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首页> 外文期刊>Journal of the American Society for Horticultural Science >Cloning of the Self-incompatibility SFB Gene from Chinese Apricot 'Xiaobaixing' and Construction of the SFB Expression Vectors
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Cloning of the Self-incompatibility SFB Gene from Chinese Apricot 'Xiaobaixing' and Construction of the SFB Expression Vectors

机译:中国小杏杏自交不亲和SFB基因的克隆及SFB表达载体的构建

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摘要

Three kinds of expression vectors of a pollen-S determinant were constructed to provide a reference for molecular breeding of self-compatible (SC) Prunus species. An S-haplotype-specific F-box (SFB) protein gene from the 'Xiaobaixing' apricot (Prunus armeniaca) was cloned by reverse transcription polymerase chain reaction (RTPCR) and 3'-rapid-amplification of cDNA ends (3'-RACE). A 1136-bp sequence complementary to the 3'-end of the cDNA (GenBank accession number KP938528.2) with a 912-bp complete open reading frame (ORF) was obtained. The deduced amino acid sequence contained an F-box domain, two variable regions, and two hypervariable regions with structural characteristics similar to SFB in other Rosaceae plants. Sense, antisense, and RNA interference (RNAi) vectors for SFB were constructed by enzyme restriction. The target fragment was restricted using the corresponding restriction enzyme and then directionally inserted between the 35S cauliflower mosaic virus promoter and the nopaline synthase terminator (NOS-ter) of the expression vector pCAMBIA-35S-MCS-NOS-NPTII. The intron-containing hairpin RNA (ihpRNA) was obtained by fusion PCR. The constructed vectors were transferred into Agrobacterium tumefaciens strain LBA4404 by freezing/thawing. The RNAi vector of SFB was also transformed in tobacco (Nicotiana tabacum). The successful construction of these three expression vectors provides a basis for transforming 'Xiaobaixing' apricot and the breeding of SC Prunus cultivars.
机译:构建了花粉-S决定簇的三种表达载体,为自交(SC)李属物种的分子育种提供参考。通过逆转录聚合酶链反应(RTPCR)和cDNA末端的3'-快速扩增(3'-RACE)克隆了来自'小白杏'杏(Prunus armeniaca)的S-单倍型特异性F-box(SFB)蛋白基因。 )。获得与cDNA的3'-末端互补的1136-bp序列(GenBank登录号KP938528.2),具有912-bp的完全开放阅读框(ORF)。推导的氨基酸序列包含一个F-box结构域,两个可变区和两个高变区,其结构特征类似于其他蔷薇科植物中的SFB。通过酶切限制酶构建了SFB的有义,反义和RNA干扰(RNAi)载体。使用相应的限制酶限制目标片段,然后将其定向插入表达载体pCAMBIA-35S-MCS-NOS-NPTII的35S花椰菜花叶病毒启动子和胭脂碱合酶终止子(NOS-ter)之间。通过融合PCR获得含内含子的发夹RNA(ihpRNA)。通过冷冻/解冻将构建的载体转移至根癌农杆菌菌株LBA4404中。 SFB的RNAi载体也被转化到烟草(Nicotiana tabacum)中。这三种表达载体的成功构建,为小白杏的原核转化和李子李品种的选育奠定了基础。

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