Profiling of miRNAs in porcine Sertoli cells.

MicroRNAs Pig Sertoli cell Spermatogenesis TRAF3

Journal

Journal of animal science and biotechnology
ISSN: 1674-9782
Titre abrégé: J Anim Sci Biotechnol
Pays: England
ID NLM: 101581293

Informations de publication

Date de publication:
2020
Historique:
received: 09 01 2020
accepted: 12 06 2020
entrez: 22 8 2020
pubmed: 22 8 2020
medline: 22 8 2020
Statut: epublish

Résumé

Sertoli cells (SCs) create a specialized environment to support and dictate spermatogenesis. MicroRNAs (miRNAs), a kind of ~ 22 nt small noncoding RNAs, have been reported to be highly abundant in mouse SCs and play critical roles in spermatogenesis. However, the miRNAs of porcine SCs remain largely unknown. We isolated porcine SCs and conducted small RNA sequencing. By comparing miRNAs in germ cells, we systematically analyzed the miRNA expression pattern of porcine SCs. We screened the highly enriched SC miRNAs and predicted their functions by Gene Ontology analysis. The dual luciferase assay was used to elucidate the regulation of tumor necrosis factor receptor (TNFR)-associated factor 3 ( The analysis showed that 18 miRNAs were highly expressed in SCs and 15 miRNAs were highly expressed in germ cells. These miRNAs were predicted to mediate SC and germ cell functions. In addition, Our findings provide novel insights into the miRNA expression pattern and their regulatory roles of porcine SCs.

Sections du résumé

BACKGROUND BACKGROUND
Sertoli cells (SCs) create a specialized environment to support and dictate spermatogenesis. MicroRNAs (miRNAs), a kind of ~ 22 nt small noncoding RNAs, have been reported to be highly abundant in mouse SCs and play critical roles in spermatogenesis. However, the miRNAs of porcine SCs remain largely unknown.
METHODS METHODS
We isolated porcine SCs and conducted small RNA sequencing. By comparing miRNAs in germ cells, we systematically analyzed the miRNA expression pattern of porcine SCs. We screened the highly enriched SC miRNAs and predicted their functions by Gene Ontology analysis. The dual luciferase assay was used to elucidate the regulation of tumor necrosis factor receptor (TNFR)-associated factor 3 (
RESULTS RESULTS
The analysis showed that 18 miRNAs were highly expressed in SCs and 15 miRNAs were highly expressed in germ cells. These miRNAs were predicted to mediate SC and germ cell functions. In addition,
CONCLUSION CONCLUSIONS
Our findings provide novel insights into the miRNA expression pattern and their regulatory roles of porcine SCs.

Identifiants

pubmed: 32821380
doi: 10.1186/s40104-020-00487-6
pii: 487
pmc: PMC7429792
doi:

Types de publication

Journal Article

Langues

eng

Pagination

85

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Xiaoxu Chen (X)

College of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, 723001 China.
Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Yi Zheng (Y)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Xueliang Li (X)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Qiang Gao (Q)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Tongying Feng (T)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Pengfei Zhang (P)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Mingzhi Liao (M)

College of Life Science, Northwest A&F University, Yangling, 712100 Shaanxi China.

Xiu'e Tian (X)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Hongzhao Lu (H)

College of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, 723001 China.

Wenxian Zeng (W)

Key Laboratory of Animal Genetics, Breeding and Reproduction of the Ministry of Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling, 712100 Shaanxi China.

Classifications MeSH