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LaPCBER1基因在'Tresor'百合鳞茎发育过程中的功能解析OA

Functional Analysis of LaPCBER1 Gene During the Development of Bulbs of Lilium'Tresor'

中文摘要英文摘要

[目的]分析苯基香豆满苄基醚还原酶基因LaPCBER1在'Tresor'百合鳞茎发育过程中的表达模式,并探究其对百合鳞茎膨大的影响以及在此过程中对木质素含量的调控作用。[方法]基于'Tresor'百合鳞茎膨大过程的转录组数据,筛选到 1 个注释为PCBER1 的差异基因,以'Tresor'百合鳞茎cDNA为模板克隆LaPCBER1基因,并利用生物信息学软件分析其编码蛋白的理化性质;通过荧光定量PCR(qRT-PCR)检测LaPCBER1 在百合不同组织及不同发育时期的表达模式;利用病毒诱导的基因沉默(VIGS)和瞬时过表达技术探究其对鳞茎膨大的影响,并利用试剂盒检测不同时期以及过表达LaPCBER1 后百合鳞茎的木质素含量。[结果]LaPCBER1 的DNA序列全长为 930 bp,编码 309 个氨基酸,共预测到51个磷酸化位点,编码蛋白为非跨膜且不稳定亲水性蛋白。qRT-PCR结果显示,LaPCBER1 在茎中表达量最高,在鳞茎发育S4 时期(快速膨大期)表达量达峰值。瞬时过表达LaPCBER1 后,转基因鳞茎木质素含量较空载体对照提高 49.7%,鲜质量、干质量及直径相对增长率分别提高 29.0%、29.7%和 37.2 %;而沉默LaPCBER1后,鳞茎鲜质量、干质量及直径相对增长率分别降低 35.9%、38.7%和 32.2 %,木质素含量降低 24.3%。[结论]LaPCBER1 基因在鳞茎发育早期高表达,且能促进木质素积累与鳞茎膨大,推测LaPCBER1参与'Tresor'百合鳞茎的膨大过程,并在该过程中发挥正向调控作用。

[Objective]To analyze the expression pattern of the phenylcoumaran benzylic ether reductase gene LaPCBER1 during bulb development in Lilium'Tresor',and to investigate its effects on bulb enlargement as well as its role in regulating lignin content during this process.[Method]By analyzing transcriptomic data from the bulb enlargement process of Lilium'Tresor',a differentially expressed gene annotated as PCBER1 was screened.The LaPCBER1 gene was cloned using cDNA from Lilium'Tresor'bulbs as the template,and the physicochemical properties of the encoded protein were analyze using bioinformatics software.The expression patterns of LaPCBER1 in different tissues and different developmental stages of Lilium'Tresor'were detected by quantitative real-time PCR(qRT-PCR).The effects of LaPCBER1 on bulb enlargement were investigated using transient overexpression techniques,and the lignin content of lily bulbs at different stages and following overexpression was measured using assay kits.[Result]The full-length DNA sequenceof LaPCBER1 is 930 bp,encoding 309 amino acids.The protein is predicted to have 51 phosphorylation sites and is characterized as a non-transmembrane,unstable,hydrophilic protein.qRT-PCR results showed that LaPCBER1 was highly expressed in the stem,with expression peaking during the S4 stage(rapid expansion stage)of bulb development.Following transient overexpression of LaPCBER1,the lignin content in transgenic bulbs increased by 49.7% compared to the vector.The fresh weight,dry weight,and relative growth rates of circumference of the bulbs increased by 29.0%,29.7%,and 37.2%,respectively;Conversely,after silencing LaPCBER1,the fresh weight,dry weight,and relative growth rates of circumference of the bulbs decreased by 35.9%,38.7%,and 32.2%,respectively,and the lignin content decreased by 24.3%.[Conclusion]Expression pattern and functional analysis of LaPCBER1 suggest that this gene is highly expressed during the early stages of bulb development and promotes lignin accumulation and bulb expansion.It is therefore hypothesized that LaPCBER1 is involved in the bulb expansion process of Lilium'Tresor'and plays a positive regulatory role in this process.

金梦竹;王梦迪;陈妍竹;马艳芳;李青源;康伟丽;潘文强;于晓南;杜运鹏

北京林业大学园林学院,北京 100083||北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097北京林业大学园林学院,北京 100083||北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097北京林业大学园林学院,北京 100083||北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097北京林业大学园林学院,北京 100083||北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097||福建农林大学风景园林与艺术学院,福建 福州 350100北京市延庆区种苗花卉产业服务站,北京 102100北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097北京林业大学园林学院,北京 100083北京市农林科学院草业花卉与景观生态研究所/百合国家林业和草原局重点实验室,北京 100097

农业科技

'Tresor'百合LaPCBER1 基因鳞茎膨大木质素表达分析功能分析

Lilium'Tresor'LaPCBER1 genebulbs expansionligninexpression analysisfunctional analysis

《广东农业科学》 2026 (2)

67-79,13

国家重点研发计划项目(2024YFD1600902)北京市农林科学院科技创新能力建设专项(2026-2027)北京市农林科学院优秀青年基金(YKPY2026017)北京市农林科学院优秀青年科学家培养计划项目(YXQN202303-C)

10.16768/j.issn.1004-874X.2026.02.005

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