A 360-kb interchromosomal duplication of the human HYDIN locus

被引:44
作者
Doggett, Norman A.
Xie, Gary
Meincke, Linda J.
Sutherland, Robert D.
Mundt, Mark O.
Berbari, Nicolas S.
Davy, Brian E.
Robinson, Michael L.
Rudd, M. Katharine
Weber, James L.
Stallings, Raymond L.
Han, Cliff
机构
[1] Los Alamos Natl Lab, DOE Joint Genome Inst, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
[3] Ohio State Univ, Childrens Res Inst, Div Mol & Human Genet, Columbus, OH 43205 USA
[4] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[5] Marshfield Med Res Fdn, Ctr Genet Med, Marshfield, WI 54449 USA
[6] Univ Texas, Hlth Sci Ctr San Antonio, Childrens Canc Res Inst, San Antonio, TX 78229 USA
关键词
segmental duplication; interchromosomal duplication; gene duplication; HYDIN gene; human chromosome 16; human chromosome 1;
D O I
10.1016/j.ygeno.2006.07.012
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 HYDIN gene located in human chromosome band 16q22.2 is a large gene encompassing 423 kb of genomic DNA that has been suggested as a candidate for an autosomal recessive form of congenital hydrocephalus. We have found that the human HYDIN locus has been very recently duplicated, with a nearly identical 360-kb paralogous segment inserted on chromosome 1q21.1. The duplication, among the largest interchromosomal segmental duplications described in humans, is not accounted for in the current human genome assembly and appears to be part of a greater than 550-kb contig that must lie within 1 of the 11 sequence gaps currently remaining in 1q21.1. Both copies of the HYDIN gene are expressed in alternatively spliced transcripts. Elucidation of the role of HYDIN in human disease susceptibility will require careful discrimination among the paralogous copies. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:762 / 771
页数:10
相关论文
共 37 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   An Alu transposition model for the origin and expansion of human segmental duplications [J].
Bailey, JA ;
Liu, G ;
Eichler, EE .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (04) :823-834
[3]   Recent segmental duplications in the human genome [J].
Bailey, JA ;
Gu, ZP ;
Clark, RA ;
Reinert, K ;
Samonte, RV ;
Schwartz, S ;
Adams, MD ;
Myers, EW ;
Li, PW ;
Eichler, EE .
SCIENCE, 2002, 297 (5583) :1003-1007
[4]   GeneWise and genomewise [J].
Birney, E ;
Clamp, M ;
Durbin, R .
GENOME RESEARCH, 2004, 14 (05) :988-995
[5]   Prediction of complete gene structures in human genomic DNA [J].
Burge, C ;
Karlin, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :78-94
[6]  
CALLEN DF, 1990, CLIN GENET, V38, P466
[7]   Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence [J].
Cheung, J ;
Estivill, X ;
Khaja, R ;
MacDonald, JR ;
Lau, K ;
Tsui, LC ;
Scherer, SW .
GENOME BIOLOGY, 2003, 4 (04)
[8]   Finishing the euchromatic sequence of the human genome [J].
Collins, FS ;
Lander, ES ;
Rogers, J ;
Waterston, RH .
NATURE, 2004, 431 (7011) :931-945
[9]   Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene [J].
Davy, BE ;
Robinson, ML .
HUMAN MOLECULAR GENETICS, 2003, 12 (10) :1163-1170
[10]   Recent duplication, domain accretion and the dynamic mutation of the human genome [J].
Eichler, EE .
TRENDS IN GENETICS, 2001, 17 (11) :661-669