A novel pax-like protein involved in transcriptional activation of cyst wall protein genes in Giardia lamblia

J Biol Chem. 2010 Oct 15;285(42):32213-26. doi: 10.1074/jbc.M110.156620. Epub 2010 Aug 10.

Abstract

Giardia lamblia differentiates into infectious cysts to survive outside of the host. It is of interest to identify factors involved in up-regulation of cyst wall proteins (CWPs) during this differentiation. Pax proteins are important regulators of development and cell differentiation in Drosophila and vertebrates. No member of this gene family has been reported to date in yeast, plants, or protozoan parasites. We have identified a pax-like gene (pax1) encoding a putative paired domain in the G. lamblia genome. Epitope-tagged Pax1 localized to nuclei during both vegetative growth and encystation. Recombinant Pax1 specifically bound to the AT-rich initiator elements of the encystation-induced cwp1 to -3 and myb2 genes. Interestingly, overexpression of Pax1 increased cwp1 to -3 and myb2 gene expression and cyst formation. Deletion of the C-terminal paired domain or mutation of the basic amino acids of the paired domain resulted in a decrease of the transactivation function of Pax1. Our results indicate that the Pax family has been conserved during evolution, and Pax1 could up-regulate the key encystation-induced genes to regulate differentiation of the protozoan eukaryote, G. lamblia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Gene Expression Regulation
  • Giardia lamblia / cytology*
  • Giardia lamblia / genetics*
  • Giardia lamblia / metabolism
  • Giardia lamblia / pathogenicity
  • Humans
  • Microarray Analysis
  • Molecular Sequence Data
  • Paired Box Transcription Factors / genetics*
  • Paired Box Transcription Factors / metabolism*
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protozoan Proteins / genetics*
  • Protozoan Proteins / metabolism*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Sequence Alignment
  • Transcriptional Activation*

Substances

  • Paired Box Transcription Factors
  • Protein Isoforms
  • Protozoan Proteins
  • Recombinant Proteins