DNA Methylation may be a testicular plateau adaptation in Tibetan pig
DNA methylation plays an important role in reproduction. Tibetan pigs maintain high sperm motility, even under extreme conditions at high altitudes. However, the DNA methylation mechanisms underlying testicular plateau adaptations in Tibetan pigs remain unclear. We determined the genomic DNA methyla...
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doaj-a2acb41954d6433b89417f3ed6eb80862021-02-18T10:31:38ZengTaylor & Francis GroupJournal of Applied Animal Research0971-21190974-18442021-01-01491626710.1080/09712119.2021.18824651882465DNA Methylation may be a testicular plateau adaptation in Tibetan pigYanling Zhao0Mengfang Tian1Zhipeng Cheng2Jianzhou Wang3Zili Ren4Tibet Agricultural and Animal Husbandry UniversityTibet Agricultural and Animal Husbandry UniversityTibet Agricultural and Animal Husbandry UniversityTibet Agricultural and Animal Husbandry UniversityTibet Agricultural and Animal Husbandry UniversityDNA methylation plays an important role in reproduction. Tibetan pigs maintain high sperm motility, even under extreme conditions at high altitudes. However, the DNA methylation mechanisms underlying testicular plateau adaptations in Tibetan pigs remain unclear. We determined the genomic DNA methylation level in the testicular tissues of Tibetan pigs living at high altitudes (TP) and of Yorkshire pigs that migrated to high altitudes (YP) using the fluorescence method. Quantitative real-time PCR and western blots were used to measure the gene and protein expression levels, respectively, of three DNA methyltransferases (DNMT1, DNMT3A, and DNMT3B) and hypoxia-inducible factor 2α (HIF2α). We found that the genomic DNA methylation level and the mRNA and protein expression levels of the four genes were all significantly lower in the testicular tissues of TP than YP. In short, compared with YP, the downregulation of DNA methyltransferases in the TP testes led to lower levels of genomic DNA methylation, which would facilitate higher sperm motility. Meanwhile, HIF2α expression in the TP testes was down-regulated, which might contributes to TP testes’ adaption to the plateau environment. This study provided new insights into the DNA methylation mechanisms underlying plateau adaptations in TP testicles.http://dx.doi.org/10.1080/09712119.2021.1882465dna methylationtibetan pig testiclesplateau adaptation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yanling Zhao Mengfang Tian Zhipeng Cheng Jianzhou Wang Zili Ren |
spellingShingle |
Yanling Zhao Mengfang Tian Zhipeng Cheng Jianzhou Wang Zili Ren DNA Methylation may be a testicular plateau adaptation in Tibetan pig Journal of Applied Animal Research dna methylation tibetan pig testicles plateau adaptation |
author_facet |
Yanling Zhao Mengfang Tian Zhipeng Cheng Jianzhou Wang Zili Ren |
author_sort |
Yanling Zhao |
title |
DNA Methylation may be a testicular plateau adaptation in Tibetan pig |
title_short |
DNA Methylation may be a testicular plateau adaptation in Tibetan pig |
title_full |
DNA Methylation may be a testicular plateau adaptation in Tibetan pig |
title_fullStr |
DNA Methylation may be a testicular plateau adaptation in Tibetan pig |
title_full_unstemmed |
DNA Methylation may be a testicular plateau adaptation in Tibetan pig |
title_sort |
dna methylation may be a testicular plateau adaptation in tibetan pig |
publisher |
Taylor & Francis Group |
series |
Journal of Applied Animal Research |
issn |
0971-2119 0974-1844 |
publishDate |
2021-01-01 |
description |
DNA methylation plays an important role in reproduction. Tibetan pigs maintain high sperm motility, even under extreme conditions at high altitudes. However, the DNA methylation mechanisms underlying testicular plateau adaptations in Tibetan pigs remain unclear. We determined the genomic DNA methylation level in the testicular tissues of Tibetan pigs living at high altitudes (TP) and of Yorkshire pigs that migrated to high altitudes (YP) using the fluorescence method. Quantitative real-time PCR and western blots were used to measure the gene and protein expression levels, respectively, of three DNA methyltransferases (DNMT1, DNMT3A, and DNMT3B) and hypoxia-inducible factor 2α (HIF2α). We found that the genomic DNA methylation level and the mRNA and protein expression levels of the four genes were all significantly lower in the testicular tissues of TP than YP. In short, compared with YP, the downregulation of DNA methyltransferases in the TP testes led to lower levels of genomic DNA methylation, which would facilitate higher sperm motility. Meanwhile, HIF2α expression in the TP testes was down-regulated, which might contributes to TP testes’ adaption to the plateau environment. This study provided new insights into the DNA methylation mechanisms underlying plateau adaptations in TP testicles. |
topic |
dna methylation tibetan pig testicles plateau adaptation |
url |
http://dx.doi.org/10.1080/09712119.2021.1882465 |
work_keys_str_mv |
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1724263583670337536 |