Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters

Abstract Background Chickens play a crucial role as the primary global source of eggs and poultry, and the quality of rooster semen significantly impacts poultry reproductive efficiency. Therefore, it is imperative to comprehend the regulatory mechanisms underlying sperm development. Results In this...

Full description

Saved in:
Bibliographic Details
Main Authors: Shihao Guo, Bailin Cong, Liyang Zhu, Yao Zhang, Ying Yang, Xiaolong Qi, Xiangguo Wang, Longfei Xiao, Cheng Long, Yaxi Xu, Xihui Sheng
Format: Article
Language:English
Published: BMC 2024-11-01
Series:BMC Genomics
Subjects:
Online Access:https://doi.org/10.1186/s12864-024-10836-8
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846172226547613696
author Shihao Guo
Bailin Cong
Liyang Zhu
Yao Zhang
Ying Yang
Xiaolong Qi
Xiangguo Wang
Longfei Xiao
Cheng Long
Yaxi Xu
Xihui Sheng
author_facet Shihao Guo
Bailin Cong
Liyang Zhu
Yao Zhang
Ying Yang
Xiaolong Qi
Xiangguo Wang
Longfei Xiao
Cheng Long
Yaxi Xu
Xihui Sheng
author_sort Shihao Guo
collection DOAJ
description Abstract Background Chickens play a crucial role as the primary global source of eggs and poultry, and the quality of rooster semen significantly impacts poultry reproductive efficiency. Therefore, it is imperative to comprehend the regulatory mechanisms underlying sperm development. Results In this study, we established transcriptome profiles of lncRNAs, miRNAs, and mRNAs in 3 testis tissues and 3 epididymis tissues from “Jing Hong No.1” roosters at 24, 35, and 64 weeks of age. Using the data, we conducted whole transcriptome analysis and constructed a ceRNA network. We detected 10 differentially expressed mRNAs (DEmRNAs), 33 differentially expressed lncRNAs (DElncRNAs), and 10 differentially expressed miRNAs (DEmiRNAs) in the testis, as well as 149 DEmRNAs, 12 DElncRNAs, and 10 DEmiRNAs in the epididymis. These genes were found to be involved in cell differentiation and development, as well as various signaling pathways such as GnRH, MAPK, TGF-β, mTOR, VEGF, and calcium ion pathways. Subsequently, we constructed two competing endogenous RNA (ceRNA) networks comprising DEmRNAs, DElncRNAs, and DEmiRNAs. Furthermore, we identified four crucial lncRNA-mRNA-miRNA interactions that govern specific biological processes in the chicken reproductive system: MSTRG.2423.1-gga-miR-1563-PPP3CA and MSTRG.10064.2-gga-miR-32-5p-GPR12 regulating sperm motility in the testis; MSTRG.152556.1-gga-miR-9-3p-GREM1/THYN1 governing immunomodulation in the epididymis; and MSTRG.124708.1-gga-miR-375-NDUFB9/YBX1 controlling epididymal sperm maturation and motility. Conclusions Whole transcriptome sequencing of chicken testis and epididymis screened several key genes and ceRNA regulatory networks, which may be involved in the regulation of epididymal immunity, spermatogenesis and sperm viability through the pathways of MAPK, TGF-β, mTOR, and calcium ion. These findings contribute to our comprehensive understanding of the intricate molecular processes underlying rooster spermatogenesis, maturation and motility.
format Article
id doaj-art-27f7a0d9f9584771a9620032da92f8f0
institution Kabale University
issn 1471-2164
language English
publishDate 2024-11-01
publisher BMC
record_format Article
series BMC Genomics
spelling doaj-art-27f7a0d9f9584771a9620032da92f8f02024-11-10T12:09:06ZengBMCBMC Genomics1471-21642024-11-0125111510.1186/s12864-024-10836-8Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roostersShihao Guo0Bailin Cong1Liyang Zhu2Yao Zhang3Ying Yang4Xiaolong Qi5Xiangguo Wang6Longfei Xiao7Cheng Long8Yaxi Xu9Xihui Sheng10Animal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAnimal Science and Technology College, Beijing University of AgricultureAbstract Background Chickens play a crucial role as the primary global source of eggs and poultry, and the quality of rooster semen significantly impacts poultry reproductive efficiency. Therefore, it is imperative to comprehend the regulatory mechanisms underlying sperm development. Results In this study, we established transcriptome profiles of lncRNAs, miRNAs, and mRNAs in 3 testis tissues and 3 epididymis tissues from “Jing Hong No.1” roosters at 24, 35, and 64 weeks of age. Using the data, we conducted whole transcriptome analysis and constructed a ceRNA network. We detected 10 differentially expressed mRNAs (DEmRNAs), 33 differentially expressed lncRNAs (DElncRNAs), and 10 differentially expressed miRNAs (DEmiRNAs) in the testis, as well as 149 DEmRNAs, 12 DElncRNAs, and 10 DEmiRNAs in the epididymis. These genes were found to be involved in cell differentiation and development, as well as various signaling pathways such as GnRH, MAPK, TGF-β, mTOR, VEGF, and calcium ion pathways. Subsequently, we constructed two competing endogenous RNA (ceRNA) networks comprising DEmRNAs, DElncRNAs, and DEmiRNAs. Furthermore, we identified four crucial lncRNA-mRNA-miRNA interactions that govern specific biological processes in the chicken reproductive system: MSTRG.2423.1-gga-miR-1563-PPP3CA and MSTRG.10064.2-gga-miR-32-5p-GPR12 regulating sperm motility in the testis; MSTRG.152556.1-gga-miR-9-3p-GREM1/THYN1 governing immunomodulation in the epididymis; and MSTRG.124708.1-gga-miR-375-NDUFB9/YBX1 controlling epididymal sperm maturation and motility. Conclusions Whole transcriptome sequencing of chicken testis and epididymis screened several key genes and ceRNA regulatory networks, which may be involved in the regulation of epididymal immunity, spermatogenesis and sperm viability through the pathways of MAPK, TGF-β, mTOR, and calcium ion. These findings contribute to our comprehensive understanding of the intricate molecular processes underlying rooster spermatogenesis, maturation and motility.https://doi.org/10.1186/s12864-024-10836-8RoosterTestisEpididymisceRNAWhole transcriptome
spellingShingle Shihao Guo
Bailin Cong
Liyang Zhu
Yao Zhang
Ying Yang
Xiaolong Qi
Xiangguo Wang
Longfei Xiao
Cheng Long
Yaxi Xu
Xihui Sheng
Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
BMC Genomics
Rooster
Testis
Epididymis
ceRNA
Whole transcriptome
title Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
title_full Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
title_fullStr Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
title_full_unstemmed Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
title_short Whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
title_sort whole transcriptome sequencing of testis and epididymis reveals genes associated with sperm development in roosters
topic Rooster
Testis
Epididymis
ceRNA
Whole transcriptome
url https://doi.org/10.1186/s12864-024-10836-8
work_keys_str_mv AT shihaoguo wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT bailincong wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT liyangzhu wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT yaozhang wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT yingyang wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT xiaolongqi wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT xiangguowang wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT longfeixiao wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT chenglong wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT yaxixu wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters
AT xihuisheng wholetranscriptomesequencingoftestisandepididymisrevealsgenesassociatedwithspermdevelopmentinroosters