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为了获得光皮树脂肪酸去饱和酶合成的关键基因，本研究以光皮树未成熟种子为材料克隆FAD7基因，并利用qPCR技术分析果实发育过程中FAD7基因表达量变化。结果表明：光皮树FAD7基因(SwFA D7)编码区长1800 bp，推测编码448个氨基酸，相对分子质量51.29 kD，等电点7.14，具有三个跨膜结构域。SwFA D7基因所编码的蛋白质含有FAD蛋白家族所特有四个富含组氨酸的保守区域。SwFAD7蛋白的二级结构组要由α-螺旋和无规则卷曲构成，蛋白质中均夹杂分布着β-折叠。系统进化树分析表明SwFA D7单独形成一个分支。对未成熟果实中SwFA D7基因表达分析表明，该基因在7~8月间呈现先上升后下降再上升的表达变化趋势，于7月23日左右达到累积的最高点。“,”In order to obtain the key gene in linolenic acid formation way in cornus wilsoniana, the immature fruits were used to clone FAD7 gene, and qPCR technology was used to analyze the FAD7 gene expression changes in the process of fruit development . FAD7 gene ( named SwFA D7 ) was cloned from cornus wilsoniana using RACE strategy. The cDNA of SwFA D7 is 1 800 bp in length which presumably code 448 amino acids. Its MW (molecular weight) is 51.29 kD with the isoelectric point 7.14, and it has three across membrane structure. The protein coded by SwFA D7 gene contains the unique four conservative histidine-rich regions which is an important feature in FAD gene family. Theα-helixs and random coils are the main structural components of its secondary structure, whileβ-sheets spread in the whole protein. The phylogenetic tree analysis showed that the genetic relationship of SwFA D7 is separated as an independent branch. The result of SwFA D7 gene expression in immature fruit showed that the gene expression present as increase-decrease-increase pattern from July to August, with the highest point at July 23.