Locus of (IL-9) control: IL9 epigenetic regulation in cellular function and human disease

被引:1
|
作者
Son, Aran [1 ]
Baral, Ishita [2 ]
Falduto, Guido H. [2 ]
Schwartz, Daniella M. [2 ]
机构
[1] Int Sch Adv Studies SISSA, Neurosci Dept, Via Bonomea 265, I-34136 Trieste, Italy
[2] Univ Pittsburgh, Div Rheumatol & Clin Immunol, Pittsburgh, PA 15260 USA
来源
EXPERIMENTAL AND MOLECULAR MEDICINE | 2024年 / 56卷 / 06期
关键词
TRANSCRIPTION FACTOR PU.1; T-HELPER; 9; GENE POLYMORPHISMS; SUPER-ENHANCERS; T(H)9 CELLS; TH9; CELLS; KAPPA-B; INTERLEUKIN-9; EXPRESSION; DIFFERENTIATION;
D O I
10.1038/s12276-024-01241-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-9 (IL-9) is a multifunctional cytokine with roles in a broad cross-section of human diseases. Like many cytokines, IL-9 is transcriptionally regulated by a group of noncoding regulatory elements (REs) surrounding the IL9 gene. These REs modulate IL-9 transcription by forming 3D loops that recruit transcriptional machinery. IL-9-promoting transcription factors (TFs) can bind REs to increase locus accessibility and permit chromatin looping, or they can be recruited to already accessible chromatin to promote transcription. Ample mechanistic and genome-wide association studies implicate this interplay between IL-9-modulating TFs and IL9 cis-REs in human physiology, homeostasis, and disease.
引用
收藏
页码:1331 / 1339
页数:9
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