Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands

被引:7
作者
Colleaux, L
May, M
Belougne, J
Lepaslier, D
Schwartz, C
Fontes, M
机构
[1] GREENWOOD GENET CTR,GREENWOOD,SC 29646
[2] CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
关键词
Xq21; mental retardation; YAC contig;
D O I
10.1136/jmg.33.5.353
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic studies in families with X linked mental retardation have suggested the location of several MR genes in the human q21 region. Since the establishment of cloned resources is an essential step towards the cloning of genes involved in inherited diseases, we built a yeast artificial chromosome (YAC) contig and an STS map of this part of the X chromosome. The contig, which extends from PGK1 in Xq13.3 to DXS1002 in Xq21.2, consists of 30 YACs mapped with 21 markers and spans about 6 Mb. The YAC contig was used as a framework to localise several previously known genes and CEPH/Genethon polymorphic markers, as well as to construct a physical map of the region surrounding one of these genes. We recently localised a presumed MR locus to the region flanked by DXS233 (proximal) and CHM (distal). Tn the present work, the zinc finger gene, ZNF6, has been shown to lie within this region and to be highly expressed in brain, making it a good candidate MR gene. Similarly the VDAC1 gene has been mapped between DXS986 and DXS72 and its candidate gene status for the Allan-Herndon-Dudley syndrome is discussed.
引用
收藏
页码:353 / 357
页数:5
相关论文
共 29 条
[1]   PARACENTRIC INVERSION X(Q21.2Q24) ASSOCIATED WITH MENTAL-RETARDATION IN MALES AND NORMAL OVARIAN-FUNCTION IN FEMALES [J].
ABELIOVICH, D ;
DAGAN, J ;
KIMCHISARFATY, C ;
ZLOTOGORA, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 55 (03) :359-362
[2]   DEFINITION AND MAPPING OF STSS AT STR AND RFLP LOCI IN XP11-XQ22 [J].
BARKER, DF ;
FAIN, PR .
GENOMICS, 1993, 18 (03) :712-716
[3]   HUMAN GENES ENCODING THE VOLTAGE-DEPENDENT ANION CHANNEL (VDAC) OF THE OUTER MITOCHONDRIAL-MEMBRANE - MAPPING AND IDENTIFICATION OF 2 NEW ISOFORMS [J].
BLACHLYDYSON, E ;
BALDINI, A ;
LITT, M ;
MCCABE, ERB ;
FORTE, M .
GENOMICS, 1994, 20 (01) :62-67
[4]  
CARPENTER N J, 1988, American Journal of Human Genetics, V43, pA139
[5]   A 1ST-GENERATION PHYSICAL MAP OF THE HUMAN GENOME [J].
COHEN, D ;
CHUMAKOV, I ;
WEISSENBACH, J .
NATURE, 1993, 366 (6456) :698-701
[6]   PHYSICAL FINE MAPPING OF THE CHOROIDEREMIA LOCUS USING XQ21 DELETIONS ASSOCIATED WITH COMPLEX SYNDROMES [J].
CREMERS, FPM ;
VANDEPOL, DJR ;
DIERGAARDE, PJ ;
WIERINGA, B ;
NUSSBAUM, RL ;
SCHWARTZ, M ;
ROPERS, HH .
GENOMICS, 1989, 4 (01) :41-46
[7]  
CREMERS FPM, 1990, AM J HUM GENET, V47, P622
[8]   ASSOCIATION BETWEEN X-LINKED MIXED DEAFNESS AND MUTATIONS IN THE POU DOMAIN GENE POU3F4 [J].
DEKOK, YJM ;
VANDERMAAREL, SM ;
BITNERGLINDZICZ, M ;
HUBER, I ;
MONACO, AP ;
MALCOLM, S ;
PEMBREY, ME ;
ROPERS, HH ;
CREMERS, FPM .
SCIENCE, 1995, 267 (5198) :685-688
[9]  
FEINBERG AP, 1984, ANAL BIOCHEM, V137, P266
[10]   MUTATIONS IN A PUTATIVE GLOBAL TRANSCRIPTIONAL REGULATOR CAUSE X-LINKED MENTAL-RETARDATION WITH ALPHA-THALASSEMIA (ATR-X SYNDROME) [J].
GIBBONS, RJ ;
PICKETTS, DJ ;
VILLARD, L ;
HIGGS, DR .
CELL, 1995, 80 (06) :837-845