Transcriptional regulation of human cyclic GMP-AMP synthase gene

Cell Signal. 2019 Oct:62:109355. doi: 10.1016/j.cellsig.2019.109355. Epub 2019 Jul 2.

Abstract

Cyclic GMP-AMP synthase (cGAS, cGAMP synthase) plays crucial roles in autoimmune disease, anti-tumor response, anti-senescence and anti-inflammatory response. Many studies have focused on cGAS-mediated signaling pathway. However, transcriptional mechanisms of cGAS gene have remained largely unknown. Here, we cloned the cGAS promoter region and characterized the molecular mechanisms controlling the cGAS transcriptional activity. By a series of 5' deletion and promoter constructions, we showed that the region (-414 to +76 relatives to the transcription start site) was sufficient for promoter activity. Mutation of Sp1 and CREB binding sites in this promoter region led to an apparent reduction of the cGAS promoter activity. Overexpression of Sp1 and CREB could obviously enhance promoter activity, whereas knocking-down of endogenous Sp1 and CREB markedly restrained the cGAS promoter activity. Sp1 and CREB binding to the cGAS promoter region in vivo was verified by Chromatin immunoprecipitation assay. These results pointed out that transcription factors Sp1 and CREB regulate the transcription of the cGAS gene.

Keywords: CREB; Sp1; Transcriptional regulation; cGAS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites / genetics
  • CREB-Binding Protein / genetics*
  • Chromatin Immunoprecipitation
  • Cloning, Molecular
  • Gene Expression Regulation
  • Humans
  • Nucleotidyltransferases / genetics*
  • Nucleotidyltransferases / isolation & purification
  • Promoter Regions, Genetic / genetics
  • Protein Binding / genetics
  • Signal Transduction / genetics
  • Sp1 Transcription Factor / genetics*
  • Transcription, Genetic*
  • Transcriptional Activation / genetics

Substances

  • Sp1 Transcription Factor
  • SP1 protein, human
  • CREB-Binding Protein
  • CREBBP protein, human
  • Nucleotidyltransferases
  • cGAS protein, human