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来自胭脂碱型质粒pTiC58的VirD2基因产物具有毒力所需的至少两种活性。

VirD2 gene product from the nopaline plasmid pTiC58 has at least two activities required for virulence.

作者信息

Steck T R, Lin T S, Kado C I

机构信息

Department of Plant Pathology, University of California, Davis 95616.

出版信息

Nucleic Acids Res. 1990 Dec 11;18(23):6953-8. doi: 10.1093/nar/18.23.6953.

Abstract

Virulence genes virD1 and virD2 are required for T-DNA processing in Agrobacterium tumefaciens. The regions within virD2 contributing to T-DNA processing and virulence were investigated. Some insertional mutations in virD2 prevented T-DNA border endonucleolytic cleavage and produced an avirulent phenotype. However, a non-polar insertion immediately after bp 684 of the 1344 bp open reading frame of virD2 did not inhibit endonucleolytic cleavage but still caused a loss of virulence. This suggested that in addition to T-DNA border cleaving activity, the VirD2 protein has another virulence function which resides in the C-terminal half of the protein. Comparative nucleotide sequence analyses of virD2 showed that the first 684 bp were 81% homologous to virD2 of an octopine Ti plasmid whereas the remaining 660 bp were only 44% homologous. A plasmid containing the virD region from octopine Ti plasmid could restore both virulence and processing to a nopaline virD2 mutant. No complementation resulted when a nopaline virD2 clone containing a region similar to eukaryotic nuclear envelope transport sequences was deleted from the 3' end. These results suggest that virD1 and only the first half of virD2 are required to encode for the T-DNA processing endonuclease, and that the 3'-half of virD2 encodes a function separate from endonuclease activity that is required for virulence.

摘要

毒性基因virD1和virD2是根癌土壤杆菌中T-DNA加工所必需的。研究了virD2中对T-DNA加工和毒性有贡献的区域。virD2中的一些插入突变阻止了T-DNA边界内切核酸酶切割,并产生了无毒表型。然而,在virD2的1344 bp开放阅读框的684 bp之后立即发生的非极性插入并不抑制内切核酸酶切割,但仍然导致毒性丧失。这表明,除了T-DNA边界切割活性外,VirD2蛋白还具有另一种毒性功能,该功能存在于该蛋白的C端一半中。virD2的比较核苷酸序列分析表明,前684 bp与章鱼碱Ti质粒的virD2有81%的同源性,而其余660 bp只有44%的同源性。一个含有来自章鱼碱Ti质粒的virD区域的质粒可以恢复胭脂碱virD2突变体的毒性和加工能力。当从3'端删除一个含有与真核细胞核膜转运序列相似区域的胭脂碱virD2克隆时,没有产生互补作用。这些结果表明,virD1和仅virD2的前半部分是编码T-DNA加工内切核酸酶所必需的,并且virD2的3'端一半编码一种与毒性所需的内切核酸酶活性分开的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95eb/332755/c0001297035a/nar00207-0205-a.jpg

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