玉米FAD2基因的克隆与序列分析。

植物生理与分子生物学学报 Pub Date : 2006-12-01
Fang Tao, Su-Wen Zhu, Jun Fan, Bei-Jiu Cheng
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引用次数: 0

摘要

在植物中,δ -12去饱和酶参与了油酸转化为亚油酸的过程。利用其他高等植物中已发表的δ -12去饱和酶基因的保守寡氨基酸残基,利用逆转录聚合酶链反应(RT-PCR)从未成熟玉米胚的总RNA中扩增出cDNA片段。根据cDNA序列的生物信息分析,利用RT-PCR技术从玉米未成熟胚中分离出FAD2基因的一个特异性片段,并从玉米基因组中扩增出相同长度的DNA。序列分析结果表明,它们的长度均为1 164 bp,只有一个编码387个氨基酸的开放阅读框(ORF),且在FAD2 ORF中不含内含子(GenBank登录DQ496227)。克隆FAD2的氨基酸序列与其他植物δ -12脂肪酸去饱和酶的氨基酸序列具有较高的一致性。它包含三个组氨酸基序和两个长链疏水残基,表明一个完整的膜蛋白跨越膜四次。半定量RT-PCR分析表明,FAD2在玉米幼胚中的表达强于在叶片、茎和根中的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning and sequence analysis of maize FAD2 gene.

Delta-12 desaturases are involved in the conversion of oleic acid to linoleic acid in plant. Based on the conserved oligo amino acid residues of the published delta-12 desaturase genes from other higher plant species, a cDNA fragment was amplified by RT-PCR (reverse transcriptase-polymerase chain reaction) from the total RNA of immature maize embryos. According to bioinformation analysis of the cDNA sequence, a specific fragment of FAD2 gene was isolated by RT-PCR from immature maize embryos, and DNA of the same length was amplified from maize genome. Results of sequence analysis indicate that they are all 1 164 bp long, and have just an open reading frame (ORF) coding for 387 amino acids, and there is no intron in the FAD2 ORF (GenBank accession DQ496227). The deduced amino acid sequence of the cloned FAD2 showed high identity to those of other plant delta-12 fatty acid desaturases. It contains three histidine motifs and two long stretches of hydrophobic residues, indicative of an integral membrane protein spanning membrane four times. Analysis by semi-quantitive RT-PCR showed that FAD2 was strongly expressed in maize immature embryos than in leaves, stems and roots.

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