She Q, Phan H, Garrett R A, Albers S V, Stedman K M, Zillig W
Institute of Molecular Biology, Copenhagen University, Denmark.
Extremophiles. 1998 Nov;2(4):417-25. doi: 10.1007/s007920050087.
The complete nucleotide sequence of the archaeal conjugative plasmid, pNOB8, from the Sulfolobus isolate NOB8-H2, was determined. The plasmid is 41,229 bp in size and contains about 50 ORFs. Several direct sequence repeats are present, the largest of which is a perfect 85-bp repeat and a site of intraplasmid recombination in foreign Sulfolobus hosts. This recombination event produces a major deletion variant, pNOB8-33, which is not stably maintained. Less than 20% of the ORFs could be assigned putative functions after extensive database searches. Tandem ORFs 315 and 470, within the deleted 8-kb region, show significant sequence similarity to the protein superfamilies of ParA (whole protein) and ParB (N-terminal half), respectively, that are important for plasmid and chromosome partitioning in bacteria. A putative cis-acting element is also present that exhibits six 24-mer repeats containing palindromic sequences which are separated by 39 or 42 bp. By analogy with bacterial systems, this element may confer plasmid incompatibility and define a group of incompatible plasmids in Archaea. Although several ORFs can form putative trans-membrane or membrane-binding segments, only two ORFs show significant sequence similarity to bacterial conjugative proteins. ORF630b aligns with the TrbE protein superfamily, which contributes to mating pair formation in Bacteria, while ORF1025 aligns with the TraG protein superfamily. We infer that the conjugative mechanism for Sulfolobus differs considerably from known bacterial mechanisms. Finally, two transposases were detected; ORF413 is flanked by an imperfect 32-bp inverted repeat with a 5-bp direct repeat at the ends, and ORF406 is very similar in sequence to an insertion element identified in the Sulfolobus solfataricus P2 genome.
测定了来自嗜酸热硫化叶菌分离株NOB8-H2的古菌接合质粒pNOB8的完整核苷酸序列。该质粒大小为41229 bp,包含约50个开放阅读框(ORF)。存在几个直接序列重复,其中最大的是一个85 bp的完美重复序列,也是在异源嗜酸热硫化叶菌宿主中质粒内重组的位点。这种重组事件产生了一个主要的缺失变体pNOB8-33,它不能稳定维持。经过广泛的数据库搜索后,不到20%的ORF可被赋予推定功能。缺失的8 kb区域内的串联ORF 315和470,分别与细菌中对质粒和染色体分配很重要的ParA(整个蛋白质)和ParB(N端一半)蛋白质超家族具有显著的序列相似性。还存在一个推定的顺式作用元件,它呈现出六个含有回文序列的24聚体重复,这些重复被39或42 bp隔开。与细菌系统类似,该元件可能赋予质粒不相容性,并在古菌中定义一组不相容质粒。尽管几个ORF可形成推定的跨膜或膜结合区段,但只有两个ORF与细菌接合蛋白具有显著的序列相似性。ORF630b与TrbE蛋白质超家族比对,该超家族有助于细菌中配对的形成,而ORF1025与TraG蛋白质超家族比对。我们推断嗜酸热硫化叶菌的接合机制与已知的细菌机制有很大不同。最后,检测到两个转座酶;ORF413两侧是一个不完美的32 bp反向重复,两端有一个5 bp的直接重复,并且ORF406在序列上与在嗜酸热栖热菌P2基因组中鉴定的一个插入元件非常相似。