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Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes

The male infertility of cattleyak resulted from spermatogenic arrest has greatly restricted the effective utilization of the heterosis from crossbreeding of cattle and yak. Based on our previous studies, the significant divergences of the transcriptomic and proteomic sequencing between yak and cattl...

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Autores principales: Xu, Chuanfei, Shah, Mujahid ali, Mipam, TserangDonko, Wu, Shixin, Yi, Chuanping, Luo, Hui, Yuan, Meng, Chai, Zhixin, Zhao, Wangsheng, Cai, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949159/
https://www.ncbi.nlm.nih.gov/pubmed/31929752
http://dx.doi.org/10.7150/ijbs.38232
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author Xu, Chuanfei
Shah, Mujahid ali
Mipam, TserangDonko
Wu, Shixin
Yi, Chuanping
Luo, Hui
Yuan, Meng
Chai, Zhixin
Zhao, Wangsheng
Cai, Xin
author_facet Xu, Chuanfei
Shah, Mujahid ali
Mipam, TserangDonko
Wu, Shixin
Yi, Chuanping
Luo, Hui
Yuan, Meng
Chai, Zhixin
Zhao, Wangsheng
Cai, Xin
author_sort Xu, Chuanfei
collection PubMed
description The male infertility of cattleyak resulted from spermatogenic arrest has greatly restricted the effective utilization of the heterosis from crossbreeding of cattle and yak. Based on our previous studies, the significant divergences of the transcriptomic and proteomic sequencing between yak and cattleyak prompt us to investigate the critical roles of microRNAs in post-transcriptional regulation of gene expression during spermatogenesis. TUNEL-POD analysis presented sharply decreased spermatogenic cell types and the increased apoptotic spermatogonia in cattleyak. The STA-PUT velocity sedimentation was employed to obtain spermatogonia and spermatocytes from cattle, yak and cattleyak and these spermatogenic cells were verified by the morphological and phenotypic identification. MicroRNA microarray showed that 27 differentially expressed miRNAs were simultaneously identified both in cattleyak vs cattle and in cattleyak vs yak comparisons. Further analysis revealed that the down-regulation of bta-let-7 families, bta-miR-125 and bta-miR-23a might impair the RA-induced differentiation of spermatogonia. Target gene analysis for differentially expressed miRNAs revealed that miRNAs targeted major players involved in vesicle-mediated transport, regulation of protein kinase activity and Pathways in cancer. In addition, spermatogonia transfection analysis revealed that the down-regulation of bta-miR-449a in the cattleyak might block the transition of male germ cells from the mitotic cycle to the meiotic program. The present study provided valuable information for future elucidating the regulatory roles of miRNAs involved in spermatogenic arrest of cattleyak.
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spelling pubmed-69491592020-01-11 Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes Xu, Chuanfei Shah, Mujahid ali Mipam, TserangDonko Wu, Shixin Yi, Chuanping Luo, Hui Yuan, Meng Chai, Zhixin Zhao, Wangsheng Cai, Xin Int J Biol Sci Research Paper The male infertility of cattleyak resulted from spermatogenic arrest has greatly restricted the effective utilization of the heterosis from crossbreeding of cattle and yak. Based on our previous studies, the significant divergences of the transcriptomic and proteomic sequencing between yak and cattleyak prompt us to investigate the critical roles of microRNAs in post-transcriptional regulation of gene expression during spermatogenesis. TUNEL-POD analysis presented sharply decreased spermatogenic cell types and the increased apoptotic spermatogonia in cattleyak. The STA-PUT velocity sedimentation was employed to obtain spermatogonia and spermatocytes from cattle, yak and cattleyak and these spermatogenic cells were verified by the morphological and phenotypic identification. MicroRNA microarray showed that 27 differentially expressed miRNAs were simultaneously identified both in cattleyak vs cattle and in cattleyak vs yak comparisons. Further analysis revealed that the down-regulation of bta-let-7 families, bta-miR-125 and bta-miR-23a might impair the RA-induced differentiation of spermatogonia. Target gene analysis for differentially expressed miRNAs revealed that miRNAs targeted major players involved in vesicle-mediated transport, regulation of protein kinase activity and Pathways in cancer. In addition, spermatogonia transfection analysis revealed that the down-regulation of bta-miR-449a in the cattleyak might block the transition of male germ cells from the mitotic cycle to the meiotic program. The present study provided valuable information for future elucidating the regulatory roles of miRNAs involved in spermatogenic arrest of cattleyak. Ivyspring International Publisher 2020-01-01 /pmc/articles/PMC6949159/ /pubmed/31929752 http://dx.doi.org/10.7150/ijbs.38232 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Xu, Chuanfei
Shah, Mujahid ali
Mipam, TserangDonko
Wu, Shixin
Yi, Chuanping
Luo, Hui
Yuan, Meng
Chai, Zhixin
Zhao, Wangsheng
Cai, Xin
Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes
title Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes
title_full Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes
title_fullStr Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes
title_full_unstemmed Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes
title_short Bovid microRNAs involved in the process of spermatogonia differentiation into spermatocytes
title_sort bovid micrornas involved in the process of spermatogonia differentiation into spermatocytes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949159/
https://www.ncbi.nlm.nih.gov/pubmed/31929752
http://dx.doi.org/10.7150/ijbs.38232
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