Evolutionary analysis of a cluster of ATP-binding cassette (ABC) genes

被引:44
作者
Annilo, T [1 ]
Chen, ZQ
Shulenin, S
Dean, M
机构
[1] NCI, Lab Genom Divers, Human Genet Sect, Frederick, MD 21702 USA
[2] NCI, Lab Genom Divers, SAIC Frederick, Intramural Res & Support Program, Frederick, MD 21702 USA
关键词
D O I
10.1007/s00335-002-2229-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To study the evolutionary history of ATP-binding cassette (ABC) transporters in mammals, we have characterized a cluster of five ABCA-subfamily genes localized on mouse Chromosome (Chr) 11. The genes, named Abca5, Abca6, Abca8a, Abca8b, and Abca9, are arranged in a head-to-tail fashion in a cluster that spans about 400 kb of the genomic DNA, each gene occupying about 70 kb. The transcripts of these genes contain an open reading frame from 4863 (for Abca8a and Abca8b) to 4929 for Abca5 nucleotides, and have distinct tissue-specific expression pattern. The predicted proteins contain two transmembrane domains and two nucleotide binding domains, arranged similar to the other members of ABCA subfamily. Similarity of both the genomic organization and primary structure among the genes in this cluster suggests that the duplications generating the cluster occurred relatively recently compared with most of the ABC genes in present-day mammalian genomes. For instance, the Fugu rubripes genome contains an ortholog for only one gene, Abca5, from this cluster. Phylogenetic and comparative sequence analysis reveals that after the divergence of rodent and primate lineages, at least one gene has been lost in each genome. In addition, we found that both mouse and human clusters show evidence of a number of gene conversions, in several cases involving intron sequences.
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页码:7 / 20
页数:14
相关论文
共 31 条
[1]   Simple and complex ABCR:: Genetic predisposition to retinal disease [J].
Allikmets, R .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) :793-799
[2]   A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy [J].
Allikmets, R ;
Singh, N ;
Sun, H ;
Shroyer, NE ;
Hutchinson, A ;
Chidambaram, A ;
Gerrard, B ;
Baird, L ;
Stauffer, D ;
Peiffer, A ;
Rattner, A ;
Smallwood, P ;
Li, YX ;
Anderson, KL ;
Lewis, RA ;
Nathans, J ;
Leppert, M ;
Dean, M ;
Lupski, JR .
NATURE GENETICS, 1997, 15 (03) :236-246
[3]  
Arnould I., 2001, GeneScreen, V1, P157, DOI DOI 10.1046/J.1466-920X.2001.00038.X
[4]   Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters [J].
Berge, KE ;
Tian, H ;
Graf, GA ;
Yu, LQ ;
Grishin, NV ;
Schultz, J ;
Kwiterovich, P ;
Shan, B ;
Barnes, R ;
Hobbs, HH .
SCIENCE, 2000, 290 (5497) :1771-1775
[5]   Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency [J].
Brooks-Wilson, A ;
Marcil, M ;
Clee, SM ;
Zhang, LH ;
Roomp, K ;
van Dam, M ;
Yu, L ;
Brewer, C ;
Collins, JA ;
Molhuizen, HOF ;
Loubser, O ;
Ouelette, BFF ;
Fichter, K ;
Ashbourne-Excoffon, KJD ;
Sensen, CW ;
Scherer, S ;
Mott, S ;
Denis, M ;
Martindale, D ;
Frohlich, J ;
Morgan, K ;
Koop, B ;
Pimstone, S ;
Kastelein, JJP ;
Genest, J ;
Hayden, MR .
NATURE GENETICS, 1999, 22 (04) :336-345
[6]   Membrane topology of the ATP binding cassette transporter ABCR and its relationship to ABC1 and related ABCA transporters -: Identification of N-linked glycosylation sites [J].
Bungert, S ;
Molday, LL ;
Molday, RS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :23539-23546
[7]   CPG ISLANDS AND GENES [J].
CROSS, SH ;
BIRD, AP .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1995, 5 (03) :309-314
[8]   The human ATP-binding cassette (ABC) transporter superfamily [J].
Dean, M ;
Rzhetsky, A ;
Allikmets, R .
GENOME RESEARCH, 2001, 11 (07) :1156-1166
[9]  
Deleuze JF, 1996, HEPATOLOGY, V23, P904, DOI 10.1053/jhep.1996.v23.pm0008666348
[10]   Detecting and characterizing gene conversions between multigene family members [J].
Drouin, G ;
Prat, F ;
Ell, M ;
Clarke, GDP .
MOLECULAR BIOLOGY AND EVOLUTION, 1999, 16 (10) :1369-1390