Department of Microbiology-Immunology, Northwestern University's Feinberg School of Medicine, Chicago, IL, USA.
FEMS Microbiol Lett. 2012 Sep;334(1):44-8. doi: 10.1111/j.1574-6968.2012.02612.x. Epub 2012 Jul 3.
Natural transformation is the main means of horizontal genetic exchange in the obligate human pathogen Neisseria gonorrhoeae. Neisseria spp. have been shown to preferentially take up and transform their own DNA by recognizing a non-palindromic 10 or 12 nucleotide DNA uptake sequence (DUS10 or DUS12). We investigated the ability of the DUS12 to enhance single-stranded DNA (ssDNA) transformation. Given the non-palindromic nature of the DUS12, we tested whether both strands of the DUS equally enhance transformation. Recombinant single-stranded M13 phage harboring transforming DNA with the Watson DUS12, the Crick DUS12, or no DUS (DUS0) were constructed and circular ssDNA was purified. Southern blots of the purified DNA probed with strand-specific oligonucleotide probes showed > 10,000 : 1 ratio of ssDNA to contaminating dsDNA. The Crick strand of the DUS12 enhanced ssDNA transformation 180- to 470-fold over DUS0 ssDNA, whereas the Watson strand of the DUS only modestly enhanced ssDNA transformation in two strains of N. gonorrhoeae. These data confirm that ssDNA efficiently transforms N. gonorrhoeae, but that there is a strand preference and that part of this strand preference is a greater efficiency of the Crick strand of the DUS12 in enhancing transformation.
自然转化是专性人类病原体淋病奈瑟菌水平基因交换的主要途径。已经表明,奈瑟菌属优先通过识别非回文的 10 或 12 个核苷酸 DNA 摄取序列(DUS10 或 DUS12)来摄取和转化自身 DNA。我们研究了 DUS12 增强单链 DNA(ssDNA)转化的能力。鉴于 DUS12 的非回文性质,我们测试了 DUS 的两条链是否都能同等增强转化。构建了携带转化 DNA 的重组单链 M13 噬菌体,该 DNA 带有 Watson DUS12、Crick DUS12 或没有 DUS(DUS0),并纯化了环状 ssDNA。用链特异性寡核苷酸探针对纯化 DNA 的 Southern 印迹显示,ssDNA 与污染的 dsDNA 的比例> 10000:1。DUS12 的 Crick 链将 ssDNA 转化增强了 180-470 倍,而 DUS0 ssDNA 中 DUS12 的 Watson 链仅适度增强了两种淋病奈瑟菌菌株的 ssDNA 转化。这些数据证实,ssDNA 可以有效地转化淋病奈瑟菌,但存在链偏好,而这种链偏好的一部分是 DUS12 的 Crick 链在增强转化方面的更高效率。