I08Rik was increased and that the mRNA levels of three other transcripts, i.e., 4930448A20Rik, 4931431B13Rik and potassium channel tetramerisation domain containing 14(Kctd14), were reduced more than two-fold in Znf230 KO mice compared with wild-type mice. Using our current examination techniques, these findings suggested that Znf230 deficiency in mice may not affect growth, fertility or spermatogenesis. |
format | Online Article Text |
id | pubmed-4261971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Sociedade Brasileira de Genética |
record_format | MEDLINE/PubMed |
spelling | pubmed-42619712014-12-11 Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility Liu, Yunqiang Tao, Dachang Lu, Yongjie Yang, Yuan Ma, Yongxin Zhang, Sizhong Genet Mol Biol Cellular, Molecular and Developmental Genetics The mouse testis-enriched Znf230 gene, which encodes a type of RING finger protein, is present primarily in the nuclei of spermatogonia, the acrosome and the tail of spermatozoa. To investigate the role of Znf230 in spermatogenesis, we generated Znf230-deficient mice by disrupting Znf230 exon-5 and exon-6 using homologous recombination. The homozygous Znf230-knockout (KO) mice did not exhibit Znf230 mRNA expression and Znf230 protein production. Znf230 KO mice exhibited no obvious impairment in body growth or fertility. Male Znf230 KO mice had integral reproductive systems and mature sperm that were regular in number and shape. The developmental stages of male germ cells of Znf230 KO mice were also normal. We further examined variations in the transcriptomes of testicular tissue between Znf230 KO and wild-type mice through microarray analysis. The results showed that the mRNA level of one unclassified transcript 4921513I08Rik was increased and that the mRNA levels of three other transcripts, i.e., 4930448A20Rik, 4931431B13Rik and potassium channel tetramerisation domain containing 14(Kctd14), were reduced more than two-fold in Znf230 KO mice compared with wild-type mice. Using our current examination techniques, these findings suggested that Znf230 deficiency in mice may not affect growth, fertility or spermatogenesis. Sociedade Brasileira de Genética 2014-10 2014-10-21 /pmc/articles/PMC4261971/ /pubmed/25505846 http://dx.doi.org/10.1590/S1415-47572014005000013 Text en Copyright © 2014, Sociedade Brasileira de Genética. License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cellular, Molecular and Developmental Genetics Liu, Yunqiang Tao, Dachang Lu, Yongjie Yang, Yuan Ma, Yongxin Zhang, Sizhong Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility |
title | Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility |
title_full | Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility |
title_fullStr | Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility |
title_full_unstemmed | Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility |
title_short | Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility |
title_sort | targeted disruption of the mouse testis-enriched gene znf230 does not affect spermatogenesis or fertility |
topic | Cellular, Molecular and Developmental Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261971/ https://www.ncbi.nlm.nih.gov/pubmed/25505846 http://dx.doi.org/10.1590/S1415-47572014005000013 |
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