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  4. PARP-1 expression in the mouse is controlled by an autoregulatory loop: PARP-1 binding to an upstream S/MAR element and to a novel recognition motif in its promoter suppresses transcription.
 
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Titre

PARP-1 expression in the mouse is controlled by an autoregulatory loop: PARP-1 binding to an upstream S/MAR element and to a novel recognition motif in its promoter suppresses transcription.

Type
article
Institution
Externe
Périodique
Journal of Molecular Biology  
Auteur(s)
Vidaković, M.
Auteure/Auteur
Gluch, A.
Auteure/Auteur
Qiao, J.
Auteure/Auteur
Oumard, A.
Auteure/Auteur
Frisch, M.
Auteure/Auteur
Poznanović, G.
Auteure/Auteur
Bode, J.
Auteure/Auteur
Liens vers les personnes
Qiao, Junhua  
ISSN
1089-8638[electronic], 0022-2836[linking]
Statut éditorial
Publié
Date de publication
2009
Volume
388
Numéro
4
Première page
730
Dernière page/numéro d’article
750
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
This work identifies central components of a feedback mechanism for the expression of mouse poly(ADP-ribose) polymerase-1 (PARP-1). Using the stress-induced duplex destabilization algorithm, multiple base-unpairing regions (BURs) could be localized in the 5' region of the mouse PARP-1 gene (muPARP-1). Some of these could be identified as scaffold/matrix-attachment regions (S/MARs), suggesting an S/MAR-mediated transcriptional regulation. PARP-1 binding to the most proximal element, S/MAR 1, and to three consensus motifs, AGGCC, in its own promoter (basepairs -956 to +100), could be traced by electrophoretic mobility-shift assay. The AGGCC-complementary GGCCT motif was detected by cis-diammine-dichloro platinum cross-linking and functionally characterized by the effects of site-directed mutagenesis on its performance in wild type (PARP-1(+/+)) and PARP-1 knockout cells (PARP-1(-/-)). Mutation of the central AGGCC tract at basepairs -554 to -550 prevented PARP-1/promoter interactions, whereby muPARP-1 expression became up-regulated. Transfection of a series of reporter gene constructs with or without S/MAR 1 (basepairs -1523 to -1007) and the more distant S/MAR 2 (basepairs -8373 to -6880), into PARP-1(+/+) as well as PARP-1(-/-) cells, revealed an additional, major level of muPARP-1 promoter down-regulation, triggered by PARP-1 binding to S/MAR 1. We conclude that S/MAR 1 represents an upstream control element that acts in conjunction with the muPARP-1 promoter. These interactions are part of a negative autoregulatory loop.
Sujets

Animals

Base Sequence

Binding Sites

Cells, Cultured

Cross-Linking Reagent...

DNA/chemistry

DNA/genetics

DNA Damage

Fibroblasts/cytology

Fibroblasts/physiolog...

Formaldehyde/chemistr...

Gene Expression Regul...

Genes, Reporter

Humans

Mice

Mice, Knockout

Molecular Sequence Da...

Poly(ADP-ribose) Poly...

Poly(ADP-ribose) Poly...

Promoter Regions, Gen...

Protein Binding

Regulatory Sequences,...

Transcription, Geneti...

PID Serval
serval:BIB_0A8159EF268B
DOI
10.1016/j.jmb.2009.03.032
PMID
19303024
Permalien
https://iris.unil.ch/handle/iris/80737
Date de création
2010-06-16T10:13:15.098Z
Date de création dans IRIS
2025-05-20T17:05:29Z
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