X-linked juvenile retinoschisis: Localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC

被引:9
作者
Pawar, H
Bingham, EL
Hiriyanna, K
Segal, M
Richards, JE
Sieving, PA
机构
[1] UNIV MICHIGAN,WK KELLOGG EYE CTR,DEPT OPHTHALMOL,ANN ARBOR,MI 48105
[2] UNIV MICHIGAN,DEPT EPIDEMIOL,ANN ARBOR,MI 48109
关键词
eye disease; genetic markers; juvenile retinoschisis; X-chromosome;
D O I
10.1159/000154373
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We studied 17 pedigrees with 108 affected males with X-linked juvenile retinoschisis (RS; McKusick No. 31270) and have analyzed all of the known polymorphic markers in the RS region of Xp22.1-p22.2 between DXS987 and DXS41. By haplotype analyses we found 7 individuals who showed crossovers in this interval surrounding RS, We previously reported AFM291wf5 as the centromeric boundary, and this remains unchanged in the present study, A new recombination was identified on the telomeric side at (DXS1195, DXS418). Our data support the locus order Xpter - (DXS987, DXS207, DXS1053, DXS43) - (DXS1195, DXS418)- (RS, DXS257 DXS999) - (AFM291wf5, DXS443) - DXS1052 - (DXS1226, DXS274, DXS41) - Xcen; loci grouped in parentheses could not be mutually ordered by our genetic data, Physical mapping has indicated a distance of at most 900-1,000 kb between (DXS1195, DXS418) and AFM291wf5. No recombination was observed between RS and DXS257 which lies in our new interval of interest, but one critical individual was not informative with this marker. Our data now define the smallest RS inclusion interval. This interval is contained on a single YAC from which we have identified expressed sequences as candidate genes for RS.
引用
收藏
页码:329 / 335
页数:7
相关论文
共 21 条
[1]   REFINED LOCALIZATION OF THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS [J].
ALITALO, T ;
KRUSE, TA ;
DELACHAPELLE, A .
GENOMICS, 1991, 9 (03) :505-510
[2]  
ALITALO T, 1988, AM J HUM GENET, V43, P476
[3]   A 6-MB YAC CONTIG IN XP22.1-P22.2 SPANNING THE DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, AND PHKA2 GENES [J].
ALITALO, T ;
FRANCIS, F ;
KERE, J ;
LEHRACH, H ;
SCHLESSINGER, D ;
WILLARD, HF .
GENOMICS, 1995, 25 (03) :691-700
[4]   CONSTRUCTION OF A HIGH-RESOLUTION LINKAGE MAP FOR XP22.1-P22.2 AND REFINEMENT OF THE GENETIC LOCALIZATION OF THE COFFIN-LOWRY SYNDROME GENE [J].
BIANCALANA, V ;
TRIVIER, E ;
WEBER, C ;
WEISSENBACH, J ;
ROWE, PSN ;
ORIORDAN, JLH ;
PARTINGTON, MW ;
HEYBERGER, S ;
OUDET, C ;
HANAUER, A .
GENOMICS, 1994, 22 (03) :617-625
[5]   DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE DXS365, DXS443 AND DXS451 LOCI [J].
BROWNE, D ;
BARKER, D ;
LITT, M .
HUMAN MOLECULAR GENETICS, 1992, 1 (03) :213-213
[6]   ISOLATION, CHARACTERIZATION, AND PHYSICAL LOCALIZATION OF 33 HUMAN X-CHROMOSOME RFLP MARKERS [J].
DIETZBAND, JN ;
TURCO, AE ;
WILLARD, HF ;
VINCENT, A ;
SKOLNICK, MH ;
BARKER, DF .
CYTOGENETICS AND CELL GENETICS, 1990, 54 (3-4) :137-141
[7]   GENETIC-ANALYSIS OF NEW FRENCH X-LINKED JUVENILE RETINOSCHISIS KINDREDS USING MICROSATELLITE MARKERS CLOSELY LINKED TO THE RS LOCUS - FURTHER NARROWING OF THE RS CANDIDATE REGION [J].
DUMUR, V ;
TRIVIER, E ;
PUECH, B ;
PEUGNET, F ;
ZANLONGHI, X ;
HACHE, JC ;
HANAUER, A .
HUMAN GENETICS, 1995, 96 (01) :79-82
[8]   AN INTEGRATED PHYSICAL AND GENETIC-MAP OF A 35 MB REGION ON CHROMOSOME XP22.3-XP21.3 [J].
FERRERO, GB ;
FRANCO, B ;
ROTH, EJ ;
FIRULLI, BA ;
BORSANI, G ;
DELMASMATA, J ;
WEISSENBACH, J ;
HALLEY, G ;
SCHLESSINGER, D ;
CHINAULT, AC ;
ZOGHBI, HY ;
NELSON, DL ;
BALLABIO, A .
HUMAN MOLECULAR GENETICS, 1995, 4 (10) :1821-1827
[9]   X-LINKED RETINOSCHISIS [J].
GEORGE, NDL ;
YATES, JRW ;
MOORE, AT .
BRITISH JOURNAL OF OPHTHALMOLOGY, 1995, 79 (07) :697-702
[10]  
GEORGE NDL, 1995, X CHROM WORKSH BANFF