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Q fever.Q热
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2
RNA splicing: group I intron crystal structures reveal the basis of splice site selection and metal ion catalysis.RNA剪接:I组内含子晶体结构揭示了剪接位点选择和金属离子催化的基础。
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Genetic diversity of the Q fever agent, Coxiella burnetii, assessed by microarray-based whole-genome comparisons.通过基于微阵列的全基因组比较评估Q热病原体贝纳柯克斯体的遗传多样性。
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Atomic level architecture of group I introns revealed.第一类内含子的原子水平结构得以揭示。
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Bacterial ribosomal RNA in pieces.细菌核糖体RNA片段化。
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Structure and assembly of group I introns.第一类内含子的结构与组装
Curr Opin Struct Biol. 2005 Jun;15(3):324-30. doi: 10.1016/j.sbi.2005.05.007.
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The natural history of group I introns.I类内含子的自然史。
Trends Genet. 2005 Feb;21(2):111-9. doi: 10.1016/j.tig.2004.12.007.
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The spread of LAGLIDADG homing endonuclease genes in rDNA.LAGLIDADG归巢内切酶基因在核糖体DNA中的传播。
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9
Active self-splicing group I introns in 23S rRNA genes of hyperthermophilic bacteria, derived from introns in eukaryotic organelles.嗜热细菌23S rRNA基因中的活性自我剪接I组内含子,源自真核细胞器中的内含子。
Proc Natl Acad Sci U S A. 2003 Sep 16;100(19):10806-11. doi: 10.1073/pnas.1434268100. Epub 2003 Aug 28.
10
Complete genome sequence of the Q-fever pathogen Coxiella burnetii.Q热病原体伯纳特柯克斯体的全基因组序列
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伯纳特柯克斯体异常的23S rRNA基因:两个自我剪接的I组内含子位于一个34个碱基对的外显子两侧,且其中一个元件缺乏典型的ωG。

The unusual 23S rRNA gene of Coxiella burnetii: two self-splicing group I introns flank a 34-base-pair exon, and one element lacks the canonical omegaG.

作者信息

Raghavan Rahul, Miller Scott R, Hicks Linda D, Minnick Michael F

机构信息

Division of Biological Sciences, The University of Montana, Missoula, MT 59812, USA.

出版信息

J Bacteriol. 2007 Sep;189(18):6572-9. doi: 10.1128/JB.00812-07. Epub 2007 Jul 20.

DOI:10.1128/JB.00812-07
PMID:17644584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2045182/
Abstract

We describe the presence and characteristics of two self-splicing group I introns in the sole 23S rRNA gene of Coxiella burnetii. The two group I introns, Cbu.L1917 and Cbu.L1951, are inserted at sites 1917 and 1951 (Escherichia coli numbering), respectively, in the 23S rRNA gene of C. burnetii. Both introns were found to be self-splicing in vivo and in vitro even though the terminal nucleotide of Cbu.L1917 is adenine and not the canonical conserved guanine, termed OmegaG, found in Cbu.L1951 and all other group I introns described to date. Predicted secondary structures for both introns were constructed and revealed that Cbu.L1917 and Cbu.L1951 were group IB2 and group IA3 introns, respectively. We analyzed strains belonging to eight genomic groups of C. burnetii to determine sequence variation and the presence or absence of the elements and found both introns to be highly conserved (>/=99%) among them. Although phylogenetic analysis did not identify the specific identities of donors, it indicates that the introns were likely acquired independently; Cbu.L1917 was acquired from other bacteria like Thermotoga subterranea and Cbu.L1951 from lower eukaryotes like Acanthamoeba castellanii. We also confirmed the fragmented nature of mature 23S rRNA in C. burnetii due to the presence of an intervening sequence. The presence of three selfish elements in C. burnetii's 23S rRNA gene is very unusual for an obligate intracellular bacterium and suggests a recent shift to its current lifestyle from a previous niche with greater opportunities for lateral gene transfer.

摘要

我们描述了伯氏考克斯氏体唯一的23S rRNA基因中两个自我剪接的I组内含子的存在及其特征。这两个I组内含子,即Cbu.L1917和Cbu.L1951,分别插入到伯氏考克斯氏体23S rRNA基因的第1917位和第1951位(以大肠杆菌的编号为准)。尽管Cbu.L1917的末端核苷酸是腺嘌呤,而非Cbu.L1951以及迄今描述的所有其他I组内含子中发现的典型保守鸟嘌呤(称为OmegaG),但发现这两个内含子在体内和体外均能自我剪接。构建了这两个内含子的预测二级结构,结果显示Cbu.L1917和Cbu.L1951分别为IB2组和IA3组内含子。我们分析了属于伯氏考克斯氏体八个基因组群的菌株,以确定序列变异以及元件的存在与否,结果发现这两个内含子在它们之间高度保守(≥99%)。尽管系统发育分析未确定供体的具体身份,但表明这些内含子可能是独立获得的;Cbu.L1917是从其他细菌如地下嗜热栖热菌获得的,而Cbu.L1951是从低等真核生物如卡氏棘阿米巴获得的。我们还证实了由于存在间隔序列,伯氏考克斯氏体中成熟23S rRNA具有片段化的性质。伯氏考克斯氏体23S rRNA基因中存在三种自私元件,这对于专性细胞内细菌来说是非常不寻常的,表明其最近从先前具有更多横向基因转移机会的生态位转变为当前的生活方式。