Hilse R, Hammerschmidt S, Bautsch W, Frosch M
Institut für Medizinische Mikrobiologie, Medizinische Hochschule, Hannover, Germany.
J Bacteriol. 1996 May;178(9):2527-32. doi: 10.1128/jb.178.9.2527-2532.1996.
The insertion element IS1301 has been shown to mediate capsule phase variation in Neisseria meningitidis found in N. serogroup B by reversible insertional inactivation of the siaA gene. We have determined the target site specificity of this element by cloning and sequencing the insertion sites of 12 identical IS1301 copies found in N. meningitidis B1940. A target consensus core of 5'-AYTAG-3' was identified, with the central TA being duplicated following insertion. Additional features around the target sites, including extended palindromic symmetry, stem-loop formation, and the high incidence of AT tracts, indicate that other factors, such as DNA secondary structure, are involved in target recognition. The left inverted repeat of an IS1016-like element acts as a hot spot for insertion, with one insertion element combination located upstream of their gene. According to further sequence analysis, we were able to place IS1301 in the IS5 subgroup within the IS4 family of elements. A survey of 135 Neisseria strains indicated the presence of IS1301 in 27.9 to 33.3% of N. meningitides serogroup B, C, and W135 strains and in 86.7% of serogroup Y strains. IS1301 did not occur in serogroup A strains, in Neisseria gonorrhoeae, or in apathogenic Neisseria spp.
插入元件IS1301已被证明可通过siaA基因的可逆插入失活介导B群脑膜炎奈瑟菌的荚膜相变。我们通过克隆和测序在脑膜炎奈瑟菌B1940中发现的12个相同IS1301拷贝的插入位点,确定了该元件的靶位点特异性。鉴定出一个5'-AYTAG-3'的靶标共有核心序列,插入后中央TA会重复。靶位点周围的其他特征,包括扩展的回文对称性、茎环形成和富含AT序列,表明其他因素,如DNA二级结构,也参与了靶标识别。一个类IS1016元件的左反向重复序列是插入热点,有一个插入元件组合位于其基因上游。根据进一步的序列分析,我们能够将IS1301置于IS4元件家族的IS5亚组中。对135株奈瑟菌的调查表明,在27.9%至33.3%的B、C和W135群脑膜炎奈瑟菌菌株以及86.7%的Y群菌株中存在IS1301。A群菌株、淋病奈瑟菌或无致病性奈瑟菌属中未出现IS1301。