White as a reporter gene to detect transcriptional silencers specifying position-specific gene expression during Drosophila melanogaster eye development

Genetics. 1995 Nov;141(3):1075-86. doi: 10.1093/genetics/141.3.1075.

Abstract

The white+ gene was used as a reporter to detect transcriptional silencer activity in the Drosophila genome. Changes in the spatial expression pattern of white were scored in the adult eye as nonuniform patterns of pigmentation. Thirty-six independent P[lacW] transposant lines were collected. These represent 12 distinct pigmentation patterns and probably 21 loci. The spatial pigmentation pattern is due to cis-acting suppression of white+ expression, and the suppression probably depends on cell position rather than cell type. The mechanism of suppression differs from inactivation by heterochromatin. In addition, activation of lacZ in P[lacW] occurs also in specific patterns in imaginal discs and embryos in many of the lines. The expression patterns of white+ and lacZ may reflect the activity of regulatory elements belonging to an endogenous gene near each P[lacW] insertion site. We speculate that these putative POSE (position-specific expression) genes may have a role in pattern formation of the eye as well as other imaginal structures. Three of the loci identified are optomotor-blind, engrailed and invected. teashirt is also implicated as a candidate gene. We propose that this "silencer trap"' may be an efficient way of identifying genes involved in imaginal pattern formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters*
  • Animals
  • Drosophila Proteins*
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / growth & development
  • Eye / growth & development*
  • Eye Color / genetics
  • Eye Proteins*
  • Gene Expression Regulation, Developmental*
  • Genes, Reporter*
  • Genetic Complementation Test
  • Insect Hormones / biosynthesis
  • Insect Hormones / genetics*
  • Regulatory Sequences, Nucleic Acid*
  • Transcription, Genetic / genetics*

Substances

  • ATP-Binding Cassette Transporters
  • Drosophila Proteins
  • Eye Proteins
  • Insect Hormones
  • w protein, Drosophila