Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q

被引:120
作者
Loftus, BJ
Kim, UJ
Sneddon, VP
Kalush, F
Brandon, R
Fuhrmann, J
Mason, T
Crosby, ML
Barnstead, M
Cronin, L
Mays, AD
Cao, YC
Xu, RX
Kang, HL
Mitchell, S
Eichler, EE
Harris, PC
Venter, JC
Adams, MD
机构
[1] Inst Genomic Res, Rockville, MD 20850 USA
[2] CALTECH, Div Biol, Pasadena, CA 91125 USA
[3] John Radcliffe Hosp, Mol Haematol Unit, Inst Mol Med, MRC, Oxford OX3 9DS, England
[4] Case Western Reserve Univ, Dept Genet, Cleveland, OH 44106 USA
关键词
D O I
10.1006/geno.1999.5927
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
Several publicly funded large-scale sequencing efforts have been initiated with the goal of completing the first reference human genome sequence by the year 2005. Here we present the results of analysis of 11.8 Mb of genomic sequence from chromosome 16. The apparent gene density varies throughout the region, but the number of genes predicted (84) suggests that this is a gene-poor region. This result may also suggest that the total number of human genes is likely to be at the lower end of published estimates. One of the most interesting aspects of this region of the genome is the presence of highly homologous, recently duplicated tracts of sequence distributed throughout the p-arm. Such duplications have implications for mapping and gene analysis as well as the predisposition to recurrent chromosomal structural rearrangements associated with genetic disease. (C) 1999 Academic Press.
引用
收藏
页码:295 / 308
页数:14
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