Histone Modification Pathways Suppressing Cryptic Transcription.

IF 2.5 Q3 GENETICS & HEREDITY Epigenomes Pub Date : 2024-11-12 DOI:10.3390/epigenomes8040042
Hong-Yeoul Ryu
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Abstract

Cryptic transcription refers to the unintended expression of non-canonical sites within the genome, producing aberrant RNA and proteins that may disrupt cellular functions. In this opinion piece, I will explore the role of histone modifications in modulating cryptic transcription and its implications for gene expression and cellular integrity, particularly with a focus on H3K36 and H3K4 methylation marks. H3K36 tri-methylation plays a crucial role in maintaining chromatin integrity by facilitating the recruitment of the Rpd3S histone deacetylase (HDAC) complex, which helps restore closed chromatin states following transcription and prevents cryptic initiation within gene bodies. In parallel, crosstalk between H3K4 di-methylation and histone ubiquitylation and sumoylation is critical for recruiting the Set3 HDAC complex, which maintains low histone acetylation levels in gene bodies and further suppresses cryptic transcription. Therefore, by elucidating these regulatory mechanisms, this opinion highlights the intricate interplay of histone modifications in preserving transcriptional fidelity and suggests potential pathways for future research to develop novel therapies for age-related disorders and other diseases associated with dysregulated gene expression.

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抑制隐性转录的组蛋白修饰途径
隐性转录是指基因组内非规范位点的意外表达,产生的异常 RNA 和蛋白质可能会破坏细胞功能。在这篇观点文章中,我将探讨组蛋白修饰在调节隐性转录中的作用及其对基因表达和细胞完整性的影响,尤其是重点关注 H3K36 和 H3K4 甲基化标记。H3K36 三甲基化在维持染色质完整性方面起着至关重要的作用,它能促进 Rpd3S 组蛋白去乙酰化酶(HDAC)复合物的招募,从而帮助恢复转录后的封闭染色质状态,防止基因体内的隐性启动。与此同时,H3K4 二甲基化与组蛋白泛素化和苏木酰化之间的相互影响对于招募 Set3 HDAC 复合物至关重要,Set3 HDAC 复合物可维持基因体内较低的组蛋白乙酰化水平,进一步抑制隐性转录。因此,通过阐明这些调控机制,本研究报告强调了组蛋白修饰在保持转录保真度方面错综复杂的相互作用,并为未来的研究提出了潜在的途径,以开发治疗老年相关疾病和其他与基因表达失调有关的疾病的新疗法。
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来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
期刊最新文献
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