Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16

被引:48
作者
Le Saux, O
Urban, Z
Göring, HHH
Csiszar, K
Pope, FM
Richards, A
Pasquali-Ronchetti, I
Terry, S
Bercovitch, L
Lebwohl, MG
Breuning, M
van den Berg, P
Kornet, L
Ott, J
de Jong, PTVM
Bergen, AAB
Boyd, CD
机构
[1] Univ Hawaii, Pacific Biomed Res Ctr, Lab Matrix Pathobiol, Honolulu, HI 96822 USA
[2] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[3] Univ Wales Hosp, Inst Med Genet, MRC, Connect Tissue Genet Grp, Cardiff CF4 4XN, S Glam, Wales
[4] Univ Cambridge, Dept Pathol, MRC, Connect Tissue Genet Grp, Cambridge CB2 1QP, England
[5] Univ Modena, Dept Biomed Sci, I-41100 Modena, Italy
[6] PXE Int Inc, Sharon, MA 02067 USA
[7] Brown Univ, Dept Dermatol, Providence, RI 02908 USA
[8] CUNY Mt Sinai Sch Med, Dept Dermatol, New York, NY 10029 USA
[9] Leiden Univ, Dept Human Genet, NL-2333 AL Leiden, Netherlands
[10] Univ Hosp St Radroud, Dept Neurol, NL-6500 MB Nymegen, Netherlands
[11] Univ Maastricht, Dept Med Physiol, NL-6200 MD Maastricht, Netherlands
[12] Rockefeller Univ, Lab Stat Genet, New York, NY 10021 USA
[13] Netherlands Ophthalm Res Inst, NL-1100 AC Amsterdam, Netherlands
关键词
D O I
10.1006/geno.1999.5925
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
We have performed linkage analysis on 21 families with pseudoxanthoma elasticum (PXE) using 10 polymorphic markers located on chromosome 16p13.1. The gene responsible for the PXE phenotype was localized to an 8-cM region of 16p13.1 between markers D16S500 and D16S3041 with a maximum lod score of 8.1 at a recombination fraction of 0.04 for marker D16S3017. The lack of any locus heterogeneity suggests that the major predisposing allele for the PXE phenotype is located in this region. Haplotype studies of a total of 36 PXE families identified several recombinations that further confined the PXE gene to a region (< 1 cM) between markers D16S3060 and D16S79. This PXE locus was identified within a single YAC clone and several overlapping BAC recombinants. From sequence analysis of these BAC recombinants, it is clear that the distance between markers D16S3060 and D16S79 is about 820 kb and contains a total of nine genes including three pseudogenes. We predict that mutations in one of the expressed genes in the locus will be responsible for the PXE phenotype in these families. (C) 1999 Academic Press.
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页码:1 / 10
页数:10
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