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滇牡丹油体蛋白基因的克隆、表达及功能的初步分析OA

Cloning,Expression,and Preliminary Functional Analysis of Oleosin Gene in Paeonia delavayi

中文摘要英文摘要

油体蛋白(oleosin,OLE)在植物的油脂合成和储存过程中发挥关键作用,本研究以滇牡丹(Paeonia delavayi)为材料,对PdOLE进行基因克隆、生物信息学分析、表达模式分析及亚细胞定位分析等研究,旨在初步阐明该基因在滇牡丹油脂合成中发挥的作用.结果表明,PdOLE 基因(GenBank No.PX564745)序列全长411 bp,可编码136个氨基酸.生物信息学分析表明,该蛋白包含1个OLE超家族结构域及13个磷酸化位点,无信号肽,且二级和三级结构中α-螺旋占比最高.序列比对结果表明,PdOLE蛋白序列与近缘物种'凤丹'牡丹(P.ostii)、芍药(P.lactiflora)OLE蛋白的同源性较低,而与可可(Theobroma cacao)、油橄榄(Olea europaea)、芝麻(Sesamum indicum)和向日葵(Helianthus annuus)4种油料作物的同源性较高,系统进化树结果进一步表明,PdOLE蛋白与上述近缘物种中OLE蛋白的亲缘关系较远,与上述4种油料作物的亲缘关系较近.qRT-PCR结果表明,在滇牡丹种子中的PdOLE基因表达水平显著高于其他器官(P<0.05),且在90 DPF(day post flowers)时达到最高表达量.滇牡丹种子石蜡切片的尼罗红染色观察结果表明,种子中的脂滴数量在发育中期(60 DPF后)呈现显著增加,可以较好地解释PdOLE基因的表达趋势.亚细胞定位结果表明PdOLE蛋白定位于细胞膜.本研究为进一步解析OLE基因功能及滇牡丹油脂合成规律提供了科学依据.

Oleosin(OLE)plays a crucial role in the synthesis and storage of plant oils.Using Paeonia delavayi as the experimental material,this study conducted gene cloning,bioinformatics analysis,expression pattern analysis,and subcellular localization analysis to initially clarify the possible role of PdOLE gene in the oil synthesis of P.delavayi.The results showed that the PdOLE gene(GenBank No.PX564745)sequence was 411 bp in length and could encode 136 amino acids.Bioinformatics analysis indicated that the protein contained an OLE superfamily domain and 13 phosphorylation sites,lacked a signal peptide,and exhibited the highest proportion of α-helix in its secondary and tertiary structures.Sequence alignment results showed that the PdOLE protein had relatively low identity with OLE homologs from the closely related species P.ostii and P.lactiflora.Notably,it showed significantly higher homology with OLE proteins derived from 4 representative oil crops:Theobroma cacao,Olea europaea,Sesamum indicum,and Helianthus annuus.Consistent with the results,phylogenetic tree construction further demonstrated that the PdOLE protein formed distinct clade separated from the OLE proteins of the closely related species mentioned above,and clustered more closely with those from the selected oil crops,indicating a closer evolutionary affinity.The qRT-PCR results indicated that the expression level of the PdOLE gene in seeds was significantly higher than that in other organs(P<0.05),reaching its peak at 90 DPF(day post flowers).Nile red staining of paraffin sections demonstrated that the number of seed lipid droplet increased significantly at mid-development(after 60 DPF),accounting well for the PdOLE expression trend.Subcellular localization results indicated that the PdOLE protein was localized to the cell membrane.This study would provide a scientific basis for future investigations aimed at elucidating OLE gene function and the oil biosynthesis pathway of P.delavayi.

邱维维;李红艳;陈静蕾;李欣如;王娟;张鹏远

西南林业大学 生物与食品工程学院,昆明 650224西南林业大学 生物与食品工程学院,昆明 650224西南林业大学 生物与食品工程学院,昆明 650224西南林业大学 生物与食品工程学院,昆明 650224西南林业大学 林学院,昆明 650224西南林业大学 生物与食品工程学院,昆明 650224

农业科技

滇牡丹油体蛋白基因(OLE)基因克隆表达模式分析亚细胞定位

Paeonia delavayiOleosin gene(OLE)Gene cloningExpression pattern analysisSubcellular localization

《农业生物技术学报》 2026 (5)

1076-1088,13

国家自然科学基金(32060089)云南省基础研究计划(202401AT070296)

10.3969/j.issn.1674-7968.2026.05.013

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