Transcriptional Repression of miR-34 Family Contributes to p63-Mediated Cell Cycle Progression in Epidermal Cells

被引:113
作者
Antonini, Dario [1 ]
Russo, Monia T. [1 ]
De Rosa, Laura [1 ,2 ]
Gorrese, Marisa [1 ]
Del Vecchio, Luigi [1 ,3 ]
Missero, Caterina [1 ,2 ]
机构
[1] CEINGE Biotecnol Avanzate, I-80145 Naples, Italy
[2] IRCCS Fdn SDN, Naples, Italy
[3] Univ Naples Federico 2, Dipartimento Biochim & Biotecnol Med, Naples, Italy
关键词
GENE-EXPRESSION; CANCER-CELLS; P53; HOMOLOG; STEM-CELLS; P63; TARGET; ARREST; MORPHOGENESIS; APOPTOSIS; SKIN;
D O I
10.1038/jid.2009.438
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
p63, a p53 family member, is highly expressed in the basal proliferative compartment of the epidermis and its expression has been correlated with the growth ability and regenerative capacity of keratinocytes. In this study we report a mechanism through which p63 maintains cell cycle progression by directly repressing miR-34a and miR-34c. In the absence of p63, increased levels of miR-34a and miR-34c were observed in primary keratinocytes and in embryonic skin, with concomitant G1-phase arrest and inhibition of the cell cycle regulators cyclin D1 and cyclin-dependent kinase 4 (Cdk4). p63 directly bound to p53-consensus sites in both miR-34a and miR-34c regulatory regions and inhibited their activity. Concomitant downregulation of miR-34a and miR-34c substantially restored cell cycle progression and expression of cyclin D1 and Cdk4. Our data indicate that specific miR-34 family members have a significant role downstream of p63 in controlling epidermal cell proliferation.
引用
收藏
页码:1249 / 1257
页数:9
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