1School of Life Sciences, Pharmacy, and Chemistry, Kingston University, Penrhyn Road, Kingston upon Thames, KT1 2EE, UK.
2Department of Pharmacology, University of Illinois at Chicago, Chicago, Illinois, USA.
Microb Genom. 2016 Aug 25;2(8):e000069. doi: 10.1099/mgen.0.000069. eCollection 2016 Aug.
DNA uptake sequences are widespread throughout the genome. These short, conserved sequences facilitate the exchange of endogenous DNA between members of the genus . Often the DNA uptake sequences are present as inverted repeats that are able to form hairpin structures. It has been suggested previously that DNA uptake sequence inverted repeats present 3' of genes play a role in -independent termination and attenuation. However, there is conflicting experimental evidence to support this role. The aim of this study was to determine the role of DNA uptake sequences in transcriptional termination. Both bioinformatics predictions, conducted using TransTermHP, and experimental evidence, from RNA-seq data, were used to determine which inverted repeat DNA uptake sequences are transcriptional terminators and in which direction. Here we show that DNA uptake sequences in the inverted repeat configuration occur in both where the DNA uptake sequence precedes the inverted version of the sequence and also, albeit less frequently, in reverse order. Due to their symmetrical configuration, inverted repeat DNA uptake sequences can potentially act as bi-directional terminators, therefore affecting transcription on both DNA strands. This work also provides evidence that gaps in DNA uptake sequence density in the gonococcal genome coincide with areas of DNA that are foreign in origin, such as prophage. This study differentiates for the first time, to our knowledge, between DNA uptake sequences that form intrinsic transcriptional terminators and those that do not, providing characteristic features within the flanking inverted repeat that can be identified.
DNA 摄取序列广泛存在于基因组中。这些短的、保守的序列促进了属内成员之间内源性 DNA 的交换。通常,DNA 摄取序列以能够形成发夹结构的反向重复存在。先前有人提出,位于基因 3'端的 DNA 摄取序列反向重复在非依赖性终止和衰减中起作用。然而,有相互矛盾的实验证据来支持这一作用。本研究旨在确定 DNA 摄取序列在转录终止中的作用。使用 TransTermHP 进行的生物信息学预测和来自 RNA-seq 数据的实验证据都被用来确定哪些反向重复 DNA 摄取序列是转录终止子,以及它们的方向。在这里,我们表明,在反向重复配置中的 DNA 摄取序列既出现在 DNA 摄取序列在序列的反向版本之前的位置,也出现在反向顺序的位置,尽管频率较低。由于它们的对称结构,反向重复 DNA 摄取序列可以作为双向终止子,因此会影响两条 DNA 链上的转录。这项工作还提供了证据表明,淋球菌基因组中 DNA 摄取序列密度的间隙与起源于外源的 DNA 区域(如噬菌体)相吻合。这项研究首次区分了形成内在转录终止子的 DNA 摄取序列和不形成的 DNA 摄取序列,提供了可以识别的侧翼反向重复中的特征。