p53 and its two homologues, p73 and p63, share considerable structural similarities, an ability to interact between themselves and to transactivate the same promoters, including for example p21. Furthermore, p73 can induce cell death via its interaction with c-Abl, In contrast, p63 has been demonstrated to be essential for limb and skin formation. We evaluated the expression of p63 and p73 in differentiating human keratinocytes in vitro. Skin biopsy and primary cultures of normal human epidermal keratinocytes (NHEK) express both p73 and p63. NHEK induced to differentiate in vitro by high calcium exposure show induction of p73 delta and downregulation of all isoforms of p63. This latter gene is predominantly expressed in its transcriptionally inactive form, Delta Np63. We further evaluated the effect of either p73s or p63 transfected in either NHEK or transformed human keratinocytes (HaCat cells). p73 gamma, delta, and p63 were able to transactivate the promoters of loricrin and involucrin in both NHEK and HaCat cells. These results suggest the involvement of both p73 and p63 genes in keratinocyte terminal differentiation. (C) 2000 Academic Press.

De Laurenzi, V., Rossi, A., Terrinoni, A., Barcaroli, D., Levrero, M., Costanzo, A., et al. (2000). p63 and p73 transactivate differentiation gene promoters in human keratinocytes. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 273(1), 342-346 [10.1006/bbrc.2000.2932].

p63 and p73 transactivate differentiation gene promoters in human keratinocytes

De Laurenzi V.;Rossi A.;Terrinoni A.;Barcaroli D.;Costanzo A.;Guerrieri P.;Melino G.
2000-01-01

Abstract

p53 and its two homologues, p73 and p63, share considerable structural similarities, an ability to interact between themselves and to transactivate the same promoters, including for example p21. Furthermore, p73 can induce cell death via its interaction with c-Abl, In contrast, p63 has been demonstrated to be essential for limb and skin formation. We evaluated the expression of p63 and p73 in differentiating human keratinocytes in vitro. Skin biopsy and primary cultures of normal human epidermal keratinocytes (NHEK) express both p73 and p63. NHEK induced to differentiate in vitro by high calcium exposure show induction of p73 delta and downregulation of all isoforms of p63. This latter gene is predominantly expressed in its transcriptionally inactive form, Delta Np63. We further evaluated the effect of either p73s or p63 transfected in either NHEK or transformed human keratinocytes (HaCat cells). p73 gamma, delta, and p63 were able to transactivate the promoters of loricrin and involucrin in both NHEK and HaCat cells. These results suggest the involvement of both p73 and p63 genes in keratinocyte terminal differentiation. (C) 2000 Academic Press.
2000
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/12 - BIOCHIMICA CLINICA E BIOLOGIA MOLECOLARE CLINICA
Settore BIO/11 - BIOLOGIA MOLECOLARE
English
Con Impact Factor ISI
p73; p63; p53; apoptosis; differentiation; keratinocytes; skin; Calcium; Cell Differentiation; Cell Line, Transformed; Cells, Cultured; DNA-Binding Proteins; Down-Regulation; Genes, Reporter; Genes, Tumor Suppressor; Humans; Keratinocytes; Membrane Proteins; Nuclear Proteins; Phosphoproteins; Promoter Regions, Genetic; Protein Isoforms; Protein Precursors; RNA, Messenger; Transcription Factors; Transcriptional Activation; Transfection; Tumor Protein p73; Tumor Suppressor Proteins; Trans-Activators
De Laurenzi, V., Rossi, A., Terrinoni, A., Barcaroli, D., Levrero, M., Costanzo, A., et al. (2000). p63 and p73 transactivate differentiation gene promoters in human keratinocytes. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 273(1), 342-346 [10.1006/bbrc.2000.2932].
De Laurenzi, V; Rossi, A; Terrinoni, A; Barcaroli, D; Levrero, M; Costanzo, A; Knight, Ra; Guerrieri, P; Melino, G
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/240835
Citazioni
  • ???jsp.display-item.citation.pmc??? 31
  • Scopus 122
  • ???jsp.display-item.citation.isi??? 120
social impact