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本文引用的文献

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Mechanism of antigenic variation in Mycoplasma pulmonis: interwoven, site-specific DNA inversions.肺炎支原体抗原变异机制:交织的位点特异性DNA倒位
Mol Microbiol. 1995 Nov;18(4):703-14. doi: 10.1111/j.1365-2958.1995.mmi_18040703.x.
2
Generation of Campylobacter fetus S-layer protein diversity utilizes a single promoter on an invertible DNA segment.胎儿弯曲杆菌S层蛋白多样性的产生利用了一个位于可逆DNA片段上的单一启动子。
Mol Microbiol. 1996 Mar;19(6):1241-53. doi: 10.1111/j.1365-2958.1996.tb02469.x.
3
Pathogenesis of Campylobacter fetus infections: critical role of high-molecular-weight S-layer proteins in virulence.胎儿弯曲杆菌感染的发病机制:高分子量S层蛋白在毒力中的关键作用。
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Rearrangement of sapA homologs with conserved and variable regions in Campylobacter fetus.胎儿弯曲杆菌中具有保守和可变区域的sapA同源物的重排。
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7265-9. doi: 10.1073/pnas.90.15.7265.
5
A lipopolysaccharide-binding domain of the Campylobacter fetus S-layer protein resides within the conserved N terminus of a family of silent and divergent homologs.胎儿弯曲杆菌S层蛋白的脂多糖结合结构域位于一组沉默且不同源的同源物保守N端内。
J Bacteriol. 1995 Apr;177(7):1734-41. doi: 10.1128/jb.177.7.1734-1741.1995.
6
High-frequency S-layer protein variation in Campylobacter fetus revealed by sapA mutagenesis.通过sapA诱变揭示胎儿弯曲杆菌高频S层蛋白变异
Mol Microbiol. 1994 Nov;14(3):453-62. doi: 10.1111/j.1365-2958.1994.tb02180.x.
7
Segmental conservation of sapA sequences in type B Campylobacter fetus cells.胎儿弯曲杆菌B型细胞中sapA序列的片段保守性。
J Biol Chem. 1995 Jun 23;270(25):15093-101. doi: 10.1074/jbc.270.25.15093.
8
Protein shift and antigenic variation in the S-layer of Campylobacter fetus subsp. venerealis during bovine infection accompanied by genomic rearrangement of sapA homologs.胎儿弯曲杆菌性病亚种在牛感染期间S层中的蛋白质迁移和抗原变异,伴有sapA同源物的基因组重排。
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Shift in S-layer protein expression responsible for antigenic variation in Campylobacter fetus.负责胎儿弯曲杆菌抗原变异的S层蛋白表达变化。
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A site-specific, conservative recombination system carried by bacteriophage P1. Mapping the recombinase gene cin and the cross-over sites cix for the inversion of the C segment.由噬菌体P1携带的位点特异性保守重组系统。绘制重组酶基因cin和C片段倒位的交叉位点cix图谱。
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嵌套式DNA倒位作为程序性基因重排的范例

Nested DNA inversion as a paradigm of programmed gene rearrangement.

作者信息

Dworkin J, Blaser M J

机构信息

Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Feb 4;94(3):985-90. doi: 10.1073/pnas.94.3.985.

DOI:10.1073/pnas.94.3.985
PMID:9023369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC19626/
Abstract

Programmed gene rearrangements are employed by a variety of microorganisms, including viruses, prokaryotes, and simple eukaryotes, to control gene expression. In most instances in which organisms mediate host evasion by large families of homologous gene cassettes, the mechanism of variation is not thought to involve DNA inversion. Here we report that Campylobacter fetus, a pathogenic Gram-negative bacterium, reassorts a single promoter, controlling surface-layer protein expression, and one or more complete ORFs strictly by DNA inversion. Rearrangements were independent of the distance between sites of inversion. These rearrangements permit variation in protein expression from the large surface-layer protein gene family and suggest an expanding paradigm of programmed DNA rearrangements among microorganisms.

摘要

多种微生物,包括病毒、原核生物和简单的真核生物,利用程序性基因重排来控制基因表达。在大多数情况下,生物体通过大量同源基因盒介导宿主逃避,其变异机制被认为不涉及DNA倒位。在此我们报告,胎儿弯曲杆菌,一种致病性革兰氏阴性菌,通过DNA倒位严格地重新排列单个启动子(控制表层蛋白表达)以及一个或多个完整的开放阅读框。重排与倒位位点之间的距离无关。这些重排允许来自大的表层蛋白基因家族的蛋白质表达发生变异,并提示微生物中程序性DNA重排的模式正在扩展。