Yang S, Fan R, Shi Z, Ji K, Zhang J, Wang H, Herrid M, Zhang Q, Yao J, Smith G W, Dong C
J Anim Sci. 2015 Apr;93(4):1622-31. doi: 10.2527/jas.2014-8404.
The molecular mechanisms underlying the formation of coat colors in animals are poorly understood. Recent studies have demonstrated that microRNA play important roles in the control of melanogenesis and coat color in mammals. In a previous study, we characterized the miRNA expression profiles in alpaca skin with brown and white coat color and identified a novel miRNA (named lpa-miR-nov-66) that is expressed significantly higher in white skin compared to brown skin. The present study was conducted to determine the functional roles of this novel miRNA in the regulation of melanogenesis in alpaca melanocytes. lpa-miR-nov-66 is predicted to target the soluble guanylate cyclase (sGC) gene based on presence of a binding site in the sGC coding sequence (CDS). Overexpression of lpa-miR-nov-66 in alpaca melanocyes upregulated the expression of sGC both at the mRNA and protein level. Overexpression of lpa-miR-nov-66 in melanocyes also resulted in decreased expression of key melanogenic genes including tyrosinase (TYR), tyrosinase related protein 1 (TYRP1), and microphthalmia transcription factor (MITF). Our ELISA assays showed increased cyclic guanosine monophosphate (cGMP) but decreased cyclic adenosine monophosphate (cAMP) production in melanocytes overexpressing lpa-miR-nov-66. In addition, overexpression of lpa-miR-nov-66 also reduced melanin production in cultured melanocytes. Results support a role of lpa-miR-nov-66 in melanocytes by directly or indirectly targeting , which regulates melanogenesis via the cAMP pathway.
动物毛色形成背后的分子机制尚不清楚。最近的研究表明,微小RNA在哺乳动物黑色素生成和毛色控制中发挥重要作用。在之前的一项研究中,我们对棕色和白色毛色羊驼皮肤中的微小RNA表达谱进行了表征,并鉴定出一种新型微小RNA(命名为lpa-miR-nov-66),其在白色皮肤中的表达明显高于棕色皮肤。本研究旨在确定这种新型微小RNA在羊驼黑色素细胞黑色素生成调节中的功能作用。基于可溶性鸟苷酸环化酶(sGC)编码序列(CDS)中存在结合位点,预测lpa-miR-nov-66靶向sGC基因。在羊驼黑色素细胞中过表达lpa-miR-nov-66会在mRNA和蛋白质水平上上调sGC的表达。在黑色素细胞中过表达lpa-miR-nov-66还导致关键黑色素生成基因的表达降低,包括酪氨酸酶(TYR)、酪氨酸酶相关蛋白1(TYRP1)和小眼畸形相关转录因子(MITF)。我们的ELISA分析表明,过表达lpa-miR-nov-66的黑色素细胞中,环磷酸鸟苷(cGMP)增加,但环磷酸腺苷(cAMP)产生减少。此外,过表达lpa-miR-nov-66也降低了培养的黑色素细胞中黑色素的产生。结果支持lpa-miR-nov-66通过直接或间接靶向sGC在黑色素细胞中发挥作用,sGC通过cAMP途径调节黑色素生成。