Left-right axis asymmetry determining human Cryptic gene is transcriptionally repressed by Snail

BMC Dev Biol. 2016 Oct 28;16(1):39. doi: 10.1186/s12861-016-0141-x.

Abstract

Background: Establishment of the left-right axis is important for positioning organs asymmetrically in the developing vertebrate-embryo. A number of factors like maternally deposited molecules have emerged essential in initiating the specification of the axis; the downstream events, however, are regulated by signal-transduction and gene-expression changes identifying which remains a crucial challenge. The EGF-CFC family member Cryptic, that functions as a co-receptor for some TGF-beta ligands, is developmentally expressed in higher mammals and mutations in the gene cause loss or change in left-right axis asymmetry. Despite the strong phenotype, no transcriptional-regulator of this gene is known till date.

Results: Using promoter-analyses tools, we found strong evidence that the developmentally essential transcription factor Snail binds to the human Cryptic-promoter. We cloned the promoter-region of human Cryptic in a reporter gene and observed decreased Cryptic-promoter activation upon increasing Snail expression. Further, the expression of Cryptic is down-regulated upon exogenous Snail expression, validating the reporter assays and the previously identified role of Snail as a transcriptional repressor. Finally, we demonstrate using gel-shift assay that Snail in nuclear extract of PANC1 cells interacts with the promoter-construct bearing putative Snail binding sites and confirm this finding using chromatin immunoprecipitation assay.

Conclusions: Snail represses the expression of human Cryptic and therefore, might affect the signaling via Nodal that has previously been demonstrated to specify the left-right axis using the EGF-CFC co-receptors.

Keywords: Cryptic; EGF-CFC; Left-right-axis; Snail; Transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Body Patterning*
  • Cell Line
  • Cloning, Molecular
  • Embryonic Development
  • Gene Expression Regulation, Developmental
  • Genes, Reporter
  • HEK293 Cells
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Promoter Regions, Genetic*
  • Snail Family Transcription Factors / metabolism*
  • Transcription, Genetic

Substances

  • CFC1 protein, human
  • Intercellular Signaling Peptides and Proteins
  • SNAI1 protein, human
  • Snail Family Transcription Factors