Adams D J, van der Weyden L, Kovacic A, Lovicu F J, Copeland N G, Gilbert D J, Jenkins N A, Ioannou P A, Morris B J
Gene Laboratory, Department of Physiology and Institute for Biomedical Research (F13), University of Sydney, Australia.
Cytogenet Cell Genet. 2000;88(1-2):68-73. doi: 10.1159/000015487.
The chromosome location and pattern of expression of the gene encoding the zinc finger protein 265 (alias "Zis") in human (ZNF265) and mouse (Zfp265) was determined. By interspecific backcross analysis, we mapped Zfp265 to mouse chromosome 3q. ZNF265 was localized to human chromosome 1p31 by fluorescence in situ hybridization. Since discovery of Zfp265 (in rat) came from studies of changes in renin expression in kidney cell lines, we examined the cell specificity of expression in kidney and also determined hybridization of cDNA with RNA in other tissues. We found that expression was not confined to renin mRNA-containing cells but was ubiquitous. Moreover, the fact that highly conserved homologs of ZNF265p exist in lower organisms (e.g., C4SR in Xenopus), suggests that this protein may have a generalized role in posttranscriptional mechanisms in various cell types and species.
确定了人类(ZNF265)和小鼠(Zfp265)中编码锌指蛋白265(别名“Zis”)的基因的染色体定位和表达模式。通过种间回交分析,我们将Zfp265定位到小鼠3号染色体的q臂。通过荧光原位杂交将ZNF265定位到人类1号染色体的p31区域。由于Zfp265(在大鼠中)的发现源于对肾细胞系中肾素表达变化的研究,我们研究了其在肾脏中的细胞表达特异性,并确定了cDNA与其他组织中RNA的杂交情况。我们发现其表达并不局限于含肾素mRNA的细胞,而是普遍存在的。此外,ZNF265p在低等生物(如非洲爪蟾中的C4SR)中存在高度保守的同源物,这表明该蛋白可能在各种细胞类型和物种的转录后机制中具有普遍作用。