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张力岚,杨军,王让剑. 茶树PALC4H4CL基因家族的全基因组鉴定及表达分析[J]. 茶叶学报,2024,65(3):34−46. DOI: 10.20045/j.cnki.issn.2096-0220.2024.03.003
引用本文: 张力岚,杨军,王让剑. 茶树PALC4H4CL基因家族的全基因组鉴定及表达分析[J]. 茶叶学报,2024,65(3):34−46. DOI: 10.20045/j.cnki.issn.2096-0220.2024.03.003
ZHANG Li-lan, YANG Jun, WANG Rang-jian. Identification and Expressions of PAL, C4H, and 4CL Families in Tea Plant[J]. ACTA TEA SINICA, 2024, 65(3): 34-46. DOI: 10.20045/j.cnki.issn.2096-0220.2024.03.003
Citation: ZHANG Li-lan, YANG Jun, WANG Rang-jian. Identification and Expressions of PAL, C4H, and 4CL Families in Tea Plant[J]. ACTA TEA SINICA, 2024, 65(3): 34-46. DOI: 10.20045/j.cnki.issn.2096-0220.2024.03.003

茶树PALC4H4CL基因家族的全基因组鉴定及表达分析

Identification and Expressions of PAL, C4H, and 4CL Families in Tea Plant

  • 摘要:
    目的 分析茶树PALC4H4CL基因家族成员的基本特征,探索它们与苯乙醇樱草糖苷含量性状之间的因果关系,对于深入研究PALC4H4CL基因家族在茶树上的生物学功能具有重要意义。
    方法 基于生物信息学方法及转录组测序技术,分析PALC4H4CL基因成员在茶树基因组中的分布、理化性质、基因结构、系统发育关系、启动子顺式作用元件与表达特性,以及探索茶树PALC4H4CL基因成员在苯乙醇樱草糖苷含量差异显著的茶树新品系(高糖苷和低糖苷品系)新梢中的表达差异。
    结果 7个CsPAL、4个CsC4H与4个Cs4CL基因分布在9条染色体上。所有CsPAL均只有1个内含子;除CsC4H4外,其他CsC4H成员均含有2个内含子;Cs4CL成员均含有多个内含子。系统进化分析表明,它们与杨树PAL、C4H和4CL蛋白的亲缘关系较近。基因结构和保守基序分析显示,亲缘关系较近的基因,其基因结构和保守基序的组成也较为相似。启动子顺式作用元件预测发现,CsPAL、CsC4HCs4CL基因成员的启动子区域内含有多种顺式元件,包括逆境胁迫响应、生长发育相关以及激素响应等多种顺式元件。转录组分析发现,大多数CsPALCsC4HCs4CL的成员表现为组织特异性表达,且会受到激素、低温、干旱及高盐的诱导。CsPAL7CsC4H4Cs4CL3在苯乙醇樱草糖苷含量明显差异的品系中存在表达差异,CsPAL7在高糖苷品系中的表达量要大于低糖苷品系,CsC4H4Cs4CL3在低糖苷品系中的表达量均显著高于高糖苷品系,推测这3个家族基因的表达可能对茶树新梢中苯乙醇樱草糖苷的形成起不同的作用。
    结论 本研究为PALC4H4CL基因的功能分析提供了有用的信息,其家族成员可作为茶树分子育种的候选基因。

     

    Abstract:
    Objective Genetic characteristics of PAL, C4H, and 4CL family members in tea were studied to examine the connection between these genes and abundance of phenylethanol primrose glycoside (PPG) in the plant.
    Method Using bioinformatics and transcriptome sequencing techniques, the distribution, physicochemical properties, gene structure, phylogenetic relationships, promoter cis-acting elements, and expression characteristics of CsPAL, CsC4H, and Cs4CLs in the genome of tea plants were analyzed. Expressions of these genes in the shoots of low- and high-glycoside teas, which differed significantly in PPG content, were compared.
    Result Seven CsPALs, 4 CsC4Hs, and 4 Cs4CLs were found in 9 chromosomes of tea plants. All CsPALs had only one intron, while all CsC4Hs other than CsC4H4 had two and all Cs4CLs had multiple introns. Phylogenetically, they closely related to PAL, C4H, and 4CL of Populus trichocarpa with a similarity in structure and conserved motifs. The promoter regions of CsPALs, CsC4Hs, and Cs4CLs contained elements responding to stresses, growth, development, and presence of hormones. The tissue specific gene expression could be induced by exposure to hormones, low temperature, drought, or high salinity. Significantly differentiated, CsPAL7 was highly expressed in the high-glycoside teas than the low-glycoside teas, but CsC4H4 and Cs4CL3 were the opposite. The varied expression patterns might indicate different roles these families played in the PPG formation in tea plants.
    Conclusion The information obtained on CsPALs, CsC4Hs, and Cs4CLs would be of value for the understanding of the biological functions of these genes and breeding new tea varieties.

     

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