噬菌体Z基因组生物合成途径研究进展。

Q3 Medicine 遗传 Pub Date : 2023-10-20 DOI:10.16288/j.yczz.23-059
Hui-Yu Chen, Su-Wen Zhao
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引用次数: 0

摘要

噬菌体基因组中有大量的碱基修饰,主要是为了避免宿主核酸内切酶的消化。40多年前,研究人员发现,在蓝噬菌体S-2L的DNA中,2-氨基-腺嘌呤(Z)完全取代腺嘌呤(A),并与胸腺嘧啶(T)形成三个氢键的互补配对,形成了一个独特的“Z基因组”。近年来,研究人员在各种噬菌体中发现并验证了Z基因组的生物合成途径,构成了一个多酶系统。该系统包括噬菌体编码的酶脱氧2'-氨基腺苷酸琥珀酸合成酶(PurZ)、脱氧三磷酸腺苷水解酶(dATPase/DatZ)、去氧腺苷/脱氧鸟苷三磷酸焦磷酸酶(DUF550/MazZ)和DNA聚合酶(DpoZ)。在这篇综述中,我们简要概述了噬菌体中多种修饰核苷的历史发现,然后全面总结了Z基因组生物合成途径中多种酶的研究进展。最后,讨论了Z基因组及其酶在其生物合成途径中的潜在应用,为该领域的研究提供参考。
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Progress on Z genome biosynthetic pathway of bacteriophage.

There are abundant base modifications in bacteriophages' genomes, mainly for avoiding the digestion of host endonucleases. More than 40 years ago, researchers discovered that 2-amino-adenine (Z) completely replaced adenine (A) and forms a complementary pairing with three hydrogen bonds with thymine (T) in the DNA of cyanophage S-2L, forming a distinct "Z-genome". In recent years, researchers have discovered and validated the biosynthetic pathway of Z-genome in various bacteriophages, constituting a multi-enzyme system. This system includes the phage-encoded enzymes deoxy-2'-aminoadenylosuccinate synthetase (PurZ), deoxyadenosine triphosphate hydrolase (dATPase/DatZ), deoxyadenosine/deoxyguanosine triphosphate pyrophosphatase (DUF550/MazZ) and DNA polymerase (DpoZ). In this review, we provide a concise overview of the historical discovery on diversely modified nucleosides in bacteriophages, then we comprehensively summarize the research progress on multiple enzymes involved in the Z-genome biosynthetic pathway. Finally, the potential applications of the Z-genome and the enzymes in its biosynthetic pathway are discussed in order to provide reference for research in this field.

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来源期刊
遗传
遗传 Medicine-Medicine (all)
CiteScore
2.50
自引率
0.00%
发文量
6699
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