Sumoylation dynamics during keratinocyte differentiation

被引:58
作者
Deyrieux, Adeline F.
Rosas-Acosta, German
Ozbun, Michelle A.
Wilson, Van G. [1 ]
机构
[1] Texas A&M Univ, Hlth Sci Ctr, Dept Mol & Microbial Pathogenesis, Coll Med, College Stn, TX 77843 USA
[2] Univ New Mexico, Sch Med, Dept Mol Genet & Microbiol, CFR 303, Albuquerque, NM 87131 USA
关键词
keratinocyte; differentiation; SUMO; HaCaT; Ubc9;
D O I
10.1242/jcs.03317
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
SUMO modification regulates the activity of numerous transcription factors that have a direct role in cell-cycle progression, apoptosis, cellular proliferation, and development, but its role in differentiation processes is less clear. Keratinocyte differentiation requires the coordinated activation of a series of transcription factors, and as several crucial keratinocyte transcription factors are known to be SUMO substrates, we investigated the role of sumoylation in keratinocyte differentiation. In a human keratinocyte cell line model (HaCaT cells), Ca2+-induced differentiation led to the transient and coordinated transcriptional activation of the genes encoding crucial sumoylation system components, including SAE1, SAE2, Ubc9, SENP1, Miz-1 (PIASx beta), SUMO2 and SUMO3. The increased gene expression resulted in higher levels of the respective proteins and changes in the pattern of sumoylated substrate proteins during the differentiation process. Similarly to the HaCaT results, stratified human foreskin keratinocytes showed an upregulation of Ubc9 in the suprabasal layers. Abrogation of sumoylation by Gam1 expression severely disrupted normal HaCaT differentiation, consistent with an important role for sumoylation in the proper progression of this biological process.
引用
收藏
页码:125 / 136
页数:12
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