Identification and characterization of a novel gene (C4orf5) located on human chromosome 4q with specific expression in cardiac and skeletal muscle

被引:20
作者
Ahmad, F
Gonzalez, O
Ramagli, LO
Xu, JP
Siciliano, MJ
Bachinski, LL
Roberts, R
机构
[1] Baylor Coll Med, Dept Med, Cardiol Sect, Houston, TX 77030 USA
[2] Baylor Coll Med, DeBakey Heart Ctr, Grad Program Cardiovasc Sci, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
关键词
D O I
10.1006/geno.2000.6399
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
The loci of several genes responsible for arrhythmogenic right ventricular dysplasia (ARVD) have been mapped. Since ARVD involves the right ventricle, we sought candidate genes preferentially expressed in the right ventricle utilizing differential display polymerase chain reaction (PCR) on mRNA from the chambers of an adult human heart, PCR products were cloned, sequenced, and used to screen an adult heart cDNA library. A novel 1.3-kb cDNA (HG;MW-approved symbol C4orf5) with an open reading frame of 795 bp was identified. A probe designed from the 3' untranslated region of the 1.3-kb cDNA was hybridized to the 1.3-kb transcript and an alternatively spliced 2.5-kb transcript in the heart and skeletal muscle RNA lanes on a multitissue Northern blot. Analysis of a 39-kb partial genomic sequence identified three intronic splice sites in the 1.3-kb transcript. The gene was mapped to human chromosome 4q26-q27. Computer-based analysis indicated that this gene is novel with no known function. (C) 2000 Academic Press.
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页码:347 / 353
页数:7
相关论文
共 23 条
[11]   MOLECULAR CHARACTERIZATION OF 16P DELETIONS ASSOCIATED WITH INVERSION-16 DEFINES THE CRITICAL FUSION FOR LEUKEMOGENESIS [J].
MARLTON, P ;
CLAXTON, DF ;
LIU, P ;
ESTEY, EH ;
BERAN, M ;
LEBEAU, M ;
TESTA, JR ;
COLLINS, FS ;
ROWLEY, JD ;
SICILIANO, MJ .
BLOOD, 1995, 85 (03) :772-779
[12]   Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity [J].
Mestroni, L ;
Rocco, C ;
Gregori, D ;
Sinagra, G ;
Di Lenarda, A ;
Miocic, S ;
Vatta, M ;
Pinamonti, B ;
Muntoni, F ;
Caforio, ALP ;
McKenna, WJ ;
Falaschi, A ;
Giacca, M ;
Camerini, F .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 34 (01) :181-190
[13]   A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1Q42-Q43 [J].
RAMPAZZO, A ;
NAVA, A ;
ERNE, P ;
EBERHARD, M ;
VIAN, E ;
SLOMP, P ;
TISO, N ;
THIENE, G ;
DANIELI, GA .
HUMAN MOLECULAR GENETICS, 1995, 4 (11) :2151-2154
[14]   ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm [J].
Rampazzo, A ;
Nava, A ;
Miorin, M ;
Fonderico, P ;
Pope, B ;
Tiso, N ;
Livolsi, B ;
Zimbello, R ;
Thiene, G ;
Danieli, GA .
GENOMICS, 1997, 45 (02) :259-263
[15]   THE GENE FOR ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY MAPS TO CHROMOSOME 14Q23-Q24 [J].
RAMPAZZO, A ;
NAVA, A ;
DANIELI, GA ;
BUJA, G ;
DALIENTO, L ;
FASOLI, G ;
SCOGNAMIGLIO, R ;
CORRADO, D ;
THIENE, G .
HUMAN MOLECULAR GENETICS, 1994, 3 (06) :959-962
[16]  
SAMBROOK J, 1992, MOL CLONING LAB MANU
[17]  
SCHOTT JJ, 1995, AM J HUM GENET, V57, P1114
[18]  
Seidman CE, 1998, BASIC RES CARDIOL, V93, P13
[19]   A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14 [J].
Severini, GM ;
Krajinovic, M ;
Pinamonti, B ;
Sinagra, G ;
Fioretti, P ;
Brunazzi, MC ;
Falaschi, A ;
Camerini, F ;
Giacca, M ;
Mestroni, L .
GENOMICS, 1996, 31 (02) :193-200
[20]   SUDDEN UNEXPECTED NONTRAUMATIC DEATH IN 54 YOUNG-ADULTS - A 30-YEAR POPULATION-BASED STUDY [J].
SHEN, WK ;
EDWARDS, WD ;
HAMILL, SC ;
BAILEY, KR ;
BALLARD, DJ ;
GERSH, BJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 76 (03) :148-152