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Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia

OBJECTIVE: Spermatogenesis is a complex process controlled by a plethora of genes. Changes in expression and function of these genes may thus lead to spermatogenic deficiency and male infertility. TEX11, TEX12, TEX14 and TEX15 are germ cell-specific genes expressed in the testis. TEX11, involved in...

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Autores principales: Boroujeni, Parnaz Borjian, Sabbaghian, Marjan, Totonchi, Mehdi, Sodeifi, Niloofar, Sarkardeh, Homa, Samadian, Azam, Sadighi-Gilani, Mohammad Ali, Gourabi, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106636/
https://www.ncbi.nlm.nih.gov/pubmed/29932616
http://dx.doi.org/10.5935/1518-0557.20180030
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author Boroujeni, Parnaz Borjian
Sabbaghian, Marjan
Totonchi, Mehdi
Sodeifi, Niloofar
Sarkardeh, Homa
Samadian, Azam
Sadighi-Gilani, Mohammad Ali
Gourabi, Hamid
author_facet Boroujeni, Parnaz Borjian
Sabbaghian, Marjan
Totonchi, Mehdi
Sodeifi, Niloofar
Sarkardeh, Homa
Samadian, Azam
Sadighi-Gilani, Mohammad Ali
Gourabi, Hamid
author_sort Boroujeni, Parnaz Borjian
collection PubMed
description OBJECTIVE: Spermatogenesis is a complex process controlled by a plethora of genes. Changes in expression and function of these genes may thus lead to spermatogenic deficiency and male infertility. TEX11, TEX12, TEX14 and TEX15 are germ cell-specific genes expressed in the testis. TEX11, involved in the initiation and maintenance of chromosome synapses in meiotic chromosomes, has been shown to be essential for meiosis and fertility in males. TEX14, a component of intercellular bridges in germ cells, is required for spermatogenesis and fertility. TEX12 and TEX15 are essential for correct assembly of the synaptonemal complex and thus meiosis progression. METHODS: In order to examine whether changes in expression of these genes is associated with impaired spermatogenesis, expression levels of these genes were quantified by RT-qPCR on samples retrieved from infertile patients submitted to diagnostic testicular biopsy at Royan institute. Samples were divided into two groups of 18 patients with non-obstructive azoospermia considered as case; nine patients with obstructive azoospermia were included in the control group. RESULTS: A significant down-regulation of these genes was observed in the SCOS group when compared to the control group. CONCLUSION: This result suggests that regular expression of TEX11, TEX12, TEX14 and TEX15 is essential for the early stages of spermatogenesis.
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spelling pubmed-61066362018-08-24 Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia Boroujeni, Parnaz Borjian Sabbaghian, Marjan Totonchi, Mehdi Sodeifi, Niloofar Sarkardeh, Homa Samadian, Azam Sadighi-Gilani, Mohammad Ali Gourabi, Hamid JBRA Assist Reprod Original Article OBJECTIVE: Spermatogenesis is a complex process controlled by a plethora of genes. Changes in expression and function of these genes may thus lead to spermatogenic deficiency and male infertility. TEX11, TEX12, TEX14 and TEX15 are germ cell-specific genes expressed in the testis. TEX11, involved in the initiation and maintenance of chromosome synapses in meiotic chromosomes, has been shown to be essential for meiosis and fertility in males. TEX14, a component of intercellular bridges in germ cells, is required for spermatogenesis and fertility. TEX12 and TEX15 are essential for correct assembly of the synaptonemal complex and thus meiosis progression. METHODS: In order to examine whether changes in expression of these genes is associated with impaired spermatogenesis, expression levels of these genes were quantified by RT-qPCR on samples retrieved from infertile patients submitted to diagnostic testicular biopsy at Royan institute. Samples were divided into two groups of 18 patients with non-obstructive azoospermia considered as case; nine patients with obstructive azoospermia were included in the control group. RESULTS: A significant down-regulation of these genes was observed in the SCOS group when compared to the control group. CONCLUSION: This result suggests that regular expression of TEX11, TEX12, TEX14 and TEX15 is essential for the early stages of spermatogenesis. Brazilian Society of Assisted Reproduction 2018 /pmc/articles/PMC6106636/ /pubmed/29932616 http://dx.doi.org/10.5935/1518-0557.20180030 Text en http://creativecommons.org/licenses/by/4.0/ 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 Original Article
Boroujeni, Parnaz Borjian
Sabbaghian, Marjan
Totonchi, Mehdi
Sodeifi, Niloofar
Sarkardeh, Homa
Samadian, Azam
Sadighi-Gilani, Mohammad Ali
Gourabi, Hamid
Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia
title Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia
title_full Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia
title_fullStr Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia
title_full_unstemmed Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia
title_short Expression analysis of genes encoding TEX11, TEX12, TEX14 and TEX15 in testis tissues of men with non-obstructive azoospermia
title_sort expression analysis of genes encoding tex11, tex12, tex14 and tex15 in testis tissues of men with non-obstructive azoospermia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106636/
https://www.ncbi.nlm.nih.gov/pubmed/29932616
http://dx.doi.org/10.5935/1518-0557.20180030
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