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
相关论文
共 87 条
[21]   THE ROLE OF KERATIN SUBFAMILIES AND KERATIN PAIRS IN THE FORMATION OF HUMAN EPIDERMAL INTERMEDIATE FILAMENTS [J].
EICHNER, R ;
SUN, TT ;
AEBI, U .
JOURNAL OF CELL BIOLOGY, 1986, 102 (05) :1767-1777
[22]   Transcription factor AP-2 interacts with the SUMO-conjugating enzyme UBC9 and is sumolated in vivo [J].
Eloranta, JJ ;
Hurst, HC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (34) :30798-30804
[23]   Mechanisms of calcium signaling and function in lymphocytes [J].
Freedman, BD .
CRITICAL REVIEWS IN IMMUNOLOGY, 2006, 26 (02) :97-111
[24]   CHANGES IN KERATIN GENE-EXPRESSION DURING TERMINAL DIFFERENTIATION OF THE KERATINOCYTE [J].
FUCHS, E ;
GREEN, H .
CELL, 1980, 19 (04) :1033-1042
[25]   EPIDERMAL DIFFERENTIATION - THE BARE ESSENTIALS [J].
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :2807-2814
[26]   The protein stability and transcriptional activity of p63α are regulated by SUMO-1 conjugation [J].
Ghioni, P ;
D'Alessandra, Y ;
Mansueto, G ;
Jaffray, E ;
Hay, RT ;
La Mantia, G ;
Guerrini, L .
CELL CYCLE, 2005, 4 (01) :183-190
[27]   Post-translational modification by the small ubiquitin-related modifier SUMO has big effects on transcription factor activity [J].
Gill, G .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (02) :108-113
[28]   SUMO and transcriptional regulation [J].
Girdwood, DWH ;
Tatham, MH ;
Hay, RT .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2004, 15 (02) :201-210
[29]   Characterization of a family of nucleolar SUMO-specific proteases with preference for SUMO-2 or SUMO-3 [J].
Gong, Limin ;
Yeh, Edward T. H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (23) :15869-15877
[30]   Proteomic analysis of SUM04 substrates in HEK293 cells under serum starvation-induced stress [J].
Guo, DH ;
Han, JY ;
Adam, BL ;
Colburn, NH ;
Wang, MH ;
Dong, Z ;
Eizirik, DL ;
She, JX ;
Wang, CY .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 337 (04) :1308-1318