The DNA sequence and comparative analysis of human chromosome 5

被引:86
作者
Schmutz, J
Martin, J
Terry, A
Couronne, O
Grimwood, J
Lowry, S
Gordon, LA
Scott, D
Xie, G
Huang, W
Hellsten, U
Tran-Gyamfi, M
She, XW
Prabhakar, S
Aerts, A
Altherr, M
Bajorek, E
Black, S
Branscomb, E
Caoile, C
Challacombe, JF
Chan, YM
Denys, M
Detter, JC
Escobar, J
Flowers, D
Fotopulos, D
Glavina, T
Gomez, M
Gonzales, E
Goodstein, D
Grigoriev, I
Groza, M
Hammon, N
Hawkins, T
Haydu, L
Israni, S
Jett, J
Kadner, K
Kimball, H
Kobayashi, A
Lopez, F
Lou, YN
Martinez, D
Medina, C
Morgan, J
Nandkeshwar, R
Noonan, JP
Pitluck, S
Pollard, M
机构
[1] Stanford Univ, Sch Med, Stanford Human Genome Ctr, Dept Genet, Palo Alto, CA 94304 USA
[2] DOEs Joint Genome Inst, Walnut Creek, CA 94598 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[4] Lawrence Livermore Natl Lab, Livermore, CA 94550 USA
[5] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[6] Case Western Reserve Univ, Sch Med, Ctr Computat Genom, Dept Genet, Cleveland, OH 44106 USA
[7] Case Western Reserve Univ, Sch Med, Ctr Human Genet, Cleveland, OH 44106 USA
[8] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[9] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
D O I
10.1038/nature02919
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chromosome 5 is one of the largest human chromosomes and contains numerous intrachromosomal duplications, yet it has one of the lowest gene densities. This is partially explained by numerous gene-poor regions that display a remarkable degree of noncoding conservation with non-mammalian vertebrates, suggesting that they are functionally constrained. In total, we compiled 177.7 million base pairs of highly accurate finished sequence containing 923 manually curated protein-coding genes including the protocadherin and interleukin gene families. We also completely sequenced versions of the large chromosome-5-specific internal duplications. These duplications are very recent evolutionary events and probably have a mechanistic role in human physiological variation, as deletions in these regions are the cause of debilitating disorders including spinal muscular atrophy.
引用
收藏
页码:268 / 274
页数:7
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