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首页> 外文期刊>Molecular biology reports >Instability of short-sequence DNA repeats of pear pathogenic Erwinia strains from Japan and Erwinia amylovora fruit tree and raspberry strains.
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Instability of short-sequence DNA repeats of pear pathogenic Erwinia strains from Japan and Erwinia amylovora fruit tree and raspberry strains.

机译:来自日本的梨病原性欧文氏杆菌菌株和支链淀粉欧文氏果树和覆盆子菌株的短序列DNA重复序列不稳定。

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摘要

An array of short-sequence DNA repeats (SSRs) occurs in the plasmid pEA29 of the fire blight pathogen Erwinia amylovora. A large number of "fruit tree" strains, mainly from Central and Western Europe, were screened for their SSR numbers, and the analyses were extended to five raspberry strains from North America and six pear pathogenic Erwinia strains from Japan. The repeat ATTACAGA present in all E. amylovorastrains was found to be reiterated 3 to 15 times. The Japanese strains contained the major repeat sequence GGATTCTG, which was reiterated 16 to 24 times. ATTACAGG, which resembles the SSR of E. amylovora, was reiterated two or three times. In a novel approach, sequencing gels were used to visualize the rare occurrence of shorter arrays (down to three repeats) in E. amylovoraand the Japanese Erwinia strains. Changes in the repeat numbers in E. amylovora were observed repeatedly when the bacteria had been exposed to stress conditions. The repeat structures of homo- and heteroduplices of PCR-amplified repeats were also analyzed by cleavage of annealed molecules with the single-strand-specific endonuclease from bacteriophage T4. Not only heteroduplexes, but also homoduplexes showed non-matching regions in the SSRs, which could arise from transient formation of loops due to strand slippage during the assays.
机译:在火疫病病原体解淀粉欧文氏菌(Erwinia amylovora)的质粒pEA29中出现了一系列短序列DNA重复序列(SSR)。筛选了主要来自中欧和西欧的大量“果树”菌株的SSR编号,并将分析扩展到了来自北美的五种覆盆子菌株和来自日本的六种梨致病性欧文氏菌菌株。发现存在于所有淀粉链球菌菌株中的重复ATTACAGA重复了3至15次。日本菌株含有主要重复序列GGATTCTG,其重复16至24次。重复了两到三遍,类似于大肠埃希氏菌的SSR的ATTACAGG。在一种新颖的方法中,测序凝胶被用于可视化在支链球菌和日本欧文氏菌菌株中较短阵列(少至三个重复)的罕见情况。当细菌暴露于压力条件下时,可反复观察到支链淀粉中重复数的变化。还通过用来自噬菌体T4的单链特异性核酸内切酶切割退火的分子来分析PCR扩增的重复序列的同二聚体和异二聚体的重复结构。不仅异源双链体,而且同质双链体均显示出SSR中的不匹配区域,这可能是由于测定过程中链滑移而导致的环的瞬时形成所致。

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