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参与丝状噬菌体Cf16-v1新溶源插入到野油菜黄单胞菌柑橘致病变种染色体中的核苷酸序列。

Nucleotide sequences involved in the neolysogenic insertion of filamentous phage Cf16-v1 into the Xanthomonas campestris pv. citri chromosome.

作者信息

Dai H, Chow T Y, Liao H J, Chen Z Y, Chiang K S

机构信息

Institute of Botany, Academia Sinica, Taipei, Taiwan, ROC.

出版信息

Virology. 1988 Dec;167(2):613-20.

PMID:3201755
Abstract

Following a protracted carrier state in the infected cell, filamentous bacteriophage Cf16-v1 neolysogenizes Xanthomonas campestris pv. citri by inserting the phage genome into the host chromosome. The integration region in the phage and the host chromosome, respectively, and the two junctions in the lysogen chromosome were isolated and their nucleotide sequence was determined. The phage and host attachment sites shared an identical 15-bp "core," 5'-TATACATTATGCGAA-3'. Located on either side of each core were two unique arm sequences. Each of the two phage-host junctions contained an intact core flanked by a hybrid combination of phage and host arm sequences. A 10-bp symmetrical sequence arranged as inverted repeats with 1-bp spacing straddled the core sequence. A 10-bp repeated sequence, 5'-GCGCTATGGC-3', was found distal to the core in opposite orientation at the phage attachment site, while an abbreviated form of this sequence was present in the host attachment site. These sequence characteristics indicate that neolysogenic insertion of Cf16-v1 was accomplished by a site-specific recombination mechanism similar to lambda integration. However, in contrast to lambda, the phage and the host attachment sites in the Cf16-v1 system contained a high G + C nucleotide bias (except for the core sequence itself).

摘要

在感染细胞中经过一段漫长的携带状态后,丝状噬菌体Cf16-v1通过将噬菌体基因组插入宿主染色体,使柑橘溃疡病菌新溶源化。分别分离出噬菌体和宿主染色体中的整合区域以及溶源染色体中的两个连接点,并测定了它们的核苷酸序列。噬菌体和宿主的附着位点共享一个相同的15个碱基对的“核心”,即5'-TATACATTATGCGAA-3'。每个核心的两侧是两个独特的臂序列。两个噬菌体-宿主连接点中的每一个都包含一个完整的核心,两侧是噬菌体和宿主臂序列的混合组合。一个10个碱基对的对称序列以1个碱基对的间隔排列成反向重复,横跨核心序列。在噬菌体附着位点的核心远端发现了一个10个碱基对的重复序列,5'-GCGCTATGGC-3',其方向相反,而在宿主附着位点存在该序列的一个缩写形式。这些序列特征表明,Cf16-v1的新溶源插入是通过一种类似于λ整合的位点特异性重组机制完成的。然而,与λ不同的是,Cf16-v1系统中的噬菌体和宿主附着位点含有较高的G + C核苷酸偏差(核心序列本身除外)。

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