Zhao Wei, Liu Yonghui, Li Lin, Meng Haijun, Yang Ying, Dong Zhaobin, Wang Lei, Wu Guoliang
College of Horticulture, Henan Agricultural University, Zhengzhou, China.
Henan Key Laboratory of Fruit and Cucurbit Biology, Zhengzhou, China.
Front Genet. 2021 Feb 24;12:632509. doi: 10.3389/fgene.2021.632509. eCollection 2021.
Basic helix-loop-helix (bHLH) proteins are transcription factors (TFs) that have been shown to regulate anthocyanin biosynthesis in many plant species. However, the gene family in walnut ( L.) has not yet been reported. In this study, 102 genes were identified in the walnut genome and were classified into 15 subfamilies according to sequence similarity and phylogenetic relationships. The gene structure, conserved domains, and chromosome location of the genes were analyzed by bioinformatic methods. Gene duplication analyses revealed that 42 were involved in the expansion of the walnut gene family. We also characterized -regulatory elements of these genes and performed Gene Ontology enrichment analysis of gene functions, and examined protein-protein interactions. Four candidate genes (, , , and ) were found to have high homology to genes encoding bHLH TFs involved in anthocyanin biosynthesis in other plants. RNA sequencing revealed tissue- and developmental stage-specific expression profiles and distinct expression patterns of according to phenotype (red vs. green leaves) and developmental stage in red walnut hybrid progeny, which were confirmed by quantitative real-time PCR analysis. All four of the candidate JrbHLH proteins localized to the nucleus, consistent with a TF function. These results provide a basis for the functional characterization of genes and investigations on the molecular mechanisms of anthocyanin biosynthesis in red walnut.
基本螺旋-环-螺旋(bHLH)蛋白是一类转录因子(TFs),已被证明在许多植物物种中调控花青素生物合成。然而,核桃(Juglans regia L.)中的该基因家族尚未见报道。本研究在核桃基因组中鉴定出102个bHLH基因,并根据序列相似性和系统发育关系将其分为15个亚家族。通过生物信息学方法分析了这些基因的基因结构、保守结构域和染色体定位。基因复制分析表明,42个bHLH基因参与了核桃bHLH基因家族的扩增。我们还对这些基因的顺式调控元件进行了表征,并对基因功能进行了基因本体富集分析,以及检测了蛋白质-蛋白质相互作用。发现四个候选基因(JrbHLH3、JrbHLH13、JrbHLH14和JrbHLH15)与其他植物中参与花青素生物合成的bHLH转录因子编码基因具有高度同源性。RNA测序揭示了红核桃杂交后代中根据表型(红叶与绿叶)和发育阶段的组织和发育阶段特异性表达谱以及JrbHLH基因的不同表达模式,这通过定量实时PCR分析得到了证实。所有四个候选JrbHLH蛋白都定位于细胞核,这与转录因子功能一致。这些结果为bHLH基因的功能表征以及红核桃花青素生物合成分子机制的研究提供了基础。