Atmakuri Krishnamohan, Cascales Eric, Burton Oliver T, Banta Lois M, Christie Peter J
Department of Microbiology and Molecular Genetics, University of Texas Medical School at Houston, Houston, TX 77030, USA.
EMBO J. 2007 May 16;26(10):2540-51. doi: 10.1038/sj.emboj.7601696.
Agrobacterium tumefaciens translocates T-DNA through a polar VirB/D4 type IV secretion (T4S) system. VirC1, a factor required for efficient T-DNA transfer, bears a deviant Walker A and other sequence motifs characteristic of ParA and MinD ATPases. Here, we show that VirC1 promotes conjugative T-DNA transfer by stimulating generation of multiple copies per cell of the T-DNA substrate (T-complex) through pairwise interactions with the processing factors VirD2 relaxase, VirC2, and VirD1. VirC1 also associates with the polar membrane and recruits T-complexes to cell poles, the site of VirB/D4 T4S machine assembly. VirC1 Walker A mutations abrogate T-complex generation and polar recruitment, whereas the native protein recruits T-complexes to cell poles independently of other polar processing factors (VirC2, VirD1) or T4S components (VirD4 substrate receptor, VirB channel subunits). We propose that A. tumefaciens has appropriated a progenitor ParA/MinD-like ATPase to promote conjugative DNA transfer by: (i) nucleating relaxosome assembly at oriT-like T-DNA border sequences and (ii) spatially positioning the transfer intermediate at the cell pole to coordinate substrate-T4S channel docking.
根癌土壤杆菌通过极性VirB/D4 IV型分泌(T4S)系统转运T-DNA。VirC1是高效T-DNA转移所需的一个因子,具有异常的沃克A基序以及ParA和MinD ATP酶特有的其他序列基序。在此,我们表明,VirC1通过与加工因子VirD2解旋酶、VirC2和VirD1进行成对相互作用,刺激每个细胞产生多个T-DNA底物拷贝(T复合体),从而促进接合性T-DNA转移。VirC1还与极性膜结合,并将T复合体招募到细胞两极,即VirB/D4 T4S机器组装的位点。VirC1的沃克A突变消除了T复合体的产生和极性招募,而天然蛋白独立于其他极性加工因子(VirC2、VirD1)或T4S组分(VirD4底物受体、VirB通道亚基)将T复合体招募到细胞两极。我们提出,根癌土壤杆菌已利用一种祖先的ParA/MinD样ATP酶,通过以下方式促进接合性DNA转移:(i)在类oriT的T-DNA边界序列处形成松弛体组装核心,以及(ii)在细胞两极对转移中间体进行空间定位,以协调底物与T4S通道的对接。