Organization of the human beta-adducin gene (ADD2)

被引:22
作者
Gilligan, DM
Lozovatsky, L
Silberfein, A
机构
[1] Yale University School of Medicine, Department of Internal Medicine, Section of Hematology, WWW403, New Haven, CT 06510
[2] Department of Internal Medicine, Section of Hematology, Yale University School of Medicine, New Haven
关键词
D O I
10.1006/geno.1997.4802
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 intron-exon organization of the human P-adducin gene (ADD2) has been determined from overlapping genomic clones. The gene spans over 100 kb on chromosome 2p13 and comprises 17 exons. Seven of the exons are identical in size to the corresponding exons of the cu-adducin gene (4p16.3), suggesting gene duplication. A 275-bp fragment 5' to exon 1 demonstrates strong promoter activity in a transient transfection assay. Within 333 bp 5' of the first exon can be found several putative transcription factor-binding sites: three SP1 sites, one GATA site, three MZF1 sites, one p300 site, and one c-Ets site. Alternatively spliced exons in the 3' region are described and contain distinct coding regions, stop codons, and 3'UTR, corresponding to previously published beta-adducin cDNA sequences beta-1 and beta-2. The alternative splice sites for the smallest adducin isoform, beta-3, are alternative donor and acceptor sites within exons 7 and 12. The most recently described isoform, beta-4, includes an alternative exon (exon 15) that results in a frame shift and early termination, Intron-exon splice sites are presented for all 17 exons and conform to the consensus sequences for mammalian splice sites. These results will be useful in further analysis of tissue-specific expression of adducin isoforms and in analysis of DNA from patients with diseases mapping to this region of chromosome 2. (C) 1997 Academic Press.
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页码:141 / 148
页数:8
相关论文
共 35 条
[1]   Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LCMD2B) on chromosome 2p [J].
Bashir, R ;
Keers, S ;
Strachan, T ;
PassosBueno, R ;
Zatz, M ;
Weissenbach, J ;
LePaslier, D ;
Meisler, M ;
Bushby, K .
GENOMICS, 1996, 33 (01) :46-52
[2]   LINKAGE OF MIYOSHI MYOPATHY (DISTAL AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY) LOCUS TO CHROMOSOME 2P12-14 [J].
BEJAOUI, K ;
HIRABAYASHI, K ;
HENTATI, F ;
HAINES, JL ;
BENHAMIDA, C ;
BELAL, S ;
MILLER, RG ;
MCKENNAYASEK, D ;
WEISSENBACH, J ;
ROWLAND, LP ;
GRIGGS, RC ;
MUNSAT, TL ;
BENHAMIDA, M ;
ARAHATA, K ;
BROWN, RH .
NEUROLOGY, 1995, 45 (04) :768-772
[3]  
BENNETT V, 1993, ANNU REV CELL BIOL, V9, P27, DOI 10.1146/annurev.cb.09.110193.000331
[4]  
BENNETT V, 1988, J BIOL CHEM, V263, P5860
[5]   2 POINT MUTATIONS WITHIN THE ADDUCIN GENES ARE INVOLVED IN BLOOD-PRESSURE VARIATION [J].
BIANCHI, G ;
TRIPODI, G ;
CASARI, G ;
SALARDI, S ;
BARBER, BR ;
GARCIA, R ;
LEONI, P ;
TORIELLI, L ;
CUSI, D ;
FERRANDI, M ;
PINNA, LA ;
BARALLE, FE ;
FERRARI, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3999-4003
[6]   ASSOCIATION OF THE ALPHA-ADDUCIN LOCUS WITH ESSENTIAL-HYPERTENSION [J].
CASARI, G ;
BARLASSINA, C ;
CUSI, D ;
ZAGATO, L ;
MUIRHEAD, R ;
RIGHETTI, M ;
NEMBRI, P ;
AMAR, K ;
GATTI, M ;
MACCIARDI, F ;
BINELLI, G ;
BIANCHI, G .
HYPERTENSION, 1995, 25 (03) :320-326
[7]  
CHAPLINE C, 1993, J BIOL CHEM, V268, P6858
[8]   DIFFERENT GENETIC REQUIREMENTS FOR ANTERIOR RNA LOCALIZATION REVEALED BY THE DISTRIBUTION OF ADDUCIN-LIKE TRANSCRIPTS DURING DROSOPHILA OOGENESIS [J].
DING, D ;
PARKHURST, SM ;
LIPSHITZ, HD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2512-2516
[9]   35H, A SEQUENCE ISOLATED AS A PROTEIN-KINASE-C BINDING-PROTEIN, IS A NOVEL MEMBER OF THE ADDUCIN FAMILY [J].
DONG, LQ ;
CHAPLINE, C ;
MOUSSEAU, B ;
FOWLER, L ;
RAMSAY, K ;
STEVENS, JL ;
JAKEN, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (43) :25534-25540
[10]   MODULATION OF SPECTRIN ACTIN ASSEMBLY BY ERYTHROCYTE ADDUCIN [J].
GARDNER, K ;
BENNETT, V .
NATURE, 1987, 328 (6128) :359-362