He Songzhen, Tong Xiaoling, Lu Kunpeng, Lu Yaru, Luo Jiangwen, Yang Wenhao, Chen Min, Han Min-Jin, Hu Hai, Lu Cheng, Dai Fangyin
State Key Laboratory of Silkworm Genome Biology, Key Laboratory for Sericulture Functional Genomics and Biotechnology of Agricultural Ministry, Southwest University, Chongqing, 400715, China.
PLoS One. 2016 May 6;11(5):e0155061. doi: 10.1371/journal.pone.0155061. eCollection 2016.
As a source of insect polymorphism, melanism plays an important role in ecological adaption and usually endows advantageous phenotypic-effects on insects. However, due to the mechanistic diversity, there are knowledge gaps in the molecular mechanisms underlying melanism and the related phenotypes. In silk moths, a recessive melanic mutant (sex-controlled melanism, sml) strain exhibits extended adult longevity. We took a transcriptome approach to perform a comparative analysis between this sml strain and a wild-type strain (Dazao). Our analysis resulted in the identification of 59 unique differentially expressed genes in the melanic mutant. Two key genes (laccase2 and yellow) involved in melanin formation were significantly up-regulated in melanic individuals. The laccase2 B-type isoform (BGIBMGA006746) was found to likely participate in the silkworm cuticular melanism process at late pupal stage. Moreover, we discovered 22 cuticular protein encoding genes with the possible function in melanin transport and/or maintenance. Based on our findings, we presume that the longer survival of the melanic sml male moths might be associated with the enhanced antioxidant defense systems and a reduction in the insulin/IGF-1 signaling pathway (IIS). These findings will facilitate the understanding of the molecular basis underlying melanism and the derived phenotypic-effects.
作为昆虫多态性的一个来源,黑化现象在生态适应中起着重要作用,通常赋予昆虫有利的表型效应。然而,由于机制的多样性,黑化现象及相关表型背后的分子机制存在知识空白。在家蚕中,一个隐性黑化突变体(性控黑化,sml)品系表现出成虫寿命延长。我们采用转录组方法对该sml品系和野生型品系(大造)进行了比较分析。我们的分析结果鉴定出黑化突变体中有59个独特的差异表达基因。参与黑色素形成的两个关键基因(漆酶2和黄色)在黑化个体中显著上调。发现漆酶2 B型异构体(BGIBMGA006746)可能在蛹后期参与家蚕表皮黑化过程。此外,我们发现了22个可能在黑色素运输和/或维持中起作用的表皮蛋白编码基因。基于我们的发现,我们推测黑化的sml雄蛾寿命更长可能与抗氧化防御系统增强和胰岛素/胰岛素样生长因子-1信号通路(IIS)减少有关。这些发现将有助于理解黑化现象及衍生表型效应背后的分子基础。