THE IDURONATE SULFATASE GENE - ISOLATION OF A 1.2-MB YAC CONTIG SPANNING THE ENTIRE GENE AND IDENTIFICATION OF HETEROGENEOUS DELETIONS IN PATIENTS WITH HUNTER SYNDROME

被引:45
作者
PALMIERI, G
CAPRA, V
ROMANO, G
DURSO, M
JOHNSON, S
SCHLESSINGER, D
MORRIS, P
HOPWOOD, J
DINATALE, P
GATTI, R
BALLABIO, A
机构
[1] BAYLOR COLL MED,INST MOLEC GENET,HOUSTON,TX 77030
[2] WASHINGTON UNIV,SCH MED,DEPT MOLEC MICROBIOL,ST LOUIS,MO 63110
[3] WASHINGTON UNIV,SCH MED,CTR GENET MED,ST LOUIS,MO 63110
[4] ADELAIDE CHILDRENS HOSP INC,DEPT CHEM PATHOL,ADELAIDE,SA 5006,AUSTRALIA
[5] NAPLES UNIV,FAC MED 2,DEPT BIOCHEM & CHEM PATHOL,ADELAIDE,SA 5006,AUSTRALIA
[6] IST GIANNINA GASLINI,I-16148 GENOA,ITALY
关键词
D O I
10.1016/0888-7543(92)90405-H
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
A recently isolated cDNA clone from the iduronate sulfatase (IDS) gene has been used both to seed a contig of overlapping yeast artificial chromosomes (YACs) and to investigate the molecular defect in patients with Hunter syndrome (MPS II). Six YAC clones were found to span the IDS gene, and those and 14 other YACs were assembled into a 1.2-Mb contig around the gene in Xq27-q28. The physical map of the region identifies several putative CpG islands, suggesting the presence of other genes in the vicinity. DNA from a patient with a translocation breakpoint in the gene also permitted the orientation of the contig in the chromosome. Southern analysis of DNA from 25 unrelated Italian Hunter syndrome patients revealed 4 with deletions or rearrangements in the IDS gene. © 1992.
引用
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页码:52 / 57
页数:6
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