Min Ling, Hu Qin, Li Yaoyao, Xu Jiao, Ma Yizan, Zhu Longfu, Yang Xiyan, Zhang Xianlong
National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan, Hubei 430070, China.
National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan, Hubei 430070, China
Plant Physiol. 2015 Dec;169(4):2805-21. doi: 10.1104/pp.15.01480. Epub 2015 Oct 21.
Somatic embryogenesis (SE) is an efficient tool for the propagation of plant species and also, a useful model for studying the regulatory networks in embryo development. However, the regulatory networks underlying the transition from nonembryogenic callus to somatic embryos during SE remain poorly understood. Here, we describe an upland cotton (Gossypium hirsutum) CASEIN KINASE I gene, GhCKI, which is a unique key regulatory factor that strongly affects SE. Overexpressing GhCKI halted the formation of embryoids and plant regeneration because of a block in the transition from nonembryogenic callus to somatic embryos. In contrast, defective GhCKI in plants facilitated SE. To better understand the mechanism by which GhCKI regulates SE, the regulatory network was analyzed. A direct upstream negative regulator protein, cotton LEAFY COTYLEDON1, was identified to be targeted to a cis-element, CTTTTC, in the promoter of GhCKI. Moreover, GhCKI interacted with and phosphorylated cotton CINCINNATA-like TEOSINTE BRANCHED1-CYCLOIDEA-PCF transcription factor15 by coordinately regulating the expression of cotton PHYTOCHROME INTERACTING FACTOR4, finally disrupting auxin homeostasis, which led to increased cell proliferation and aborted somatic embryo formation in GhCKI-overexpressing somatic cells. Our results show a complex process of SE that is negatively regulated by GhCKI through a complex regulatory network.
体细胞胚胎发生(SE)是植物物种繁殖的有效工具,也是研究胚胎发育调控网络的有用模型。然而,在体细胞胚胎发生过程中,从非胚性愈伤组织向体细胞胚胎转变的调控网络仍知之甚少。在此,我们描述了一个陆地棉(Gossypium hirsutum)酪蛋白激酶I基因GhCKI,它是一个强烈影响体细胞胚胎发生的独特关键调控因子。过表达GhCKI会阻止胚状体的形成和植株再生,因为从非胚性愈伤组织向体细胞胚胎的转变受阻。相反,植物中功能缺陷的GhCKI促进了体细胞胚胎发生。为了更好地理解GhCKI调控体细胞胚胎发生的机制,我们分析了其调控网络。发现一种直接上游负调控蛋白棉花LEAFY COTYLEDON1靶向GhCKI启动子中的顺式元件CTTTTC。此外,GhCKI通过协同调节棉花PHYTOCHROME INTERACTING FACTOR4的表达,与棉花CINCINNATA样TEOSINTE BRANCHED1-CYCLOIDEA-PCF转录因子15相互作用并使其磷酸化,最终破坏生长素稳态,导致过表达GhCKI的体细胞中细胞增殖增加和体细胞胚胎形成失败。我们的结果表明,体细胞胚胎发生是一个复杂的过程,GhCKI通过一个复杂的调控网络对其进行负调控。