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Molecular cloning and characterization of a cDNA encoding endonuclease from potato (Solanum tuberosum)

机译:马铃薯(Solanum tuberosum)编码核酸内切酶的cDNA的分子克隆和鉴定

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摘要

A cDNA, StEN1, encoding a potato (Solanum tuberosum) endonuclease was cloned and sequenced. The nucleotide sequence of this clone contains an open reading frame of 906 nucleotides encoding a protein of 302 amino acids, and with a calculated molecular mass of 34.4kDa and a Pi of 5.6. The deduced StEN1 protein contains a putative signal sequence of 25 amino acid residues. The StEN1 encoded protein shows substantial homology to both plant and fungal endonucleases isolated and cloned from other sources. The highest identity (73%) was observed with AgCEL I from celery, Apium graveolens, ZEN1 from Zinnia elegans (69%) and DSA6 from daylily, Hemerocallis (68%). RT-PCR expression analysis demonstrated that the potato StEN1 gene is constitutively expressed in potato, although minor differences in expression level in different tissues were observed.
机译:克隆并测序了编码马铃薯(Solanum tuberosum)核酸内切酶的cDNA StEN1。该克隆的核苷酸序列包含一个906个核苷酸的开放阅读框,编码302个氨基酸的蛋白质,计算的分子量为34.4kDa,Pi为5.6。推导的StEN1蛋白包含25个氨基酸残基的推定信号序列。 StEN1编码的蛋白质与从其他来源分离和克隆的植物和真菌核酸内切酶均显示出实质同源性。芹菜中的AgCEL I,重症芹菜中的AgCEL I,百日草(Zinnia elegans)中的ZEN1(69%)和黄花菜萱草(萱草)的DSA6(68%)观察到最高的身份。 RT-PCR表达分析表明马铃薯StEN1基因在马铃薯中组成性表达,尽管观察到在不同组织中表达水平的微小差异。

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