Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes

被引:21
作者
Bowles, KR
Abraham, SE
Brugada, R
Zintz, C
Comeaux, J
Sorajja, D
Tsubata, S
Li, H
Brandon, L
Gibbs, RA
Scherer, SE
Bowles, NE
Towbin, JA
机构
[1] Baylor Coll Med, Dept Pediat Cardiol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Cardiovasc Sci, Houston, TX 77030 USA
[5] Toyama Med & Pharmaceut Univ, Dept Pediat, Toyama, Japan
基金
美国国家卫生研究院;
关键词
D O I
10.1006/geno.2000.6242
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
Dilated cardiomyopathy (DCM) is a major cause of morbidity and mortality and a leading cause of cardiac transplantation worldwide. Multiple loci and three genes encoding cardiac actin, desmin, and lamin A/C have been described for autosomal dominant DCM. Using recombination analysis, we have narrowed the 10q21-q23 locus to a region of approximately 4.1 cM. In addition, we have constructed a BAC contig, composed of 199 clones, which was used to develop a high-resolution physical map that contains the DCM critical region (approximately 3.9 Mb long). Seven genes, including ANX11, PPIF, DLG5, RPC155, RPS24, SFTPA1, and KCNMA1, have been mapped to the region of interest. RPC155, RPS24, SFTPA1, and KCNMA1 were excluded from further analysis based on their known functions and tissue-specific expression patterns. Mutational analysis of ANX11, DLG5, and PPIF revealed no disease-associated mutations. Multiple ESTs have also been mapped to the critical region. (C) 2000 Academic Press.
引用
收藏
页码:109 / 127
页数:19
相关论文
共 88 条
[41]   CHARACTERIZATION OF A 2ND HUMAN PULMONARY SURFACTANT-ASSOCIATED PROTEIN SP-A GENE [J].
KATYAL, SL ;
SINGH, G ;
LOCKER, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 6 (04) :446-452
[42]  
KEELING PJ, 1995, BRIT HEART J, V73, P417
[43]   CHARACTERIZATION OF TISSUE-EXPRESSED ALPHA-SUBUNITS OF THE HIGH-CONDUCTANCE CA2+-ACTIVATED K+ CHANNEL [J].
KNAUS, HG ;
EBERHART, A ;
KOCH, ROA ;
MUNUJOS, P ;
SCHMALHOFER, WA ;
WARMKE, JW ;
KACZOROWSKI, GJ ;
GARCIA, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (38) :22434-22439
[44]  
KRAJINOVIC M, 1995, AM J HUM GENET, V57, P846
[45]   The mitochondrial death/life regulator in apoptosis and necrosis [J].
Kroemer, G ;
Dallaporta, B ;
Resche-Rigon, M .
ANNUAL REVIEW OF PHYSIOLOGY, 1998, 60 :619-642
[46]   Desmin mutation responsible for idiopathic dilated cardiomyopathy [J].
Li, DX ;
Tapscoft, T ;
Gonzalez, O ;
Burch, PE ;
Quiñones, MA ;
Zoghbi, WA ;
Hill, R ;
Bachinski, LL ;
Mann, DL ;
Roberts, R .
CIRCULATION, 1999, 100 (05) :461-464
[47]   Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin [J].
Maeda, M ;
Holder, E ;
Lowes, B ;
Valent, S ;
Bies, RD .
CIRCULATION, 1997, 95 (01) :17-20
[48]   PREVALENCE AND ETIOLOGY OF IDIOPATHIC DILATED CARDIOMYOPATHY (SUMMARY OF A NATIONAL-HEART-LUNG-AND-BLOOD-INSTITUTE WORKSHOP) [J].
MANOLIO, TA ;
BAUGHMAN, KL ;
RODEHEFFER, R ;
PEARSON, TA ;
BRISTOW, JD ;
MICHELS, VV ;
ABELMANN, WH ;
HARLAN, WR .
AMERICAN JOURNAL OF CARDIOLOGY, 1992, 69 (17) :1458-1466
[49]  
Melberg A, 1999, ANN NEUROL, V46, P684, DOI 10.1002/1531-8249(199911)46:5<684::AID-ANA2>3.0.CO
[50]  
2-#