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 language | English (US) |
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Pages (from-to) | 9923-9927 |
Number of pages | 5 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 87 |
Issue number | 24 |
State | Published - 1990 |
Externally published | Yes |
Keywords
- Aberrant pre-mRNA splicing
- Dominant suppression of heterochromatic position effects
- Heterochromatin-associated protein