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组蛋白修饰作为个体特异性表观遗传调节因子:法医遗传学和死后分析的机遇

Histone Modifications as Individual-Specific Epigenetic Regulators: Opportunities for Forensic Genetics and Postmortem Analysis.

作者信息

Yang Sheng, Chen Liqin, Lin Miaofang, Shen Chengwan, Reheman Aikebaier

机构信息

Fujian Key Laboratory of Toxicant and Drug Toxicology, Medical College, Ningde Normal University, Ningde 352100, China.

Fujian Zhengyang Forensic Appraisal Institute, Ningde 352100, China.

出版信息

Genes (Basel). 2025 Aug 7;16(8):940. doi: 10.3390/genes16080940.

Abstract

Histone post-translational modifications (PTMs) have emerged as promising epigenetic biomarkers with increasing forensic relevance. Unlike conventional genetic markers such as short tandem repeats (STRs), histone modifications can offer additional layers of biological information, capturing individual-specific regulatory states and remaining detectable even in degraded forensic samples. This review highlights recent advances in understanding histone PTMs in forensic contexts, focusing on three key domains: analysis of degraded biological evidence, differentiation of monozygotic (MZ) twins, and postmortem interval (PMI) estimation. We summarize experimental findings from human cadavers, animal models, and typical forensic samples including bone, blood, and muscle, illustrating the stability and diagnostic potential of marks such as H3K4me3, H3K27me3, and γ-H2AX. Emerging technologies including CUT&Tag, MALDI imaging, and nanopore-based sequencing offer novel opportunities to profile histone modifications at high resolution and low input. Despite technical challenges, these findings support the feasibility of histone-based biomarkers as complementary tools for forensic identification and temporal analysis. Future work should prioritize methodological standardization, inter-laboratory validation, and integration into forensic workflows. However, the forensic applicability of these modifications remains largely unvalidated, and further studies are required to assess their reliability in casework contexts.

摘要

组蛋白翻译后修饰(PTMs)已成为具有越来越高法医相关性的有前景的表观遗传生物标志物。与短串联重复序列(STRs)等传统遗传标记不同,组蛋白修饰可以提供额外层次的生物学信息,捕捉个体特异性调控状态,甚至在降解的法医样本中仍可检测到。本综述重点介绍了在法医背景下理解组蛋白PTMs的最新进展,聚焦于三个关键领域:降解生物证据的分析、同卵双胞胎(MZ)的区分以及死后间隔时间(PMI)的估计。我们总结了来自人类尸体、动物模型以及包括骨骼、血液和肌肉在内的典型法医样本的实验结果,阐述了诸如H3K4me3、H3K27me3和γ-H2AX等标记的稳定性和诊断潜力。包括CUT&Tag、基质辅助激光解吸电离成像(MALDI成像)和基于纳米孔的测序在内的新兴技术为高分辨率、低输入量分析组蛋白修饰提供了新机遇。尽管存在技术挑战,但这些发现支持了基于组蛋白的生物标志物作为法医鉴定和时间分析补充工具的可行性。未来的工作应优先进行方法标准化、实验室间验证以及整合到法医工作流程中。然而,这些修饰在法医方面的适用性在很大程度上仍未得到验证,需要进一步研究以评估它们在实际案件中的可靠性。

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