Published online before print
February 12, 2003, 10.1101/gr.554603
Vol 13, Issue 3, 341-346, March 2003
Genomic DNA Insertions and Deletions Occur Frequently Between Humans and Nonhuman Primates
Kelly A. Frazer1,
Xiyin Chen,
David A. Hinds,
P.V. Krishna Pant,
Nila Patil and
David R. Cox
Perlegen Sciences, Mountain View, California 94043, USA
Comparative DNA sequence studies between humans and nonhuman
primates will be important for understanding the genetic basis of the
phenotypic differences between these species. Here we compare 27 Mb
of human chromosome 21 with chimpanzee DNA sequences identifying 57
genomic rearrangements (deletions and insertions ranging in size from
0.2 to 8.0 kb) between the two species. These rearrangements are
distributed along the entire length of chromosome 21, with 35%
found in genomic intervals encoding genes (genic intervals), and have
occurred in the genomes of both humans and chimpanzees. Comparison of
9 Mb of human chromosome 21 with orangutan, rhesus macaque, and
woolly monkey DNA sequences identified a combined total of 114 genomic
rearrangements between humans and nonhuman primates. Analysis of these
rearrangements revealed that they are randomly distributed with respect
to genic and nongenic intervals and identified one deletion that has
likely resulted in the inactivation of a gene
( 1,3-galactosyltransferase) in the woolly monkey. Our data show that
genomic rearrangements have occurred frequently during primate genome
evolution and significantly contribute to the DNA differences between
these species. These DNA rearrangements are commonly found in genic
intervals, and thus provide natural starting points for focused
investigations of qualitative and quantitative gene expression
differences between humans and other
primates.
[Supplemental material is available online at
www.genome.org.]
1 Corresponding author.
E-MAIL kelly_frazer{at}perlegen.com; FAX (650) 625-4510.
Article and publication are at
http://www.genome.org/cgi/doi/10.1101/gr.554603. Article published online before print in February
2003.

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
F.-C. Chen, C.-J. Chen, and T.-J. Chuang
INDELSCAN: a web server for comparative identification of species-specific and non-species-specific insertion/deletion events
Nucleic Acids Res.,
July 13, 2007;
35(suppl_2):
W633 - W638.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F.-C. Chen, C.-J. Chen, W.-H. Li, and T.-J. Chuang
Human-specific insertions and deletions inferred from mammalian genome sequences
Genome Res.,
January 1, 2007;
17(1):
16 - 22.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Pathak, S. Premi, J. Srivastava, S. P. Chandy, and S. Ali
Genomic Instability of the DYZ1 Repeat in Patients with Y Chromosome Anomalies and Males Exposed to Natural Background Radiation
DNA Res,
January 1, 2006;
13(3):
103 - 109.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Antonell, O. de Luis, X. Domingo-Roura, and L. A. Perez-Jurado
Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23
Genome Res.,
September 1, 2005;
15(9):
1179 - 1188.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. W. Karaman, S. Groshen, C.-C. Lee, B. L. Pike, and J. G. Hacia
Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays
Nucleic Acids Res.,
February 18, 2005;
33(3):
e33 - e33.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Stankiewicz, C. J. Shaw, M. Withers, K. Inoue, and J. R. Lupski
Serial segmental duplications during primate evolution result in complex human genome architecture
Genome Res.,
November 1, 2004;
14(11):
2209 - 2220.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Suzuki, R. Yamashita, M. Shirota, Y. Sakakibara, J. Chiba, J. Mizushima-Sugano, K. Nakai, and S. Sugano
Sequence Comparison of Human and Mouse Genes Reveals a Homologous Block Structure in the Promoter Regions
Genome Res.,
September 1, 2004;
14(9):
1711 - 1718.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Sebat, B. Lakshmi, J. Troge, J. Alexander, J. Young, P. Lundin, S. Maner, H. Massa, M. Walker, M. Chi, et al.
Large-Scale Copy Number Polymorphism in the Human Genome
Science,
July 23, 2004;
305(5683):
525 - 528.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. J. Shaw and J. R. Lupski
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease
Hum. Mol. Genet.,
April 1, 2004;
13(90001):
R57 - 64.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Nagpal, M. W. Karaman, M. M. Timmerman, V. V. Ho, B. L. Pike, and J. G. Hacia
Improving the sensitivity and specificity of gene expression analysis in highly related organisms through the use of electronic masks
Nucleic Acids Res.,
March 18, 2004;
32(5):
e51 - e51.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. A. Frazer, H. Tao, K. Osoegawa, P. J. de Jong, X. Chen, M. F. Doherty, and D. R. Cox
Noncoding Sequences Conserved in a Limited Number of Mammals in the SIM2 Interval are Frequently Functional
Genome Res.,
March 1, 2004;
14(3):
367 - 372.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|