The State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 10085, P. R. China.
University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Adv Sci (Weinh). 2024 Sep;11(35):e2403376. doi: 10.1002/advs.202403376. Epub 2024 Jul 18.
Post-replicative DNA N-methyladenine (pr6mdA) can form via bona fide methylase-catalyzed adenine methylation, playing a pivotal role in embryonic development and other biological processes. Surprisingly, pre-methylated adenine can be erroneously incorporated into DNA as misincorporated N6-methyladenine (i6mdA) via DNA polymerase-mediated replication. Despite pr6mdA and i6mdA sharing identical chemical structures, their biological functions diverge significantly, presenting a substantial challenge in distinguishing between the two. Here, for the first-time, it is exploited that the adenosine deaminase-like (Adal) protein and a corresponding activity-null mutant to construct an Adal lentivirus toolkit. With this newly designed toolkit, both pr6mdA and i6mdA can be identified and quantified simultaneously. The presence of 6mdA in the bone marrow cells of mice is shown, with its levels serving as indicators for growth with age, probably reflecting the cellular stress-caused changes in RNA decay, nucleotide pool sanitation, and transcription. Collectively, a powerful toolkit to advance understanding of both pr6mdA and i6mdA is demonstrated.
复制后 DNA N-甲基腺嘌呤(pr6mdA)可以通过真正的甲基转移酶催化的腺嘌呤甲基化形成,在胚胎发育和其他生物过程中发挥关键作用。令人惊讶的是,预甲基化的腺嘌呤可以通过 DNA 聚合酶介导的复制错误地掺入 DNA 中,形成误掺入的 N6-甲基腺嘌呤(i6mdA)。尽管 pr6mdA 和 i6mdA 具有相同的化学结构,但它们的生物学功能却有很大的差异,这给区分两者带来了很大的挑战。在这里,首次利用腺苷脱氨酶样(Adal)蛋白及其相应的活性缺失突变体构建了一个 Adal 慢病毒工具包。利用这个新设计的工具包,可以同时鉴定和定量 pr6mdA 和 i6mdA。结果表明,在小鼠的骨髓细胞中存在 6mdA,其水平可以作为随年龄增长的生长指标,可能反映了 RNA 降解、核苷酸池净化和转录过程中细胞应激引起的变化。总之,该研究展示了一种强大的工具包,可以促进对 pr6mdA 和 i6mdA 的理解。