农杆菌Ti质粒编码章鱼碱合成酶基因的核苷酸序列和转录图谱。

H De Greve, P Dhaese, J Seurinck, M Lemmers, M Van Montagu, J Schell
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引用次数: 0

摘要

我们已经确定了冠胆酶,章鱼碱合成酶基因的完整核苷酸序列。该序列来源于农杆菌Ti质粒Ach5的克隆片段。它显示了一个连续的开放阅读框,编码358个氨基酸的多肽链。利用S1核酸酶作图技术,测定了烟草肿瘤细胞系成熟章鱼氨酸合成酶mRNA 5′端和多聚(A)添加位点对应的核苷酸位置。在基因组DNA侧翼鉴定出两个与真核基因转录控制区非常相似的序列:序列5'- tatttaa -3'位于转录起始位点上游32个碱基对处,序列5'-AATAAT-3'位于poly(a)加成位点前方17个碱基对处。未翻译的5'先导序列中不存在Shine-Dalgarno序列。观察结果表明,该DNA序列虽然自然由细菌质粒携带,但被编程为功能性植物基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleotide sequence and transcript map of the Agrobacterium tumefaciens Ti plasmid-encoded octopine synthase gene.

We have determined the complete nucleotide sequence of the gene for the crown gall enzyme, octopine synthase. The sequence was derived from cloned fragments of the Agrobacterium tumefaciens Ti plasmid Ach5. It displayed a continuous open reading frame encoding a polypeptide chain of 358 amino acids. The nucleotide positions corresponding to the 5' end and poly(A) addition site of the mature octopine synthase mRNA from a tobacco tumor cell line were determined by S1 nuclease mapping. Two sequences closely resembling transcriptional control regions found in eukaryotic genes transcribed by RNA polymerase II were identified in the flanking genomic DNA: a sequence 5'-TATTTAAA-3' was located 32 base pairs upstream from the initiation site of transcription, and a hexanucleotide 5'-AATAAT-3' occurred 17 base pairs in front of the poly(A) addition site. No Shine-Dalgarno sequence was present in the untranslated 5' leader sequence. The observations indicate that this DNA sequence, although naturally carried by a bacterial plasmid, is programmed as a functional plant gene.

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