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闽楠PIF基因家族鉴定和表达模式研究

Identification and Expression Analysis of the PIF Gene Family in Phoebe bournei

  • 摘要:
    目的 对闽楠光敏色素相互作用因子PIF家族进行鉴定,并探究其在生长发育中的功能。
    方法 利用生物信息学与荧光定量PCR等方法,对PbPIFs基因家族进行了全基因组鉴定,分析其蛋白理化特性、基因结构、进化关系、亚细胞定位及启动子顺式作用元件和光响应下的表达模式。
    结果 从闽楠全基因组中共鉴定出9个PbPIFs基因,具有高度保守的bHLH结构域,同时包含APA结构域或APB结构域。亚细胞定位结果显示PbPIFs蛋白均定位于细胞核。PbPIFs基因上游启动子区域存在光响应、干旱、低温及激素相关的顺式作用元件,其中ABA的响应元件数量最多。PbPIFs家族成员间表现出组织部位表达分化,同时荧光定量PCR结果表明PbPIF1PbPIF3aPbPIF3bPbPIF5等在光照诱导下表达显著下调,表明这些基因可能参与光形态建成。
    结论 闽楠9个PbPIFs基因间表现出功能分化,不同成员参与响应光信号及非生物胁迫等不同环境因子信号,研究结果为深入解析闽楠PIF家族成员的基因功能及其环境响应的调控机制提供科学依据。

     

    Abstract:
    Objective To identify the Phytochrome interacting factor (PIF) gene family in Phoebe bournei and explore their functions in growth and development.
    Method Bioinformatics and fluorescence quantitative PCR (qPCR) were used for genome-wide identification of the PbPIFs gene family. The study examined protein physicochemical properties, gene structure, evolutionary relationships, subcellular localization, cis-acting elements in promoters, and expression patterns under light stress.
    Result Nine PbPIFs genes were identified from the P. bournei genome, all of which contained highly conserved bHLH domains as well as APA or APB domains. Subcellular localization revealed that PbPIFs proteins were exclusively localized in the nucleus. Promoter analysis showed that the upstream regions of PbPIFs harbored various cis-acting elements responsive to light, drought, low temperature, and hormones, with the highest number being ABA-responsive elements. Distince tissue-specific expression patterns were observed among PbPIFs family members. qPCR results showed that PbPIF1, PbPIF3a, PbPIF3b, and PbPIF5 were significantly downregulated under light induction, suggesting their involvement in photomorphogenesis.
    Conclusion The nine PbPIFs genes indentified in P.bournei exhibit functional diversification, with different members participating in responses to light signals and abiotic stressors. These findings provide a scientific basis for further dissecting the gene functions of PIF family members and their regulatory mechanisms in environmental responses.

     

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