PARP-1 and gene regulation: progress and puzzles

Mol Aspects Med. 2013 Dec;34(6):1109-23. doi: 10.1016/j.mam.2013.01.005. Epub 2013 Jan 26.

Abstract

Poly(ADP-ribose) polymerase-1 (PARP-1), also referred to as ADP-ribosyltransferase Diphtheria toxin-like 1 (ARTD1), is an abundant nuclear protein that plays key roles in a variety of nuclear processes, including the regulation of transcription. PARP-1 possesses an intrinsic enzymatic activity that catalyzes the transfer of ADP-ribose (ADPR) units from nicotinamide adenine dinucleotide (NAD(+)) onto target gene regulatory proteins, thereby modulating their activities. Although great strides have been made in the past decade in deciphering the seemingly opposing and varied roles of PARP-1 in gene regulation, many puzzles remain. In this review, we discuss the current state of understanding in this area, especially how PARP-1 interfaces with various components of gene regulatory pathways (e.g., the basal transcription machinery, DNA-binding transcription factors, coregulators, chromatin remodeling, histone modifications, and DNA methylation). In addition, we discuss some gene-specific, cell type-specific, and cell state-specific effects of PARP-1 on gene regulation, which might contribute to its biological functions. Finally, we review some of the recent progress targeting PARPs using chemical inhibitors, some of which may alter PARP-1-dependent gene regulatory programs to promote therapeutic outcomes.

Keywords: ADP-ribosylation; ARTD1; Activity; Chromatin; Gene expression; PARP-1; Poly(ADP-ribose); Posttranslational modification; Regulation; Transcription.

Publication types

  • Review

MeSH terms

  • Animals
  • DNA Methylation
  • Gene Expression Regulation*
  • Gene Regulatory Networks*
  • Histones / metabolism
  • Humans
  • Organ Specificity
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Poly(ADP-ribose) Polymerases / metabolism*
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Protein Processing, Post-Translational

Substances

  • Histones
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Poly(ADP-ribose) Polymerases