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病毒DNA包装:噬菌体λ所采用的策略。

Virus DNA packaging: the strategy used by phage lambda.

作者信息

Catalano C E, Cue D, Feiss M

机构信息

School of Pharmacy, University of Colorado Health Science Center, Denver 80262, USA.

出版信息

Mol Microbiol. 1995 Jun;16(6):1075-86. doi: 10.1111/j.1365-2958.1995.tb02333.x.

Abstract

Phage lambda, like a number of other large DNA bacteriophages and the herpesviruses, produces concatemeric DNA during DNA replication. The concatemeric DNA is processed to produce unit-length, virion DNA by cutting at specific sites along the concatemer. DNA cutting is co-ordinated with DNA packaging, the process of translocation of the cut DNA into the preformed capsid precursor, the prohead. A key player in the lambda DNA packaging process is the phage-encoded enzyme terminase, which is involved in (i) recognition of the concatemeric lambda DNA; (ii) initiation of packaging, which includes the introduction of staggered nicks at cosN to generate the cohesive ends of virion DNA and the binding of the prohead; (iii) DNA packaging, possibly including the ATP-driven DNA translocation; and (iv) following translocation, the cutting of the terminal cosN to complete DNA packaging. To one side of cosN is the site cosB, which plays a role in the initiation of packaging; along with ATP, cosB stimulates the efficiency and adds fidelity to the endonuclease activity of terminase in cutting cosN. cosB is essential for the formation of a post-cleavage complex with terminase, complex I, that binds the prohead, forming a ternary assembly, complex II. Terminase interacts with cosN through its large subunit, gpA, and the small terminase subunit, gpNu1, interacts with cosB. Packaging follows complex II formation. cosN is flanked on the other side by the site cosQ, which is needed for termination, but not initiation, of DNA packaging. cosQ is required for cutting of the second cosN, i.e. the cosN at which termination occurs. DNA packaging in lambda has aspects that differ from other lambda DNA transactions. Unlike the site-specific recombination system of lambda, for DNA packaging the initial site-specific protein assemblage gives way to a mobile, translocating complex, and unlike the DNA replication system of lambda, the same protein machinery is used for both initiation and translocation during lambda DNA packaging.

摘要

λ噬菌体与许多其他大型DNA噬菌体及疱疹病毒一样,在DNA复制过程中产生串联体DNA。串联体DNA通过沿串联体的特定位点切割来加工,以产生单位长度的病毒体DNA。DNA切割与DNA包装相协调,DNA包装是将切割后的DNA转运到预先形成的衣壳前体即原头部的过程。λ噬菌体DNA包装过程中的一个关键参与者是噬菌体编码的酶末端酶,它参与:(i)串联体λ噬菌体DNA的识别;(ii)包装的起始,包括在cosN处引入交错切口以产生病毒体DNA的粘性末端以及原头部的结合;(iii)DNA包装,可能包括ATP驱动的DNA转运;以及(iv)转运后,切割末端的cosN以完成DNA包装。在cosN的一侧是cosB位点,它在包装起始中起作用;与ATP一起,cosB刺激效率并增加末端酶切割cosN时的内切核酸酶活性的保真度。cosB对于与末端酶形成切割后复合物(复合物I)至关重要,该复合物结合原头部,形成三元组装体(复合物II)。末端酶通过其大亚基gpA与cosN相互作用,而小末端酶亚基gpNu1与cosB相互作用。包装在复合物II形成后进行。cosN的另一侧是cosQ位点,它是DNA包装终止而非起始所必需的。cosQ是切割第二个cosN即发生终止的cosN所必需的。λ噬菌体中的DNA包装具有与其他λ噬菌体DNA交易不同的方面。与λ噬菌体的位点特异性重组系统不同,对于DNA包装,最初的位点特异性蛋白质组装让位于一个移动的、正在转运的复合物,并且与λ噬菌体的DNA复制系统不同,在λ噬菌体DNA包装过程中,相同蛋白质机制用于起始和转运。

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