Department of Biology, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD 21218, USA.
J Bacteriol. 2010 Jul;192(14):3620-8. doi: 10.1128/JB.00154-10. Epub 2010 Apr 30.
Transfer of conjugative plasmids requires relaxases, proteins that cleave one plasmid strand sequence specifically. The F plasmid relaxase TraI (1,756 amino acids) is also a highly processive DNA helicase. The TraI relaxase activity is located within the N-terminal approximately 300 amino acids, while helicase motifs are located in the region comprising positions 990 to 1450. For efficient F transfer, the two activities must be physically linked. The two TraI activities are likely used in different stages of transfer; how the protein regulates the transition between activities is unknown. We examined TraI helicase single-stranded DNA (ssDNA) recognition to complement previous explorations of relaxase ssDNA binding. Here, we show that TraI helicase-associated ssDNA binding is independent of and located N-terminal to all helicase motifs. The helicase-associated site binds ssDNA oligonucleotides with nM-range equilibrium dissociation constants and some sequence specificity. Significantly, we observe an apparent strong negative cooperativity in ssDNA binding between relaxase and helicase-associated sites. We examined three TraI variants having 31-amino-acid insertions in or near the helicase-associated ssDNA binding site. B. A. Traxler and colleagues (J. Bacteriol. 188:6346-6353) showed that under certain conditions, these variants are released from a form of negative regulation, allowing them to facilitate transfer more efficiently than wild-type TraI. We find that these variants display both moderately reduced affinity for ssDNA by their helicase-associated binding sites and a significant reduction in the apparent negative cooperativity of binding, relative to wild-type TraI. These results suggest that the apparent negative cooperativity of binding to the two ssDNA binding sites of TraI serves a major regulatory function in F transfer.
转座子的转移需要松弛酶,这种蛋白质可以特异性地切割一条质粒链序列。F 质粒松弛酶 TraI(1756 个氨基酸)也是一种高效的 DNA 解旋酶。TraI 松弛酶活性位于 N 端约 300 个氨基酸内,而解旋酶基序位于包含位置 990 到 1450 的区域内。为了实现有效的 F 转移,这两种活性必须物理连接。这两种 TraI 活性可能在转移的不同阶段使用;该蛋白如何调节两种活性之间的转换尚不清楚。我们研究了 TraI 解旋酶单链 DNA(ssDNA)的识别,以补充之前对松弛酶 ssDNA 结合的探索。在这里,我们表明 TraI 解旋酶相关的 ssDNA 结合独立于并位于所有解旋酶基序的 N 端。与解旋酶相关的结合位点与 ssDNA 寡核苷酸具有纳摩尔级平衡解离常数和一些序列特异性结合。重要的是,我们观察到在松弛酶和与解旋酶相关的 ssDNA 结合位点之间的 ssDNA 结合中存在明显的强负协同作用。我们研究了三个在与解旋酶相关的 ssDNA 结合位点或附近具有 31 个氨基酸插入的 TraI 变体。B.A.Traxler 及其同事(J. Bacteriol. 188:6346-6353)表明,在某些条件下,这些变体从一种负调控形式中释放出来,使它们比野生型 TraI 更有效地促进转移。我们发现,与野生型 TraI 相比,这些变体的 ssDNA 通过其与解旋酶相关的结合位点的亲和力适度降低,并且结合的表观负协同性显著降低。这些结果表明,TraI 的两个 ssDNA 结合位点的结合的表观负协同性在 F 转移中起主要调节作用。