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.
MeSH Terms
Alleles
Amino Acid Sequence
Animals
Base Sequence
Blotting, Southern
Chromobox Protein Homolog 5
Chromosomal Proteins, Non-Histone/genetics
Cloning, Molecular
DNA/genetics,isolation & purification
Drosophila melanogaster/genetics
Gene Library
Heterochromatin/metabolism
Molecular Sequence Data
Mutation
Oligonucleotide Probes
Polymerase Chain Reaction
Restriction Mapping
Suppression, Genetic
Chemicals
Chromosomal Proteins, Non-Histone
Heterochromatin
Oligonucleotide Probes
Chromobox Protein Homolog 5
DNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Eissenberg J C
E. A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, MO 63104.
James T C
Foster-Hartnett D M
Hartnett T
Ngan V
Elgin S C
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