Yin Ronghuan, Yin Ronglan, Bai Man, Fan Yixing, Wang Zeying, Zhu Yubo, Zhang Qi, Hui Taiyu, Shen Jincheng, Feng Siyu, Bai Wenlin
College of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.
Research Academy of Animal Husbandry and Veterinary Medicine Sciences of Jilin Province, Changchun, 130062, China.
Anim Biosci. 2023 Apr;36(4):555-569. doi: 10.5713/ab.22.0211. Epub 2022 Nov 14.
The objective of this study was to investigate the effects of N6-Methyladenosine modification-circRNA-zinc finger protein 638 (m6A-circRNA-ZNF638) on the induced activation of secondary hair follicle (SHF) stem cells with its potential mechanisms in cashmere goats.
The m6A modification of ZNF638 was analyzed using methylation immunoprecipitation with real-time quantitative polymerase chain reaction technique in SHF stem cells. The effects of circRNA-ZNF638 on the induced activation of SHF stem cells in m6A dependence were evaluated through the overexpression of circRNA-ZNF638/its m6Adeficient mutants in circRNA-ZNF638 knockdown SHF stem cells. The competitive binding of miR-361-5p to circRNA-ZNF638/Wnt5a 3'- untranslated region was analyzed through Dual-luciferase reporter assay.
The m6A-circRNA-ZNF638 had significantly higher transcription at anagen SHF bulge of cashmere goats compared with that at telogen, as well as it positively regulated the induced activation of SHF-stem cells in cashmere goats. Mechanismly, m6A-circRNA-ZNF638 sponged miR-361-5p to heighten the transcriptional expression of Wnt5a gene in SHFstem cells. We further demonstrated that the internal m6A modification within circRNAZNF638 is required for mediating the miR-361-5p/Wnt5a pathway to regulate the induced activation of SHF stem cells through an introducing of m6A-deficient mutant of circRNAZNF638.
The circRNA-ZNF638 contributes the proper induced activation of SHF-stem cells in cashmere goats in m6A-dependent manner through miR-361-5p/Wnt5a axis.
本研究旨在探讨N6-甲基腺苷修饰的环状RNA-锌指蛋白638(m6A-circRNA-ZNF638)对绒山羊次级毛囊(SHF)干细胞诱导激活的影响及其潜在机制。
采用甲基化免疫沉淀结合实时定量聚合酶链反应技术分析SHF干细胞中ZNF638的m6A修饰。通过在敲低circRNA-ZNF638的SHF干细胞中过表达circRNA-ZNF638/其m6A缺陷突变体,评估circRNA-ZNF638对m6A依赖性SHF干细胞诱导激活的影响。通过双荧光素酶报告基因检测分析miR-361-5p与circRNA-ZNF638/Wnt5a 3'-非翻译区的竞争性结合。
与休止期相比,m6A-circRNA-ZNF638在绒山羊生长期SHF隆突处的转录水平显著更高,并且它正向调节绒山羊SHF干细胞的诱导激活。机制上,m6A-circRNA-ZNF638吸附miR-361-5p以提高SHF干细胞中Wnt5a基因的转录表达。我们进一步证明,通过引入circRNA-ZNF638的m6A缺陷突变体,circRNA-ZNF638内部的m6A修饰是介导miR-361-5p/Wnt5a通路调节SHF干细胞诱导激活所必需的。
circRNA-ZNF638通过miR-361-5p/Wnt5a轴以m6A依赖的方式促进绒山羊SHF干细胞的适当诱导激活。