Cargando…

Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)

Sperm motility is an important standard to measure the fertility of male. In our previous study, we found that the diploid spermatozoa from allotetraploid hybrid (4nAT) had longer durations of rapid and slow progressive motility than haploid spermatozoa from common carp (COC). In this study, to expl...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Fangzhou, Xu, Kang, Zhou, Yunfan, Wu, Chang, Wang, Shi, Xiao, Jun, Wen, Min, Zhao, Rurong, Luo, Kaikun, Tao, Min, Duan, Wei, Liu, Shaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441299/
https://www.ncbi.nlm.nih.gov/pubmed/28340181
http://dx.doi.org/10.1093/biolre/iox010
_version_ 1783238237993566208
author Hu, Fangzhou
Xu, Kang
Zhou, Yunfan
Wu, Chang
Wang, Shi
Xiao, Jun
Wen, Min
Zhao, Rurong
Luo, Kaikun
Tao, Min
Duan, Wei
Liu, Shaojun
author_facet Hu, Fangzhou
Xu, Kang
Zhou, Yunfan
Wu, Chang
Wang, Shi
Xiao, Jun
Wen, Min
Zhao, Rurong
Luo, Kaikun
Tao, Min
Duan, Wei
Liu, Shaojun
author_sort Hu, Fangzhou
collection PubMed
description Sperm motility is an important standard to measure the fertility of male. In our previous study, we found that the diploid spermatozoa from allotetraploid hybrid (4nAT) had longer durations of rapid and slow progressive motility than haploid spermatozoa from common carp (COC). In this study, to explore sperm motility-related molecular mechanisms, we compared the testis tissues transcriptomes from 2-year-old male COC and 4nAT. The RNA-seq data revealed that 2985 genes were differentially expressed between COC and 4nAT, including 2216 upregulated and 769 downregulated genes in 4nAT. Some differentially expressed genes, such as tubulin genes, dynein, axonemal, heavy chain(dnah) genes, mitogen-activated protein kinase(mapk) genes, tektin 4, FOX transcription factors, proteasome genes, and ubiquitin carboxyl-terminal hydrolase(uchl) genes, are involved in the regulation of cell division, flagellar and ciliary motility, gene transcription, cytoskeleton, energy metabolism, and the ubiquitin–proteasome system, suggesting that these genes were related to sperm motility of the 4nAT. We confirmed the differential expression of 12 such genes in 4nAT by quantitative PCR. By western blotting, we also confirmed increased expression of Uchl3 in 4nAT testis. In addition, we identified 1915 and 2551 predicted long noncoding RNA (lncRNA) transcripts from testis tissue transcriptomes of COC and 4nAT, respectively. Of these, 1575 lncRNAs were specifically expressed in 4nAT and 939 were specifically expressed in COC. This study provides insights into the transcriptome profile of testis tissues from diploid and tetraploid, which are useful for research on regulatory mechanisms behind sperm motility in male polyploidy.
format Online
Article
Text
id pubmed-5441299
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-54412992018-02-23 Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†) Hu, Fangzhou Xu, Kang Zhou, Yunfan Wu, Chang Wang, Shi Xiao, Jun Wen, Min Zhao, Rurong Luo, Kaikun Tao, Min Duan, Wei Liu, Shaojun Biol Reprod Testis Sperm motility is an important standard to measure the fertility of male. In our previous study, we found that the diploid spermatozoa from allotetraploid hybrid (4nAT) had longer durations of rapid and slow progressive motility than haploid spermatozoa from common carp (COC). In this study, to explore sperm motility-related molecular mechanisms, we compared the testis tissues transcriptomes from 2-year-old male COC and 4nAT. The RNA-seq data revealed that 2985 genes were differentially expressed between COC and 4nAT, including 2216 upregulated and 769 downregulated genes in 4nAT. Some differentially expressed genes, such as tubulin genes, dynein, axonemal, heavy chain(dnah) genes, mitogen-activated protein kinase(mapk) genes, tektin 4, FOX transcription factors, proteasome genes, and ubiquitin carboxyl-terminal hydrolase(uchl) genes, are involved in the regulation of cell division, flagellar and ciliary motility, gene transcription, cytoskeleton, energy metabolism, and the ubiquitin–proteasome system, suggesting that these genes were related to sperm motility of the 4nAT. We confirmed the differential expression of 12 such genes in 4nAT by quantitative PCR. By western blotting, we also confirmed increased expression of Uchl3 in 4nAT testis. In addition, we identified 1915 and 2551 predicted long noncoding RNA (lncRNA) transcripts from testis tissue transcriptomes of COC and 4nAT, respectively. Of these, 1575 lncRNAs were specifically expressed in 4nAT and 939 were specifically expressed in COC. This study provides insights into the transcriptome profile of testis tissues from diploid and tetraploid, which are useful for research on regulatory mechanisms behind sperm motility in male polyploidy. Oxford University Press 2017-04 2017-03-07 /pmc/articles/PMC5441299/ /pubmed/28340181 http://dx.doi.org/10.1093/biolre/iox010 Text en © The Authors 2017. Published by Oxford University Press on behalf of Society for the Study of Reproduction. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Testis
Hu, Fangzhou
Xu, Kang
Zhou, Yunfan
Wu, Chang
Wang, Shi
Xiao, Jun
Wen, Min
Zhao, Rurong
Luo, Kaikun
Tao, Min
Duan, Wei
Liu, Shaojun
Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
title Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
title_full Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
title_fullStr Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
title_full_unstemmed Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
title_short Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
title_sort different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish(†)
topic Testis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441299/
https://www.ncbi.nlm.nih.gov/pubmed/28340181
http://dx.doi.org/10.1093/biolre/iox010
work_keys_str_mv AT hufangzhou differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT xukang differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT zhouyunfan differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT wuchang differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT wangshi differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT xiaojun differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT wenmin differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT zhaorurong differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT luokaikun differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT taomin differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT duanwei differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish
AT liushaojun differentexpressionpatternsofspermmotilityrelatedgenesintestisofdiploidandtetraploidcyprinidfish