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作 者:沈丙权[1] 郑贝贝[1] 彭慧芳[1] 郭天财[1] 康国章[1]
机构地区:[1]河南农业大学国家小麦工程技术研究中心,郑州450002
出 处:《西北农业学报》2010年第7期61-65,共5页Acta Agriculturae Boreali-occidentalis Sinica
基 金:国家自然科学基金(30871472);国家转基因专项子课题(082102140020-003和2009ZX08002-21B);作物生物学国家重点实验室开放课题(2009KF01)
摘 要:利用RT-PCR方法从普通玉米浚单20中克隆出淀粉合成关键酶-腺苷二磷酸葡萄糖焦磷酸化酶(ADP-Glucose Pyrophosphorylase,AGPase)胞质型小亚基(cytosolic small subunit,SSUI)基因的cDNA序列,命名为ZmSSUI(GenBank登录号:GU550073)。序列分析表明,该cDNA序列长度1554 bp,包含一个完整的开放阅读框(2~1 429 bp),长度为1 428 bp,编码476个氨基酸,克隆基因编码的氨基酸序列与其他植物SSUI氨基酸序列有较高同源性。半定量RT-PCR分析表明,在籽粒发育过程中,ZmSSUI基因的表达呈单峰状变化,与已报道的AGPase酶活性及淀粉积累速率趋势基本一致,推测其在玉米淀粉合成中发挥着重要作用。A cDNA sequence encoding a cytosolic small subunit gene of AGPase was isolated from maize(Zea mays) by RT-PCR and designated as ZmSSU I(GenBank Accession No.GU550073).Its length was 1 554 bp,containing an open reading frame(ORF) of 1 428 bp encoding a putative protein of 476 amino acids.Sequence alignment indicated that the putative amino acid sequence of ZmSSU I shared high identities 96%,94%,91% and 89% to Zea mays(AAN39299),Sorghum bicolor(ABK97531),Oryza sativa(ACJ86322) and Triticum aestivum(AAF61173),respectively.The transcription levels of ZmSSU I in maize kernels were analyzed with semi-quantitative RT-PCR method.Results showed that the expression of ZmSSU I in developing kernels had a single-peak curve occurring 30 d after pollination.The results showed that ZmSSU I played an important role in maize starch biosynthesis.
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