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Repeated extragenic sequences in prokaryotic genomes: a proposal for the origin and dynamics of the RUP element in Streptococcus pneumoniae

机译:原核基因组中重复的泛症序列:肺炎链球菌肺炎链球菌中RUP元素的起源和动态的提案

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A survey of all Streptococcus pneumoniae GenBank/EMBL DNA sequence entries and of the public domain sequence (representing more than 90% of the genome) of an S. pneumoniae type 4 strain allowed identification of 108 copies of a 107-bp-long highly repeated intergenic element called RUP (for repeat unit of pneumococcus). Several features of the element, revealed in this study, led to the proposal that RUP is an insertion sequence (IS)-derivative that could still be mobile. Among these features are: (1) a highly significant homology between the terminal inverted repeats (IRs) of RUPs and of IS630-Spn1, a new putative IS of S. pneumoniae; and (2) insertion at a TA dinucleotide, a characteristic target of several members of the IS630 family. Trans-mobilization of RUP is therefore proposed to be mediated by the transposase of IS630-Spn1. To account for the observation that RUPs are distributed among four subtypes which exhibit different degrees of sequence homogeneity, a scenario is invoked based on successive stages of RUP mobility and non-mobility, depending on whether an active transposase is present or absent. In the latter situation, an active transposase could be reintroduced into the species through natural transformation. Examination of sequences flanking RUP revealed a preferential association with ISs. It also provided evidence that RUPs promote sequence rearrangements, thereby contributing to genome flexibility. The possibility that RUP preferentially targets transforming DNA of foreign origin and subsequently favours disruption/rearrangement of exogenous sequences is discussed.
机译:对所有链球菌肺炎群岛GeNBank / Embl DNA序列条目的调查和S.肺炎型4型菌株的公共领域序列(基因组的90%)允许鉴定为107-BP长重复的108份代表性元素称为RUP(用于肺炎球菌的重复单位)。在本研究中揭示了该元素的几个特征,导致RUP是仍然是移动的插入序列(是)的插入序列(是)。这些特征是:(1)RUP的末端倒置重复(IS630-SPN1的终端倒置重复(IRS)之间具有高度显着的同源性,这是S.肺炎的新推定; (2)插入Ta二核苷酸,是IS630家族的几个成员的特征目标。因此,提出了通过IS630-SPN1的转座酶介导的RUP的跨动力化。为了考虑观察结果,RUP分布在表现出不同程度的序列均匀度的四个亚型中,根据有效转座酶是否存在或不存在,基于RUP移动性和非移动性的连续阶段来调用场景。在后一种情况下,可以通过天然转化重新介绍活性转座酶。检查序列侧翼RUP揭示了与ISS的优先关系。它还提供了Rups促进序列重排的证据,从而有助于基因组灵活性。讨论了RUP优先靶向异物转化的DNA,随后讨论了外源序列的破坏/重新排列。

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