Common motifs shared by conserved enhancers of Drosophila midline glial genes

J Exp Zool B Mol Dev Evol. 2011 Jan 15;316(1):61-75. doi: 10.1002/jez.b.21382. Epub 2010 Nov 2.


Coding sequences are usually the most highly conserved sectors of DNA, but genomic regions controlling the expression pattern of certain genes can also be conserved across diverse species. In this study, we identify five enhancers capable of activating transcription in the midline glia of Drosophila melanogaster and each contains sequences conserved across at least 11 Drosophila species. In addition, the conserved sequences contain reiterated motifs for binding sites of the known midline transcriptional activators, Single-minded, Tango, Dichaete, and Pointed. To understand the molecular basis for the highly conserved genomic subregions within enhancers of the midline genes, we tested the ability of various motifs to affect midline expression, both individually and in combination, within synthetic reporter constructs. Multiple copies of the binding site for the midline regulators Single-minded and Tango can drive expression in midline cells; however, small changes to the sequences flanking this transcription factor binding site can inactivate expression in midline cells and activate expression in tracheal cells instead. For the midline genes described in this study, the highly conserved sequences appear to juxtapose positive and negative regulatory factors in a configuration that activates genes specifically in the midline glia, while maintaining them inactive in other tissues, including midline neurons and tracheal cells.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Biological Evolution
  • Conserved Sequence*
  • Drosophila / embryology
  • Drosophila / genetics*
  • Drosophila / metabolism*
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism*
  • Gene Expression Regulation / physiology
  • Genes, Reporter
  • Molecular Sequence Data
  • Neuroglia / metabolism*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism


  • Drosophila Proteins
  • Phosphoproteins