Zhang Qi, Fan Yixing, Bai Man, Zhu Yubo, Wang Zeying, Shen Jincheng, Xu Ruqing, Zheng Wenxin, Bai Wenlin
College of Animal Science & Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China.
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.
Animals (Basel). 2024 Jan 5;14(2):187. doi: 10.3390/ani14020187.
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 mA modified sites (named mA-685, mA-862, and mA-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 mA-modified circERCC6 (mA-circERCC6) sponged miR-412-3p to upregulate the expression of BNC2 mRNA in SHFstem cells. Through mA-deficient mutant assay in circERCC6 knockdown SHF stem cells, we further showed that mA 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.
羊绒是一种天然蛋白质纤维,是绒山羊的主要用途之一。真皮乳头细胞衍生信号诱导次级毛囊(SHF)干细胞的激活是绒山羊羊绒纤维形态发生和生长的关键生物学过程。此前,从绒山羊SHF中鉴定出了circRNA-ERCC6(circERCC6);然而,其在绒山羊SHF生理过程中的生物学意义尚不清楚。在本研究中,我们发现circERCC6在生长期SHF隆突处的表达明显高于休止期的对应部位,并且通过实时定量聚合酶链反应(Me-RIP-qPCR)技术进行甲基化免疫沉淀,发现其含有三个mA修饰位点(命名为mA-685、mA-862和mA-995)。在SHF干细胞中对circERCC6进行敲低实验表明,circERCC6正向调节绒山羊SHF干细胞的诱导激活。通过双荧光素酶报告基因测定,我们证明了mA修饰的circERCC6(mA-circERCC6)通过海绵吸附miR-412-3p来上调SHF干细胞中BNC2 mRNA的表达。通过在circERCC6敲低的SHF干细胞中进行mA缺陷突变体测定,我们进一步表明,circERCC6内的mA修饰是介导miR-412-3p/BNC2轴以最终促进绒山羊SHF干细胞正常诱导激活所必需的。