Mutation in a heterochromatin-specific chromosomal protein is associated with suppression of position-effect variegation in Drosophila melanogaster

Joel C. Eissenberg, Tharappel C. James, Dawn M. Foster-Hartnett, Thomas Hartnett, Vivian Ngan, Sarah C.R. Elgin

Research output: Contribution to journalArticlepeer-review

481 Scopus citations

Abstract

We report here that a point mutation in the gene which encodes the heterochromatin-specific nonhistone chromosomal protein HP-1 in Drosophila melanogaster is associated with dominant suppression of position-effect variegation. The mutation, a G-to-A transition at the first nucleotide of the last intron, causes missplicing of the HP-1 mRNA. This suggests that heterochromatin-specific proteins play a central role in the gene suppression associated with heterochromatic position effects.

Original languageEnglish (US)
Pages (from-to)9923-9927
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume87
Issue number24
StatePublished - 1990
Externally publishedYes

Keywords

  • Aberrant pre-mRNA splicing
  • Dominant suppression of heterochromatic position effects
  • Heterochromatin-associated protein

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