CircERCC6 Positively Regulates the Induced Activation of SHF Stem Cells in Cashmere Goats via the miR-412-3p/BNC2 Axis in an m6A-Dependent Manner
Author:
Zhang Qi1, Fan Yixing1, Bai Man1, Zhu Yubo1, Wang Zeying1, Shen Jincheng1, Xu Ruqing1, Zheng Wenxin23, Bai Wenlin1
Affiliation:
1. College of Animal Science & Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China 2. State Key Laboratory for Herbivorous Livestock Genetic Improvement and Germplasm Innovation of Ministry of Science and Technology and Xinjiang Uygur Autonomous Region, Urumqi 830011, China 3. Xinjiang Academy of Animal Sciences, Urumqi 830011, China
Abstract
The cashmere, a kind of nature protein fiber, is one of the main use of cashmere goats. The induced activation of secondary hair follicle (SHF) stem cells by the dermal papilla cell-derived signals is a key biological process for the morphogenesis and growth of cashmere fiber in cashmere goats. Previously, the circRNA-ERCC6 (circERCC6) was identified from cashmere goat SHFs; however, its biological significance is unclear in the SHF physiology process of cashmere goats. In this study, we found that circERCC6 exhibited significantly higher expression at anagen SHF bulge compared with the counterpart of telogen and harbored three m6A modified sites (named m6A-685, m6A-862, and m6A-995) through methylation immunoprecipitation using a real-time quantitative polymerase chain reaction (Me-RIP-qPCR) technique. The knockdown experiments of circERCC6 in SHF stem cells showed that circERCC6 positively regulates the induced activation of SHF stem cells in cashmere goats. Through a dual-luciferase reporter assay, we demonstrated that m6A-modified circERCC6 (m6A-circERCC6) sponged miR-412-3p to upregulate the expression of BNC2 mRNA in SHFstem cells. Through m6A-deficient mutant assay in circERCC6 knockdown SHF stem cells, we further showed that m6A modification within circERCC6 is required to mediate the miR-412-3p/BNC2 axis to finally promote the proper induced activation of SHF stem cells in cashmere goats.
Funder
National Natural Science Foundation of China Xinjiang Uygur Autonomous Region Scientific Research Innovation Platform Construction Project
Reference37 articles.
1. Wang, S., Ge, W., Luo, Z., Guo, Y., Jiao, B., Qu, L., Zhang, Z., and Wang, X. (2017). Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus). BMC Genom., 18. 2. CircRNA-1967 participates in the differentiation of goat SHF-SCs into hair follicle lineage by sponging miR-93-3p to enhance LEF1 expression;Zhu;Anim. Biotechnol.,2023 3. Ji, X.Y., Wang, J.X., Liu, B., Zheng, Z.Q., Fu, S.Y., Tarekegn, G.M., Bai, X., Bai, Y.S., Li, H., and Zhang, W.G. (2016). Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats. PLoS ONE, 11. 4. The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells;Aamar;Cell Rep.,2018 5. Exosomal Micro RNAs Derived from Dermal Papilla Cells Mediate Hair Follicle Stem Cell Proliferation and Differentiation;Yan;Int. J. Biol. Sci.,2019
|
|