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根癌土壤杆菌pTiC58的virB操纵子编码11个开放阅读框。

The virB operon of Agrobacterium tumefaciens pTiC58 encodes 11 open reading frames.

作者信息

Kuldau G A, De Vos G, Owen J, McCaffrey G, Zambryski P

机构信息

Department of Plant Biology, University of California, Berkeley 94720.

出版信息

Mol Gen Genet. 1990 Apr;221(2):256-66. doi: 10.1007/BF00261729.

Abstract

Agrobacterium tumefaciens genetically transforms plant cells by transferring a copy of its T-DNA to the plant where it is integrated and stably maintained. In the presence of wounded plant cells this process is activated and mediated by the products of the vir genes which are grouped into six distinct loci. The largest is the virB locus spanning 9.5 kb. Transposon mutagenesis studies have shown that virB gene products are required for virulence but their functions remain largely unknown. To provide information relevant to understanding the function of VirB polypeptides, the nucleotide sequence of the virB operon from a nopaline plasmid, pTiC58, is presented here. Eleven open reading frames (ORFs) are predicted from this sequence. The predicted sizes of 10 of the 11 VirB polypeptides are verified by specific expression in Escherichia coli. Only the product of the smallest ORF potentially encoding a 5.8 kDa polypeptide has not been detected. The initiation of translation of five virB ORFs occurs at codons that overlap the termination codons of the ORF immediately upstream; thus, translational coupling may be an important mechanism for efficient translation of the large virB polycistronic mRNA. Based on hydropathy plot analysis nine of the virB ORFs encode proteins that may interact with membranes; these data support the earlier hypothesis that virB gene products may form a membrane pore or channel to mediate exit of the T-DNA copy (T-strands) from Agrobacterium into the plant cell. A comparison of the two published octopine virB sequences with the nopaline sequence presented here is made.

摘要

根癌土壤杆菌通过将其T-DNA的一个拷贝转移到植物细胞中并使其整合和稳定维持来对植物细胞进行遗传转化。在受伤的植物细胞存在的情况下,这个过程由vir基因的产物激活并介导,这些基因被分为六个不同的位点。最大的是跨越9.5 kb的virB位点。转座子诱变研究表明,virB基因产物是毒力所必需的,但其功能在很大程度上仍然未知。为了提供与理解VirB多肽功能相关的信息,这里展示了来自胭脂碱型质粒pTiC58的virB操纵子的核苷酸序列。从这个序列预测出11个开放阅读框(ORF)。11个VirB多肽中有10个的预测大小通过在大肠杆菌中的特异性表达得到了验证。只有最小的ORF(可能编码一个5.8 kDa的多肽)的产物未被检测到。5个virB ORF的翻译起始发生在与紧邻上游ORF的终止密码子重叠的密码子处;因此,翻译偶联可能是大的virB多顺反子mRNA高效翻译的一个重要机制。基于亲水性图谱分析,9个virB ORF编码可能与膜相互作用的蛋白质;这些数据支持了早期的假设,即virB基因产物可能形成一个膜孔或通道,以介导T-DNA拷贝(T链)从土壤杆菌进入植物细胞。这里还对已发表的两个章鱼碱型virB序列与本文展示的胭脂碱型序列进行了比较。

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