Institute of Gene Science and Industrialization for Bamboo and Rattan Resources, International Center for Bamboo and Rattan, Beijing 100102, China.
Key Laboratory of National Forestry and Grassland Administration/Beijing for Bamboo & Rattan Science and Technology, Beijing 100102, China.
Int J Mol Sci. 2022 Oct 19;23(20):12568. doi: 10.3390/ijms232012568.
The Kelch repeat F-box (KFB) protein is an important E3 ubiquitin ligase that has been demonstrated to perform an important post-translational regulatory role in plants by mediating multiple biological processes. Despite their importance, KFBs have not yet been identified and characterized in bamboo. In this study, 19 PeKFBs were identified with F-box and Kelch domains; genes encoding these PeKFBs were unevenly distributed across 12 chromosomes of moso bamboo. Phylogenetic analysis indicated that the PeKFBs were divided into eight subclades based on similar gene structures and highly conserved motifs. A tissue-specific gene expression analysis showed that the s were differentially expressed in various tissues of moso bamboo. All the promoters of the s contained stress-related -elements, which was supported by the differentially expression of s of moso bamboo under drought and cold stresses. Sixteen proteins were screened from the moso bamboo shoots' cDNA library using PeKFB9 as a bait through a yeast two-hybrid (Y2H) assay. Moreover, PeKFB9 physically interacted with PeSKP1-like-1 and PePRX72-1, which mediated the activity of peroxidase in proteolytic turnover. Taken together, these findings improved our understanding of PeKFBs, especially in response to stresses, and laid a foundation for revealing the molecular mechanism of PeKFB9 in regulating lignin polymerization by degrading peroxidase.
Kelch 重复 F -box (KFB) 蛋白是一种重要的 E3 泛素连接酶,已被证明通过介导多种生物过程在植物中发挥重要的翻译后调控作用。尽管它们很重要,但竹子中的 KFB 尚未被鉴定和表征。在这项研究中,鉴定了 19 个 PeKFB,它们具有 F 框和 Kelch 结构域;这些 PeKFB 的基因编码不均匀分布在毛竹的 12 条染色体上。系统发育分析表明,PeKFB 根据相似的基因结构和高度保守的基序分为八个亚簇。组织特异性基因表达分析表明,在毛竹的不同组织中存在差异表达。所有 PeKFB 的启动子都含有与应激相关的元件,这得到了毛竹在干旱和寒冷胁迫下 PeKFB 差异表达的支持。通过酵母双杂交 (Y2H) 试验,从毛竹芽 cDNA 文库中筛选了 16 种蛋白质,使用 PeKFB9 作为诱饵。此外,PeKFB9 与 PeSKP1-like-1 和 PePRX72-1 物理相互作用,后者介导了过氧化物酶在蛋白水解循环中的活性。综上所述,这些发现提高了我们对 PeKFB 的理解,特别是在应对应激方面,并为揭示 PeKFB9 通过降解过氧化物酶调节木质素聚合的分子机制奠定了基础。