PLoS ONE (Jan 2013)

PARP-14 binds specific DNA sequences to promote Th2 cell gene expression.

  • Jonathan P Riley,
  • Aishwarya Kulkarni,
  • Purvi Mehrotra,
  • Byunghee Koh,
  • Narayanan B Perumal,
  • Mark H Kaplan,
  • Shreevrat Goenka

DOI
https://doi.org/10.1371/journal.pone.0083127
Journal volume & issue
Vol. 8, no. 12
p. e83127

Abstract

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PARP-14, a member of the poly ADP-ribose polymerase super family, promotes T helper cell 2 (Th2) differentiation by regulating interleukin-4 (IL-4) and STAT6-dependent transcription. Yet, whether PARP-14 globally impacts gene regulation has not been determined. In this report, using an RNA pol II ChIP-seq approach, we identify genes in Th2 cells that are regulated by PARP-14, and either dependent or independent of ADP-ribosyltransferase catalytic activity. Our data demonstrate that PARP-14 enhances the expression of Th2 genes as it represses the expression of Th1-associated genes. Among the relevant targets are Signal Transducer and Activator of Transcription genes required for polarizing Th1 and Th2 cells. To define a mechanism for PARP-14 function, we use an informatics approach to identify putative PARP-14 DNA binding sites. Two putative PARP-14 binding motifs are identified in multiple Th2 cytokine genes, and we demonstrate that PARP-14 interacts with each motif using in vitro binding assays. Taken together our results indicate that PARP-14 is an important factor for T helper cell differentiation and it binds to specific DNA sequences to mediate its function.