Eissenberg J C, James T C, Foster-Hartnett D M, Hartnett T, Ngan V, Elgin S C
E. A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, MO 63104.
Proc Natl Acad Sci U S A. 1990 Dec;87(24):9923-7. doi: 10.1073/pnas.87.24.9923.
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.
我们在此报告,果蝇中编码异染色质特异性非组蛋白染色体蛋白HP - 1的基因中的一个点突变与位置效应斑驳的显性抑制相关。该突变是最后一个内含子第一个核苷酸处的G到A转换,导致HP - 1 mRNA的错误剪接。这表明异染色质特异性蛋白在与异染色质位置效应相关的基因抑制中起核心作用。