Perp is a p63-regulated gene essential for epithelial integrity

被引:262
作者
Ihrie, RA
Marques, MR
Nguyen, BT
Horner, JS
Papazoglu, C
Bronson, RT
Mills, AA
Attardi, LD [1 ]
机构
[1] Stanford Univ, Sch Med, Div Radiat & Canc Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Radiat Oncol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[4] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[5] SUNY Stony Brook, Grad Program Genet, Stony Brook, NY 11794 USA
[6] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.cell.2005.01.008
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
p63 is a master regulator of stratified epithelial development that is both necessary and sufficient for specitying this multifaceted program. We show here that Perp, a tetraspan membrane protein originally identified as an apoptosis-associated target of the p53 tumor suppressor, is the first direct target of p63 clearly involved in mediating this developmental program in vivo. During embryogenesis, Perp is expressed in an epithelial pattern, and its expression depends on p63. Perp(-/-) mice die postnatally, with dramatic blistering in stratified epithelia symptomatic of compromised adhesion. Perp localizes specifically to desmosomes, adhesion junctions important for tissue integrity, and numerous structural defects in desmosomes are observed in Perp-deficient skin, suggesting a role for Perp in promoting the stable assembly of desmosomal adhesive complexes. These findings demonstrate that Perp is a key effector in the p63 developmental program, playing an essential role in an adhesion subprogram central to epithelial integrity and homeostasis.
引用
收藏
页码:843 / 856
页数:14
相关论文
共 31 条
[1]  
Attardi LD, 2000, GENE DEV, V14, P704
[2]   The role of p53 in tumour suppression: lessons from mouse models [J].
Attardi, LD ;
Jacks, T .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (01) :48-63
[3]  
Bornslaeger EA, 2001, J CELL SCI, V114, P727
[4]   Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms [J].
Chen, L ;
Chetkovich, DM ;
Petralia, RS ;
Sweeney, NT ;
Kawasaki, Y ;
Wenthold, RJ ;
Bredt, DS ;
Nicoll, RA .
NATURE, 2000, 408 (6815) :936-943
[5]   Coupling assembly of the E-cadherin/β-catenin complex to efficient endoplasmic reticulum exit and basal-lateral membrane targeting of E-cadherin in polarized MDCK cells [J].
Chen, YT ;
Stewart, DB ;
Nelson, WJ .
JOURNAL OF CELL BIOLOGY, 1999, 144 (04) :687-699
[6]   p63α and ΔNp63α can induce cell cycle arrest and apoptosis and differentially regulate p53 target genes [J].
Dohn, M ;
Zhang, SZ ;
Chen, XB .
ONCOGENE, 2001, 20 (25) :3193-3205
[7]   REDD1, a developmentally regulated transcriptional target of p63 and p53, links p63 to regulation of reactive oxygen species [J].
Ellisen, LW ;
Ramsayer, KD ;
Johannessen, CM ;
Yang, A ;
Beppu, H ;
Minda, K ;
Oliner, JD ;
McKeon, F ;
Haber, DA .
MOLECULAR CELL, 2002, 10 (05) :995-1005
[8]   p63 and p73 are required for p53-dependent apoptosis in response to DNA damage [J].
Flores, ER ;
Tsai, KY ;
Crowley, D ;
Sengupta, S ;
Yang, A ;
McKeon, F ;
Jacks, T .
NATURE, 2002, 416 (6880) :560-564
[9]  
FRANTZ GD, 1994, J NEUROSCI, V14, P5725
[10]   Getting under the skin of epidermal morphogenesis [J].
Fuchs, E ;
Raghavan, S .
NATURE REVIEWS GENETICS, 2002, 3 (03) :199-209