Lysine crotonylation in disease: mechanisms, biological functions and therapeutic targets

被引:0
|
作者
Ji, Yu [1 ,2 ,3 ]
Liu, Shanshan [1 ,2 ,3 ]
Zhang, Yiqiao [1 ,2 ,3 ]
Min, Yiyang [1 ,2 ,3 ]
Wei, Luyang [1 ,2 ,3 ]
Guan, Chengjian [1 ,2 ,3 ]
Yu, Huajing [1 ,2 ,3 ]
Zhang, Zhongtao [1 ,2 ,3 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Gen Surg, Beijing 100050, Peoples R China
[2] State Key Lab Digest Hlth, Dept Gen, Beijing 100050, Peoples R China
[3] Natl Clin Res Ctr Digest Dis, Beijing 100050, Peoples R China
基金
北京市自然科学基金;
关键词
LARGE-SCALE IDENTIFICATION; BROWN ADIPOSE-TISSUE; HISTONE CROTONYLATION; GENE-EXPRESSION; EPIGENETIC REGULATION; METABOLIC-REGULATION; COLORECTAL-CANCER; SORAFENIB; TRANSCRIPTION; ACETYLATION;
D O I
10.1186/s13072-025-00577-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lysine crotonylation (Kcr), a previously unknown post-translational modification (PTM), plays crucial roles in regulating cellular processes, including gene expression, chromatin remodeling, and cellular metabolism. Kcr is associated with various diseases, including neurodegenerative disorders, cancer, cardiovascular conditions, and metabolic syndromes. Despite advances in identifying crotonylation sites and their regulatory enzymes, the molecular mechanisms by which Kcr influences disease progression remain poorly understood. Understanding the interplay between Kcr and other acylation modifications may reveal opportunities for developing targeted therapies. This review synthesizes current research on Kcr, focusing on its regulatory mechanisms and disease associations, and highlights insights into future exploration in epigenetics and therapeutic interventions.
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页数:22
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