Hosking Sarah L, Deadman Mary E, Moxon E Richard, Peden John F, Saunders Nigel J, High Nicola J
University of Manchester, School of Biological Sciences1.800, Stopford Building, Oxford Road, Manchester M13 9PTUK.
Molecular Infectious Diseases Group, University of Oxford, Institute of Molecular MedicineJohn Radcliffe Hospital, Headington, Oxford OX3 9DSUK.
Microbiology (Reading). 1998 Sep;144 ( Pt 9):2525-2530. doi: 10.1099/00221287-144-9-2525.
The transposon Tn916 was evaluated as a tool for generalized mutagenesis of the genome of Haemophilus influenzae. This was achieved in silico by searching the genome sequence of H. influenzae Rd for the published Tn916 target site consensus sequence 5' TT/ATTTT(N)6AAAAAA/TA. This search identified 16 putative target sites. In subsequent experiments, integration of Tn916 did not occur at any of these sites. Using the nucleotide sequences of these observed integration sites, a new consensus sequence, 5' TTTTT(N)xAAAAA (4 < or = x < or = 7), was derived. This sequence reflects the curve-twist-curve DNA topology which is a feature common to all Tn916 integration sites. A search of the H. influenzae Rd genome using the new consensus sequence identified 167 potential target sites, representing approximately 1% of the total genome. Only 80 of these sites were located within ORFs. The presence of such a limited number of target sites places severe constraints on the use of Tn916 as a tool for generalized mutagenesis of the genome of H. influenzae.
转座子Tn916被评估作为流感嗜血杆菌基因组普遍诱变的一种工具。这是通过在计算机上搜索流感嗜血杆菌Rd的基因组序列,寻找已发表的Tn916靶位点共有序列5' TT/ATTTT(N)6AAAAAA/TA来实现的。该搜索鉴定出16个假定的靶位点。在随后的实验中,Tn916并未在这些位点中的任何一个发生整合。利用这些观察到的整合位点的核苷酸序列,推导得到一个新的共有序列5' TTTTT(N)xAAAAA (4 ≤ x ≤ 7)。该序列反映了曲线-扭曲-曲线DNA拓扑结构,这是所有Tn916整合位点共有的特征。使用新的共有序列搜索流感嗜血杆菌Rd基因组,鉴定出167个潜在靶位点,约占基因组总数的1%。其中只有80个位点位于开放阅读框内。如此有限数量的靶位点的存在,严重限制了Tn916作为流感嗜血杆菌基因组普遍诱变工具的应用。