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Cloning of cDNA Sequences Encoding the Calcium-Binding Protein, Calmodulin, from Barley (Hordeum vulgare L.) 1

机译:大麦(Hordeum vulgare L.)1中编码钙结合蛋白钙调蛋白的cDNA序列的克隆

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摘要

Full- and partial-length cDNAs encoding calmodulin mRNA have been cloned and sequenced from barley (Hordeum vulgare L.). Barley leaf mRNA, size-fractionated in sucrose density gradients, was used to synthesize double-stranded cDNA. The cDNA was cloned in λgt10 and screened with a synthetic, 14-nucleotide oligonucleotide probe, which was designed using the predicted coding sequences of the carboxy termini of spinach and wheat calmodulin proteins. The primary structure of barley calmodulin, predicted from DNA sequencing experiments, consists of 148 amino acids and differs from that of wheat calmodulin in only three positions. In two of the three positions, the amino acid changes are conservative, while the third change consists of an apparent deletion/insertion. The overall nucleotide sequence similarity between the amino acid coding regions of barley and vertebrate calmodulin mRNAs is approximately 77%. However, a region encoding 11 amino acids of the second Ca2+-binding domain is very highly conserved at the nucleotide level compared with the rest of the coding sequences (94% sequence identity between barley and chicken calmodulin mRNAs). Genomic Southern blots reveal that barley calmodulin is encoded by a single copy gene. This gene is expressed as a single size class of mRNA in all tissues of 7-day-old barley seedlings. In addition, these analyses indicate that a barley calmodulin cDNA coding region subclone is suitable as a probe for isolating calmodulin genes from other plants.
机译:已经从大麦(大麦(Hordeum vulgare L.))克隆了编码钙调蛋白mRNA的全长和部分全长cDNA并对其进行了测序。用蔗糖密度梯度大小分级的大麦叶mRNA用于合成双链cDNA。将该cDNA克隆到λgt10中,并用合成的14个核苷酸的寡核苷酸探针进行筛选,该探针使用菠菜和小麦钙调蛋白蛋白的羧基末端的预测编码序列进行设计。 DNA测序实验预测,大麦钙调蛋白的一级结构由148个氨基酸组成,仅在三个位置与小麦钙调蛋白不同。在三个位置中的两个位置,氨基酸变化是保守的,而第三个变化由明显的缺失/插入组成。大麦和脊椎动物钙调蛋白mRNA的氨基酸编码区之间的总体核苷酸序列相似性约为77%。但是,与其余编码序列(大麦和鸡钙调蛋白mRNA之间的94%序列同一性)相比,第二个Ca2 +结合域的11个氨基酸编码区在核苷酸水平上非常保守。基因组Southern印迹显示大麦钙调蛋白由单拷贝基因编码。该基因在7日龄大麦幼苗的所有组织中均以单一大小的mRNA表达。另外,这些分析表明,大麦钙调蛋白cDNA编码区亚克隆适合作为从其他植物中分离钙调蛋白基因的探针。

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