The identification and localization of a human gene with sequence similarity to Polycomblike of Drosophila melanogaster

被引:44
作者
Coulson, M
Robert, S
Eyre, HJ
Saint, R [1 ]
机构
[1] Univ Adelaide, Dept Genet, Adelaide, SA 5005, Australia
[2] Womens & Childrens Hosp, Dept Cytogenet & Mol Genet, Ctr Med Genet, Adelaide, SA, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
D O I
10.1006/geno.1997.5201
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Drosophila Polycomb group (PcG) of genes is required for the epigenetic regulation of a number of important developmental genes, including the homeotic (Hox) genes. The members of this gene family encode proteins that do not share sequence similarity, implying that each plays a unique role in this epigenetic repression mechanism, Polycomblike (Pcl was the second PcG gene to be identified, We report here the isolation and characterization of a human cDNA, termed PHF1, which encodes a protein with significant sequence similarity to Drosophila Polycomblike (PCL). The region of similarity between PHF1 and PCL includes the two PHD fingers (C-4-H-C-3 motif), the region between them, and sequences C-terminal to the PHD fingers. PHF1 and PCL are 34% identical over this 258-residue region. PHF1 was mapped to 6p21.3 by fluorescence in situ hybridization, While several genetic diseases that are likely to result from developmental abnormalities map to this region, PHF1 is not a clear candidate gene for any of them, (C) 1998 academic Press.
引用
收藏
页码:381 / 383
页数:3
相关论文
共 22 条