Nopaline synthase: transcript mapping and DNA sequence.

A Depicker, S Stachel, P Dhaese, P Zambryski, H M Goodman
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Abstract

The DNA sequence of the nopaline synthase gene (nos) from Agrobacterium tumefaciens Ti plasmid pTiT37 and adjacent regions up to the right border of the T-DNA was determined. The 5' and 3' termini of the polyadenylated nos mRNA, isolated from a T37 tobacco teratoma tumor line, were localized by S1 mapping. The final mRNA is unspliced, encoded by a region of about 1450 bp, and specifies an open reading frame of 413 amino acids. Potential transcriptional signals in the 5' flanking DNA, such as CATAAA ("TATA box") and GGTCACTAT ("CAT box"), bear close resemblance to other eukaryotic promoters. Two putative polyadenylation signals, AATAAA and AATAAT, are found about 135 and 50 bp from the 3' end, respectively. This study may provide information for the development of expression vectors for genes in plant cells; moreover, the structural gene can be used as an easy screenable marker.

诺帕林合成酶:转录图谱和DNA序列。
测定了农杆菌Ti质粒pTiT37及其T-DNA右缘邻近区域的野碱合成酶基因(nos)的DNA序列。从T37烟草畸胎瘤细胞系中分离的多腺苷化nos mRNA的5'和3'端通过S1定位。最终的mRNA是未剪接的,由一个约1450 bp的区域编码,并指定一个由413个氨基酸组成的开放阅读框。5'侧DNA中的潜在转录信号,如CATAAA(“TATA盒”)和GGTCACTAT(“CAT盒”),与其他真核生物启动子非常相似。两个假定的聚腺苷化信号,AATAAA和AATAAT,分别在距离3'端135和50 bp处被发现。本研究可为植物细胞中基因表达载体的开发提供信息;此外,该结构基因可作为一种易于筛选的标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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