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LncRNA Gm2044 highly expresses in spermatocyte and inhibits Utf1 translation by interacting with Utf1 mRNA.
- Source :
-
Genes & genomics [Genes Genomics] 2018 Jul; Vol. 40 (7), pp. 781-787. Date of Electronic Publication: 2018 Apr 10. - Publication Year :
- 2018
-
Abstract
- Spermatogenesis is a process which includes the following phases: spermatogonial stem cell proliferation and differentiation, spermatogonia, spermatocyte, spermatid and mature sperm. Spermatogenic failure is the important factor resulting in male infertility. Recent studies showed that long noncoding RNA (lncRNA) have been found to be involved in the regulation of male reproduction. However, lncRNA associated with spermatogenesis and their mechanisms of action are unclear. The aim of this study is to explore the role and molecular mechanism of lncRNA in spermatogenesis. LncRNA microarray of germ cells and bioinformatic analysis showed lncRNA Gm2044 may play potential roles in spermatogenesis. The expression level of RNA and protein were analyzed by RT-qPCR and western blotting, respectively. The interaction of lncRNA with mRNA was detected by RNA pull down and cellular proliferation was measured using CCK-8 reagent. Testis-enriched lncRNA Gm2044 is abundant in mouse spermatocytes. Gm2044 can suppress the translation of adjacent spermatogenesis-related gene Utf1 by interacting with Utf1 mRNA. Furthermore, the proliferation of mouse spermatogonia GC-1 cell line and spermatocyte GC-2 cell line was inhibited by Gm2044.<br />Conclusion: LncRNA Gm2044 was identified to inhibit Utf1 mRNA translation and play important roles in spermatogenesis.
- Subjects :
- Animals
Cell Differentiation genetics
Cell Proliferation genetics
Gene Expression Regulation, Developmental
Male
Mice
RNA, Messenger genetics
Spermatocytes metabolism
Testis growth & development
Chromosomal Proteins, Non-Histone genetics
RNA, Long Noncoding genetics
Spermatocytes growth & development
Spermatogenesis genetics
Trans-Activators genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2092-9293
- Volume :
- 40
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Genes & genomics
- Publication Type :
- Academic Journal
- Accession number :
- 29934815
- Full Text :
- https://doi.org/10.1007/s13258-018-0690-4