石榴木质素合成相关基因PgMYB308的克隆和表达分析
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国家自然科学基金(30900971)


Cloning and Expression Analysis of Lignin BiosynthesisRelated Gene PgMYB308 in Pomegranate
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    摘要:

    该研究以‘红玉石籽’ (Punica granatum cv. Hongyushizi)石榴为试验材料,采用RACE和RTPCR方法,获得与木质素的合成相关基因PgMYB308PgMYB308基因cDNA全长792 bp,编码263个氨基酸。分子量为29.56 kD,理论等电点为9.07。序列比对和功能域分析发现,PgMYB308包含R2和R3保守域, 以及C1、C2、C4和锌指基序。系统进化树分析显示,PgMYB308与其他物种起源相同,而与桉树EgMYB308亲缘关系最近。荧光定量PCR分析表明,PgMYB308在茎、叶和种子等组织中均有表达,其中茎中表达量最高,叶片中表达量最低;PgMYB308在‘突尼斯软籽’中表达最高,而在‘红玉石籽’和‘白玉石籽’中表达量较低;PgMYB308在‘红玉石籽’籽粒的不同时期均有表达,但在花后20 d相对表达量最高,以后随发育进程呈现逐渐下降的趋势。

    Abstract:

    In this study, PgMYB308,the related gene to the synthesis of lignin, was cloned using RACE and RTPCR methods, with ‘Punica granatum cv. Hongyushizi’ as the experimental materials. The cDNA fulllength sequence of PgMYB308 was 792 bp, which reduced 263 amino acids. Sequence alignment and functional domain analysis revealed that PgMYB308 contained R2, R3, C1, C2, C4 and Zing finger motifs. Phylogenetic tree analysis indicated that PgMYB308 shared the same origin with other species, and had the closest relationship with Eucalyptus grandis EgMYB308. The fluorescent quantitative PCR analysis showed that PgMYB308 expression was detected in stems, leaves and seeds. The expression in stems were the highest, while the lowest in leaves; PgMYB308 expression was higher in ‘Tunisiruanzi’, while lower in ‘Hongyushizi’ and ‘Baiyushizi’; PgMYB308 expression was detected in ‘Hongyushizi’ seeds of different periods. The relative expression of PgMYB308 gradually declined from 20 d to -120 d, and the relative expression was the highest at 20 d.

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黄 蓉,熊 枫,陈 磊,等.石榴木质素合成相关基因PgMYB308的克隆和表达分析[J].西北植物学报,2017,37(12):2357-2362

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  • 在线发布日期: 2017-12-29
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