Webb G C, Baker R T, Fagan K, Board P G
Division of Clinical Sciences, John Curtin School of Medical Research, Australian National University, Canberra.
Am J Hum Genet. 1990 Feb;46(2):308-15.
The chromosomal location of the human ubiquitin genes has been evaluated by in situ hybridization. Because of the conservation of the ubiquitin sequence, coding-region probes cannot distinguish between specific ubiquitin genes and reveal ubiquitin sequences in a number of different chromosomal regions. The major sites of hybridization with a coding-region probe include 17p11.1-p12, 12p24.2-q24.32, and 2q21-q24, with weaker hybridization over 1p3, 1q4, 2q3, and 13q. Hybridization with a probe isolated from the UbB gene intron indicated that this gene is located within the region 17p11.1-17p12. This region showed the strongest hybridization with the coding-region probe and is presumably also the location of the duplicated UbB pseudogene.
已通过原位杂交评估了人类泛素基因的染色体定位。由于泛素序列的保守性,编码区探针无法区分特定的泛素基因,并且会在多个不同的染色体区域中显示泛素序列。与编码区探针杂交的主要位点包括17p11.1-p12、12p24.2-q24.32和2q21-q24,在1p3、1q4、2q3和13q上杂交较弱。与从UbB基因内含子分离的探针杂交表明,该基因位于17p11.1-17p12区域内。该区域与编码区探针显示出最强的杂交,大概也是重复的UbB假基因的位置。