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首页> 外文期刊>Journal of Experimental Botany >ZmbZIP91 regulates expression of starch synthesis-related genes by binding to ACTCAT elements in their promoters
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ZmbZIP91 regulates expression of starch synthesis-related genes by binding to ACTCAT elements in their promoters

机译:ZmbZIP91通过与启动子中的ACTCAT元件结合来调节淀粉合成相关基因的表达

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摘要

Starch synthesis is a key process that influences crop yield and quality, though little is known about the regulation of this complex metabolic pathway. Here, we present the identification of ZmbZIP91 as a candidate regulator of starch synthesis via co-expression analysis in maize (Zea mays L.). ZmbZIP91 was strongly associated with the expression of starch synthesis genes. Reverse tanscription-PCR(RT-PCR) and RNA in situ hybridization indicated that ZmbZIP91 is highly expressed in maize endosperm, with less expression in leaves. Particle bombardment- mediated transient expression in maize endosperm and leaf protoplasts demonstrated that ZmbZIP91 could positively regulate the expression of starch synthesis genes in both leaves and endosperm. Additionally, the Arabidopsis mutant vip1 carried a mutation in a gene (VIP1) that is homologous to ZmbZIP91, displayed altered growth with less starch in leaves, and ZmbZIP91 was able to complement this phenotype, resulting in normal starch synthesis. A yeast one-hybrid experiment and EMSAs showed that ZmbZIP91 could directly bind to ACTCAT elements in the promoters of starch synthesis genes (pAGPS1, pSSI, pSSIIIa, and pISA1). These results demonstrate that ZmbZIP91 acts as a core regulatory factor in starch synthesis by binding to ACTCAT elements in the promoters of starch synthesis genes.
机译:淀粉合成是影响作物产量和品质的关键过程,尽管对该复杂代谢途径的调控知之甚少。在这里,我们通过玉米(Zea mays L.)中的共表达分析鉴定ZmbZIP91作为淀粉合成的候选调节剂。 ZmbZIP91与淀粉合成基因的表达密切相关。反转录-PCR(RT-PCR)和RNA原位杂交表明ZmbZIP91在玉米胚乳中高表达,在叶片中表达少。粒子轰击介导的玉米胚乳和叶片原生质体瞬时表达表明,ZmbZIP91可以正向调节叶片和胚乳中淀粉合成基因的表达。此外,拟南芥突变体vip1在一个与ZmbZIP91同源的基因(VIP1)中携带一个突变,显示出生长变化,叶片中的淀粉更少,ZmbZIP91能够补充该表型,从而导致正常的淀粉合成。酵母单杂交实验和EMSA表明,ZmbZIP91可以直接与淀粉合成基因(pAGPS1,pSSI,pSSIIIa和pISA1)启动子中的ACTCAT元件结合。这些结果表明,ZmbZIP91通过与淀粉合成基因启动子中的ACTCAT元件结合而充当淀粉合成中的核心调控因子。

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