Redfield Rosemary J, Findlay Wendy A, Bossé Janine, Kroll J Simon, Cameron Andrew D S, Nash John He
Dept. of Zoology, University of British Columbia, Vancouver, BC, Canada.
BMC Evol Biol. 2006 Oct 12;6:82. doi: 10.1186/1471-2148-6-82.
Many bacteria can take up DNA, but the evolutionary history and function of natural competence and transformation remain obscure. The sporadic distribution of competence suggests it is frequently lost and/or gained, but this has not been examined in an explicitly phylogenetic context. Additional insight may come from the sequence specificity of uptake by species such as Haemophilus influenzae, where a 9 bp uptake signal sequence (USS) repeat is both highly overrepresented in the genome and needed for efficient DNA uptake. We used the distribution of competence genes and DNA uptake specificity in H. influenzae's family, the Pasteurellaceae, to examine the ancestry of competence.
A phylogeny of the Pasteurellaceae based on 12 protein coding genes from species with sequenced genomes shows two strongly supported subclades: the Hin subclade (H. influenzae, Actinobacillus actinomycetemcomitans, Pasteurella multocida, Mannheimia succiniciproducens, and H. somnus), and the Apl subclade (A. pleuropneumoniae, M. haemolytica, and H. ducreyi). All species contained homologues of all known H. influenzae competence genes, consistent with an ancestral origin of competence. Competence gene defects were identified in three species (H. somnus, H. ducreyi and M. haemolytica); each appeared to be of recent origin. The assumption that USS arise by mutation rather than copying was first confirmed using alignments of H. influenzae proteins with distant homologues. Abundant USS-like repeats were found in all eight Pasteurellacean genomes; the repeat consensuses of species in the Hin subclade were identical to that of H. influenzae (AAGTGCGGT), whereas members of the Apl subclade shared the consensus ACAAGCGGT. All species' USSs had the strong consensus and flanking AT-rich repeats of H. influenzae USSs. DNA uptake and competition experiments demonstrated that the Apl-type repeat is a true USS distinct from the Hin-type USS: A. pleuropneumoniae preferentially takes up DNA fragments containing the Apl-type USS over both H. influenzae and unrelated DNAs, and H. influenzae prefers its own USS over the Apl type.
Competence and DNA uptake specificity are ancestral properties of the Pasteurellaceae, with divergent USSs and uptake specificity distinguishing only the two major subclades. The conservation of most competence genes over the approximately 350 million year history of the family suggests that lineages that lose competence may be evolutionary dead ends.
许多细菌能够摄取DNA,但自然感受态和转化的进化历史及功能仍不清楚。感受态的零星分布表明其经常丢失和/或获得,但尚未在明确的系统发育背景下进行研究。更多的见解可能来自于如流感嗜血杆菌等物种摄取的序列特异性,其中一个9bp的摄取信号序列(USS)重复在基因组中高度富集,并且是高效摄取DNA所必需的。我们利用流感嗜血杆菌所属的巴斯德菌科中感受态基因的分布和DNA摄取特异性来研究感受态的起源。
基于来自已测序基因组物种的12个蛋白质编码基因构建的巴斯德菌科系统发育树显示出两个得到有力支持的亚分支:Hin亚分支(流感嗜血杆菌、伴放线放线杆菌、多杀巴斯德菌、产琥珀酸曼氏杆菌和睡眠嗜血杆菌)和Apl亚分支(胸膜肺炎放线杆菌、溶血曼氏杆菌和杜氏嗜血杆菌)。所有物种都含有所有已知流感嗜血杆菌感受态基因的同源物,这与感受态的祖先起源一致。在三个物种(睡眠嗜血杆菌、杜氏嗜血杆菌和溶血曼氏杆菌)中发现了感受态基因缺陷;每个缺陷似乎都是近期出现的。通过将流感嗜血杆菌蛋白质与远缘同源物进行比对,首次证实了USS是由突变而非复制产生的这一假设。在所有八个巴斯德菌科基因组中都发现了丰富的类似USS的重复序列;Hin亚分支中物种的重复序列共有序列与流感嗜血杆菌的相同(AAGTGCGGT),而Apl亚分支的成员共享共有序列ACAAGCGGT。所有物种的USS都具有流感嗜血杆菌USS的强共有序列和富含AT的侧翼重复序列。DNA摄取和竞争实验表明,Apl型重复序列是一种与Hin型USS不同的真正的USS:胸膜肺炎放线杆菌优先摄取含有Apl型USS的DNA片段,而不是流感嗜血杆菌和无关的DNA,流感嗜血杆菌则优先摄取其自身的USS而非Apl型。
感受态和DNA摄取特异性是巴斯德菌科的祖先特性,不同的USS和摄取特异性仅区分两个主要亚分支。在该科约3.5亿年的历史中,大多数感受态基因得以保留,这表明失去感受态的谱系可能是进化的死胡同。