UM  > Faculty of Health Sciences
Residential Collegefalse
Status已發表Published
The PTM profiling of CTCF reveals the regulation of 3D chromatin structure by O-GlcNAcylation
Tang, Xiuxiao1,2,3,4,5; Zeng, Pengguihang1,2,3,4; Liu, Kezhi1,2,3,4; Qing, Li1,2,3,4; Sun, Yifei1,2,3,4; Liu, Xinyi1,2,3,4; Lu, Lizi1,2,3,4; Wei, Chao1,2,3,4; Wang, Jia6; Jiang, Shaoshuai1,2,3,4; Sun, Jun7,8; Chang, Wakam9; Yu, Haopeng7,8; Chen, Hebing10; Zhou, Jiaguo5; Xu, Chengfang11; Fan, Lili12; Miao, Yi Liang13; Ding, Junjun1,2,3,4,7
2024-04-01
Source PublicationNature Communications
ISSN2041-1723
Volume15Issue:1Pages:2813
Abstract

CCCTC-binding factor (CTCF), a ubiquitously expressed and highly conserved protein, is known to play a critical role in chromatin structure. Post-translational modifications (PTMs) diversify the functions of protein to regulate numerous cellular processes. However, the effects of PTMs on the genome-wide binding of CTCF and the organization of three-dimensional (3D) chromatin structure have not been fully understood. In this study, we uncovered the PTM profiling of CTCF and demonstrated that CTCF can be O-GlcNAcylated and arginine methylated. Functionally, we demonstrated that O-GlcNAcylation inhibits CTCF binding to chromatin. Meanwhile, deficiency of CTCF O-GlcNAcylation results in the disruption of loop domains and the alteration of chromatin loops associated with cellular development. Furthermore, the deficiency of CTCF O-GlcNAcylation increases the expression of developmental genes and negatively regulates maintenance and establishment of stem cell pluripotency. In conclusion, these results provide key insights into the role of PTMs for the 3D chromatin structure.

KeywordCcctc-binding-factor Differential Expression Phosphorylation Sites Nuclear Factor Genome Gene Pluripotency Domains Dna Identification
DOI10.1038/s41467-024-47048-3
URLView the original
Indexed BySCIE
Language英語English
WOS Research AreaScience & Technology - Other Topics
WOS SubjectMultidisciplinary Sciences
WOS IDWOS:001195790900010
PublisherNATURE PORTFOLIO, HEIDELBERGER PLATZ 3, BERLIN 14197, GERMANY
Scopus ID2-s2.0-85189093583
Fulltext Access
Citation statistics
Document TypeJournal article
CollectionFaculty of Health Sciences
DEPARTMENT OF BIOMEDICAL SCIENCES
Corresponding AuthorChang, Wakam; Xu, Chengfang; Fan, Lili; Miao, Yi Liang; Ding, Junjun
Affiliation1.RNA Biomedical Institute, Sun Yat-Sen Memorial Hospital, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510080, China
2.Department of Rehabilitation Medicine, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong, 518107, China
3.Advanced Medical Technology Center, The First Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, Guangdong, China
4.Center for Stem Cell Biology and Tissue Engineering, Key Laboratory for Stem Cells and Tissue Engineering, Ministry of Education, Sun Yat-Sen University, Guangzhou, 510080, China
5.Department of Pharmacology and Cardiac & amp; Cerebral Vascular Research Center, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510080, China
6.GMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, 511436, China
7.West China Biomedical Big Data Center, West China Hospital/West China School of Medicine, Sichuan University, Chengdu, 610041, China
8.Med-X Center for Informatics, Sichuan University, Chengdu, 610041, China
9.Department of Biomedical Sciences, Faculty of Health Sciences, University of Macau, Taipa, Macao
10.Institute of Health Service and Transfusion Medicine, Beijing, 100850, China
11.The obstetric and gynecology Department of The third affiliated hospital of Sun Yat-Sen University, Guangzhou, China
12.Guangzhou Key Laboratory of Formula-Pattern of Traditional Chinese Medicine, School of Traditional Chinese Medicine, Jinan University, Guangzhou, Guangdong, China
13.Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei, China
Corresponding Author AffilicationFaculty of Health Sciences
Recommended Citation
GB/T 7714
Tang, Xiuxiao,Zeng, Pengguihang,Liu, Kezhi,et al. The PTM profiling of CTCF reveals the regulation of 3D chromatin structure by O-GlcNAcylation[J]. Nature Communications, 2024, 15(1), 2813.
APA Tang, Xiuxiao., Zeng, Pengguihang., Liu, Kezhi., Qing, Li., Sun, Yifei., Liu, Xinyi., Lu, Lizi., Wei, Chao., Wang, Jia., Jiang, Shaoshuai., Sun, Jun., Chang, Wakam., Yu, Haopeng., Chen, Hebing., Zhou, Jiaguo., Xu, Chengfang., Fan, Lili., Miao, Yi Liang., & Ding, Junjun (2024). The PTM profiling of CTCF reveals the regulation of 3D chromatin structure by O-GlcNAcylation. Nature Communications, 15(1), 2813.
MLA Tang, Xiuxiao,et al."The PTM profiling of CTCF reveals the regulation of 3D chromatin structure by O-GlcNAcylation".Nature Communications 15.1(2024):2813.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Tang, Xiuxiao]'s Articles
[Zeng, Pengguihang]'s Articles
[Liu, Kezhi]'s Articles
Baidu academic
Similar articles in Baidu academic
[Tang, Xiuxiao]'s Articles
[Zeng, Pengguihang]'s Articles
[Liu, Kezhi]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Tang, Xiuxiao]'s Articles
[Zeng, Pengguihang]'s Articles
[Liu, Kezhi]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.