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Tracking EcoKI and DNA fifty years on: a golden story full of surprises

机译:追踪EcoKI和DNA五十年:充满惊喜的金色故事

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1953 was a historical year for biology, as it marked the birth of the DNA helix, but also a report by Bertani and Weigle on 'a barrier to infection' of bacteriophage λ in its natural host, Escherichia coli K-12, that could be lifted by 'host-controlled variation' of the virus. This paper lay dormant till Nobel laureate Arber and PhD student Dussoix showed that the λ DNA was rejected and degraded upon infection of different bacterial hosts, unless it carried host-specific modification of that DNA, thus laying the foundations for the phenomenon of restriction and modification (R-M). The restriction enzyme of E.coli K-12, EcoKI, was purified in 1968 and required S-adenosylmethionine (AdoMet) and ATP as cofactors. By the end of the decade there was substantial evidence for a chromosomal locus hsdK with three genes encoding restriction (R), modification (M) and specificity (S) subunits that assembled into a large complex of >400 kDa. The 1970s brought the message that EcoKI cut away from its DNA recognition target, to which site the enzyme remained bound while translocating the DNA past itself, with concomitant ATP hydrolysis and subsequent double-strand nicks. This translocation event created clearly visible DNA loops in the electron microscope. EcoKI became the archetypal Type I R-M enzyme with curious DNA translocating properties reminiscent of helicases, recognizing the bipartite asymmetric site AAC(N6)GTGC. Cloning of the hsdK locus in 1976 facilitated molecular understanding of this sophisticated R-M complex and in an elegant 'pas de deux' Murray and Dryden constructed the present model based on a large body of experimental data plus bioinformatics. This review celebrates the golden anniversary of EcoKI and ends with the exciting progress on the vital issue of restriction alleviation after DNA damage, also first reported in 1953, which involves intricate control of R subunit activity by the bacterial proteasome ClpXP, important results that will keep scientists on the EcoKI track for another 50 years to come.
机译:1953年是生物学史上具有历史意义的一年,因为它标志着DNA螺旋的诞生,同时也是Bertani和Weigle报道的天然宿主大肠杆菌K-12中噬菌体λ的“感染障碍”。由病毒的“宿主控制的变异”解除。这篇论文一直处于休眠状态,直到诺贝尔奖获得者Arber和博士生Dussoix表明λDNA被不同细菌宿主感染后会被排斥并降解,除非它对DNA进行了宿主特异性修饰,从而为限制性和修饰现象奠定了基础。 (R M)。大肠杆菌K-12的限制酶EcoKI于1968年纯化,需要S-腺苷甲硫氨酸(AdoMet)和ATP作为辅助因子。到本世纪末,有大量证据表明染色体基因座hsdK具有三个编码限制(R),修饰(M)和特异性(S)亚基的基因,它们组装成一个大于400 kDa的大复合体。 1970年代带来的信息是,EcoKI脱离了其DNA识别目标,该酶在将DNA转移到自身之外时仍被结合,并伴随着ATP水解和随后的双链缺口。这种易位事件在电子显微镜中产生了清晰可见的DNA环。 EcoKI成为具有原型DNA I型R-M酶,具有奇异的DNA易位特性,使人联想到解旋酶,可识别两部分不对称位点AAC(N6)GTGC。 1976年,hsdK基因座的克隆促进了对该复杂R-M复合物的分子理解,在优雅的“ pas de deux”中,Murray和Dryden基于大量实验数据和生物信息学构建了本模型。这篇综述庆祝了EcoKI的五十周年纪念日,并在DNA损伤后缓解限制性这一至关重要的问题上取得了令人兴奋的进展,该问题也于1953年首次报道,涉及细菌蛋白酶体ClpXP对R亚基活性的复杂控制,这一重要结果将继续科学家在EcoKI上走了50年之久。

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