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Resolving sequencing-based HIV-1 epitranscriptomics

delete2025-05-16
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M
Michael S. Bosmeny
J
João I. Mamede
K
Keith T. Gagnon *
DOI:10.1080/17501911.2025.2504333delete
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摘要

摘要

En 中文
HIV-1 RNA化学修饰的收集及其在病毒基因表达、宿主相互作用和病毒生命周期中的功能后果,被称为HIV-1表观转录组学,目前仍未被完全理解。尽管该领域正在发展,但多样的修饰发现方法、细胞系、HIV-1序列和生物信息学方法使得对HIV-1表观转录组的共识观点难以确立。本文综述了在HIV-1中识别和解释N6-甲基腺苷(m6A)、5-甲基胞嘧啶(m5C)、假尿苷(Psi)、2′-O-甲基化(Nm)和N4-乙酰胞嘧啶(ac4C)修饰的方法,包括抗体介导的选择方法、化学处理介导的选择方法以及通过纳米孔直接RNA测序进行检测。我们建议采用后者作为标准化的测序策略,以促进不同研究间的更好比较,并有助于阐明HIV-1表观转录组学。
Keyword:
HIV-1
epitranscriptomics
nanopore
sequencing
RNA modification

期刊

Epigenomics 封面图
Epigenomics
IF:
2.6
论文数:
1.8K
被引数:
3.4K

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