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首页> 外文期刊>Genes & Genetic Systems >Cloning and characterization of two full-length cDNAs, TaGA1 and TaGA2, encoding G-protein alpha subunits expressed differentially in wheat genome
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Cloning and characterization of two full-length cDNAs, TaGA1 and TaGA2, encoding G-protein alpha subunits expressed differentially in wheat genome

机译:小麦基因组中差异表达的编码G蛋白α亚基的两个全长cDNA TaGA1和TaGA2的克隆与鉴定

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In the present study, we identified and characterized two cDNAs, named TaGA1 and TaGA2, encoding alpha subunits of heterotrimeric G proteins synthesized from one-week-old seedling mRNAs of common wheat cv. S615 using RACE PCR and RT-PCR methods. The clone TaGA1 contained an open reading frame that encoded a protein consisting of 383 amino acid residues with a molecular mass of 51.3 kDa, whereas the clone TaGA2 contained an open reading frame encoding 390 amino acids with a molecular mass of 52.5 kDa. At the amino acid level, both cDNAs (TaGA1 and TaGA2) showed 70-96% and 30-40% homologies to plant and animal G-protein alpha (G a) subunits, respectively, and 97.7% homology to each other. The regions essential for binding to GTP were conserved among all G alpha subunits in higher plants and mammals examined. However, the C-terminal amino acid sequences of TaGA1 and TaGA2 were similar to those of cereal G alpha subunits (rice and barley) but were different from the analogous sequences of mammalian G alpha subunits as well as from those of the leguminous and Solanaeceous G alpha subunits. Southern analysis revealed that the hexaploid wheat genome contained three major copies of G alpha subunit gene with a few less homologous copies. The analysis of the expression for G alpha subunit genes in wheat showed that both TaGA1 and TaGA2 mRNAs were abundant in one-week-old seedlings, immature seeds harvested one-week after anthesis, young spikes and internodes, indicating constitutive expression patterns in all of the organs tested. Especially, young spikes and internodes exhibited increased levels of mRNA accumulation, suggesting that G alpha subunit gene is highly expressed in actively elongating and fast growing tissues. Moreover, both TaGA1 and TaGA2 showed genome-specific expressions in wheat and may participate in the light-regulated growth and development of the seedlings.
机译:在本研究中,我们鉴定并鉴定了两个cDNA,分别称为TaGA1和TaGA2,它们编码从普通小麦cv的一周龄幼苗mRNA合成的异三聚体G蛋白的α亚基。 S615使用RACE PCR和RT-PCR方法。 TaGA1克隆包含一个开放阅读框,其编码由383个氨基酸残基组成的蛋白质,分子量为51.3 kDa,而TaGA2克隆包含一个开放阅读框,编码390个氨基酸,分子量为52.5 kDa。在氨基酸水平上,两个cDNA(TaGA1和TaGA2)分别与植物和动物G蛋白α(G a)亚基的同源性为70-96%和30-40%,彼此具有97.7%的同源性。在所研究的高等植物和哺乳动物中,与GTP结合所必需的区域在所有G alpha亚基中均保守。但是,TaGA1和TaGA2的C末端氨基酸序列与谷类Gα亚基(大米和大麦)相似,但与哺乳动物Gα亚基的相似序列以及豆科和豆科G的相似。 alpha亚基。 Southern分析表明,六倍体小麦基因组包含三个主要拷贝的Gα亚基基因,而具有较少的同源拷贝。对小麦中G alpha亚基基因表达的分析表明,TaGA1和TaGA2 mRNA在一周龄的幼苗中均丰富,花后一周收获的未成熟种子,幼穗和节间,表明在所有玉米中本构表达模式。被测器官特别是,年轻的穗状花序和节间表现出增加的mRNA积累水平,这表明Gα亚基基因在活跃的伸长和快速生长的组织中高度表达。此外,TaGA1和TaGA2在小麦中均显示了基因组特异性表达,并且可能参与了光调节的幼苗生长和发育。

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