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Linkage analysis and identification of deletion in Alagille syndrome gene
Author(s) -
YUAN ZENGRONG,
KOHSAKA TAKAO,
KOBAYASHI NOBORU
Publication year - 1997
Publication title -
pediatrics international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.49
H-Index - 63
eISSN - 1442-200X
pISSN - 1328-8067
DOI - 10.1111/j.1442-200x.1997.tb03661.x
Subject(s) - medicine , alagille syndrome , linkage (software) , identification (biology) , genetic linkage , genetics , gene , computational biology , cholestasis , biology , botany
Alagille syndrome (AGS) is a genetic disease and the responsible gene has already been mapped at 20p12. To more accurately detect the region of the AGS gene on the linkage map of chromosome 20p, 14 yeast artificial chromosome (YAC) clones were screened to construct a YAC contig in the candidate region and 13 locus markers and 2 sequence‐tagged sites (STS) were ordered. Combining all of the analyses, a 1.3 Mb critical region from D20S507 to D20S61 for the AGS gene was identified. As the human Jagged 1 gene ( JAGI ) lies just in this region and is responsible for the AGS disease, the genomic DNA in an AGS family without a visible deletion were analyzed by single‐strand conformational polymorphism (SSCP) and direct DNA sequencing, and a 2‐bp (CT) deletion mutation at exon 26 of the JAGI was identified.