Key Laboratory for Animal Genetics & Molecular Breeding of Jiangsu Province, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
State-operated Haimen Breeding Goat Farm, Jiangsu 226000, China.
Genomics. 2021 Mar;113(2):463-473. doi: 10.1016/j.ygeno.2020.12.029. Epub 2021 Jan 20.
In Yangtze River Delta white goat, hypermethylation of CMTM3 leads to a decreased expression level in high quality brush hair. However, the regulation of CMTM3 expression and its function in hair follicle stem cells (HFSCs) remains largely unknown. In this study, we investigated the regulation of CMTM3 expression, function, and molecular mechanism in HFSCs. The re-expression of CMTM3 significantly suppressed the proliferation of HFSCs by inducing G1 cell cycle arrest and promoting apoptosis. Moreover, the downregulation of CMTM3 promoted HFSC proliferation. Treatment with sh_CMTM3 and incubation in a DHT culture medium had the most significant growth-promoting effect. It was hypothesized that transcriptome analysis using RNA sequencing (RNA-seq) in samples would enable the identification of unique protein-coding and non-coding genes that may help uncover the role of CMTM3. Multiple genes and pathways were involved in this process, including 168 common DEGs, such as CXCL8 and E-selectin, which is reportedly involved in multiple regulatory pathways. These results indicated that CMTM3 can function as HFSCs through the induction of a G1 cell cycle arrest and promoted apoptosis by mediating crosstalk between several pathways and transcription factors. Our data is available in the National Center for Biotechnology Information (NCBI) database with the accession number PRJNA657430.
在长江三角洲白山羊中,CMTM3 的高甲基化导致其在优质刷状毛中的表达水平降低。然而,CMTM3 在毛囊干细胞 (HFSCs) 中的表达调控及其功能仍知之甚少。在本研究中,我们研究了 CMTM3 在 HFSCs 中的表达调控、功能及其分子机制。CMTM3 的重新表达通过诱导 G1 细胞周期停滞和促进细胞凋亡,显著抑制 HFSCs 的增殖。此外,下调 CMTM3 促进了 HFSC 的增殖。sh_CMTM3 的处理和在 DHT 培养基中孵育具有最显著的促生长作用。据推测,使用 RNA 测序 (RNA-seq) 对样本进行转录组分析,可以鉴定出独特的编码和非编码蛋白基因,这可能有助于揭示 CMTM3 的作用。该过程涉及多个基因和途径,包括 168 个共同的差异表达基因,如 CXCL8 和 E-选择素,据报道这些基因参与多个调节途径。这些结果表明,CMTM3 可以通过介导几个途径和转录因子之间的串扰,诱导 G1 细胞周期停滞和促进细胞凋亡,从而在 HFSCs 中发挥作用。我们的数据可在国家生物技术信息中心 (NCBI) 数据库中获得,登录号为 PRJNA657430。