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来自绿色产色链霉菌Tü494的膦丝菌素N-乙酰转移酶基因的核苷酸序列及其在烟草中的表达。

Nucleotide sequence of the phosphinothricin N-acetyltransferase gene from Streptomyces viridochromogenes Tü494 and its expression in Nicotiana tabacum.

作者信息

Wohlleben W, Arnold W, Broer I, Hillemann D, Strauch E, Pühler A

机构信息

Lehrstuhl für Genetik, Fakultät für Biologie, Universität Bielefeld, F.R.G.

出版信息

Gene. 1988 Oct 15;70(1):25-37. doi: 10.1016/0378-1119(88)90101-1.

DOI:10.1016/0378-1119(88)90101-1
PMID:3240868
Abstract

The phosphinothricin (Pt) N-acetyltransferase gene (pat) of Streptomyces viridochromogenes Tü494 is located on a 0.8-kb BglII fragment [Strauch et al., Gene 63 (1988) 65-74]. By sequencing a 1.3-kb BglII-SstII fragment, an open reading frame representing the pat gene was found. It encodes a polypeptide of 183 amino acids with an Mr of 20,621. The base composition of the pat gene is typical for Streptomyces [70.1 mol% (G + C) in total and 93.5 mol% (G + C) in the third position]. Translation of pat is initiated by a GTG codon which was identified by frameshift mutations in Escherichia coli as well as in Streptomyces lividans. Significant homology of the pat gene was found to the bialaphos-resistance gene (bar) of Streptomyces hygroscopicus [Thompson et al., EMBO J. 9 (1987) 2519-2523]. However, variations were detected in the 5'-noncoding region of the two resistance genes which may reflect differences in regulation. Since Pt is a potent herbicide, the pat gene was modified and introduced into Nicotiana tabacum by Agrobacterium-mediated leaf-disc transformation. The GTG start codon of pat was replaced by ATG. Subsequently the modified pat-coding region was fused to the 35S promoter of the cauliflower mosaic virus. Transgenic plants could directly be selected on Pt-containing medium.

摘要

绿色产色链霉菌Tü494的膦丝菌素(Pt)N - 乙酰转移酶基因(pat)位于一个0.8 kb的BglII片段上[施特劳赫等人,《基因》63(1988)65 - 74]。通过对一个1.3 kb的BglII - SstII片段进行测序,发现了一个代表pat基因的开放阅读框。它编码一个由183个氨基酸组成的多肽,分子量为20,621。pat基因的碱基组成是链霉菌的典型特征[总共70.1摩尔%(G + C),第三位为93.5摩尔%(G + C)]。pat的翻译由一个GTG密码子起始,该密码子通过大肠杆菌和变铅青链霉菌中的移码突变得以鉴定。发现pat基因与吸水链霉菌的双丙氨磷抗性基因(bar)有显著同源性[汤普森等人,《欧洲分子生物学组织杂志》9(1987)2519 - 2523]。然而,在两个抗性基因的5'非编码区检测到了差异,这可能反映了调控上的差异。由于Pt是一种强效除草剂,对pat基因进行了修饰,并通过农杆菌介导的叶盘转化法将其导入烟草。pat的GTG起始密码子被ATG取代。随后,将修饰后的pat编码区与花椰菜花叶病毒的35S启动子融合。转基因植物可以直接在含Pt的培养基上进行筛选。

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