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嵌入DNA中的核糖核苷引发的非靶向突变

Untargeted Mutation Triggered by Ribonucleoside Embedded in DNA.

作者信息

Suzuki Tetsuya, Yasui Kiyoharu, Komatsu Yasuo, Kamiya Hiroyuki

机构信息

Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan.

Department of Life Science and Biotechnology, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba, Ibaraki 305-8560, Japan.

出版信息

Int J Mol Sci. 2024 Dec 22;25(24):13708. doi: 10.3390/ijms252413708.

DOI:10.3390/ijms252413708
PMID:39769470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11679520/
Abstract

DNA polymerases frequently misincorporate ribonucleoside 5'-triphosphates into nascent DNA strands. This study examined the effects of an incorporated ribonucleoside on untargeted mutations in human cells. Riboguanosine (rG) was introduced into the downstream region of the gene to preferentially detect the untargeted mutations. The plasmid containing rG was transfected into U2OS cells and the replicated DNA was recovered after 48 h. The mutation analysis using the indicator RF01 strain showed the frequent induction of untargeted base substitutions at the G bases of 5'-GpA-3' dinucleotides, similar to action-at-a-distance mutations induced by an oxidatively damaged base, 8-oxo-7,8-dihydroguanine, and an apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like 3 (APOBEC3) cytosine deaminase. APOBEC3B was then knocked down by RNA interference and the plasmid bearing rG was introduced into the knockdown cells. The untargeted mutations at 5'-pA-3' sites were reduced by ~80%. These results suggested that ribonucleosides embedded in DNA induce base substitution mutations at G bases in the same strand by an APOBEC3B-dependent mechanism, implying that ribonucleosides contribute to APOBEC3-dependent cancer initiation events.

摘要

DNA聚合酶经常将核糖核苷5'-三磷酸错误掺入新生DNA链中。本研究检测了掺入的核糖核苷对人类细胞中非靶向突变的影响。将核糖鸟苷(rG)引入基因的下游区域,以优先检测非靶向突变。将含有rG的质粒转染到U2OS细胞中,48小时后回收复制的DNA。使用指示菌株RF01进行的突变分析显示,在5'-GpA-3'二核苷酸的G碱基处频繁诱导非靶向碱基替换,类似于由氧化损伤碱基8-氧代-7,8-二氢鸟嘌呤和载脂蛋白B mRNA编辑酶催化多肽样3(APOBEC3)胞嘧啶脱氨酶诱导的远距离作用突变。然后通过RNA干扰敲低APOBEC3B,并将携带rG的质粒引入敲低细胞中。5'-pA-3'位点的非靶向突变减少了约80%。这些结果表明,嵌入DNA中的核糖核苷通过APOBEC3B依赖性机制在同一条链的G碱基处诱导碱基替换突变,这意味着核糖核苷有助于APOBEC3依赖性癌症起始事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/dbe066924f69/ijms-25-13708-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/120efd3a6150/ijms-25-13708-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/0ce7b3a850b4/ijms-25-13708-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/4096cb21597c/ijms-25-13708-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/b228e22307fe/ijms-25-13708-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/6a29a7492557/ijms-25-13708-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/dbe066924f69/ijms-25-13708-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/120efd3a6150/ijms-25-13708-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/0ce7b3a850b4/ijms-25-13708-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/4096cb21597c/ijms-25-13708-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/b228e22307fe/ijms-25-13708-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/6a29a7492557/ijms-25-13708-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ea/11679520/dbe066924f69/ijms-25-13708-g006.jpg

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本文引用的文献

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Biol Pharm Bull. 2024;47(7):1275-1281. doi: 10.1248/bpb.b24-00258.
2
Action-at-a-distance mutations induced by 8-oxo-7,8-dihydroguanine are dependent on APOBEC3.由8-氧代-7,8-二氢鸟嘌呤诱导的远距离作用突变依赖于载脂蛋白B编辑酶催化多肽样蛋白3。
Mutagenesis. 2024 Feb 8;39(1):24-31. doi: 10.1093/mutage/gead023.
3
Easily-controllable, helper phage-free single-stranded phagemid production system.
易于控制的、无辅助噬菌体的单链噬菌粒生产系统。
Genes Environ. 2022 Nov 16;44(1):25. doi: 10.1186/s41021-022-00254-1.
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Biased distribution of action-at-a-distance mutations by 8-oxo-7,8-dihydroguanine.8-氧代-7,8-二氢鸟嘌呤导致的远距离作用突变的偏倚分布。
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Mechanisms of APOBEC3 mutagenesis in human cancer cells.APOBEC3 在人类癌细胞中致突变的机制。
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Functions and consequences of AID/APOBEC-mediated DNA and RNA deamination.AID/APOBEC 介导的 DNA 和 RNA 脱氨酶的功能和后果。
Nat Rev Genet. 2022 Aug;23(8):505-518. doi: 10.1038/s41576-022-00459-8. Epub 2022 Mar 7.
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FEBS J. 2022 Feb;289(3):808-831. doi: 10.1111/febs.16202. Epub 2021 Oct 4.
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