Large-Scale Copy Number Polymorphism in the Human Genome

The extent to which large duplications and deletions contribute to human genetic variation and diversity is unknown. Here, we show that large-scale copy number polymorphisms (CNPs) (about 100 kilobases and greater) contribute substantially to genomic variation between normal humans. Representational oligonucleotide microarray analysis of 20 individuals revealed a total of 221 copy number differences representing 76 unique CNPs. On average, individuals differed by 11 CNPs, and the average length of a CNP interval was 465 kilobases. We observed copy number variation of 70 different genes within CNP intervals, including genes involved in neurological function, regulation of cell growth, regulation of metabolism, and several genes known to be associated with disease.

[1]  D. Tayloe,et al.  Pediatrics , 1927, The Indian Medical Gazette.

[2]  G. H. Bush,et al.  Pharmacogenetics , 1968 .

[3]  Aravinda Chakravarti,et al.  DNA duplication associated with Charcot-Marie-Tooth disease type 1A , 1991, Cell.

[4]  M. Wigler,et al.  Cloning the differences between two complex genomes , 1993, Science.

[5]  AC Tose Cell , 1993, Cell.

[6]  C. Disteche,et al.  DNA deletion associated with hereditary neuropathy with liability to pressure palsies , 1993, Cell.

[7]  B. Carritt,et al.  Lack of RH C/E expression in the Rhesus D– phenotype is the result of a gene deletion , 1994, Annals of human genetics.

[8]  M Ingelman-Sundberg,et al.  Frequent occurrence of CYP2D6 gene duplication in Saudi Arabians. , 1997, Pharmacogenetics.

[9]  K. Tanaka,et al.  TLE, the human homolog of groucho, interacts with AML1 and acts as a repressor of AML1-induced transactivation. , 1998, Biochemical and biophysical research communications.

[10]  R. Quatrano Genomics , 1998, Plant Cell.

[11]  J. Mason,et al.  Rab6c, a new member of the rab gene family, is involved in drug resistance in MCF7/AdrR cells. , 2000, Gene.

[12]  A. Zelenetz,et al.  Cloning and characterization of a Golgin-related gene from the large-scale polymorphism linked to the PML gene. , 2000, Genomics.

[13]  Jerzy K. Kulski,et al.  Comparative genomic analysis of the MHC: the evolution of class I duplication blocks, diversity and complexity from shark to man , 2002, Immunological Reviews.

[14]  D. Collier,et al.  A 3-Mb map of a large Segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14. , 2002, Genomics.

[15]  Herbert Herzog,et al.  Y4 receptor knockout rescues fertility in ob/ob mice. , 2002, Genes & development.

[16]  L. Barcellos,et al.  Gene copy number regulates the production of the human chemokine CCL3‐L1 , 2002, European journal of immunology.

[17]  M. Adams,et al.  Recent Segmental Duplications in the Human Genome , 2002, Science.

[18]  J. Sebat,et al.  Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation. , 2003, Genome research.

[19]  P. Buckland,et al.  Polymorphically duplicated genes: their relevance to phenotypic variation in humans , 2003, Annals of medicine.

[20]  J. Barber,et al.  Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster. , 2003, American journal of human genetics.

[21]  E. Eichler,et al.  Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome. , 2003, Genome research.

[22]  J. Clayton-Smith,et al.  Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport. , 2003, American journal of human genetics.

[23]  D. Cox,et al.  Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates. , 2003, Genome research.

[24]  J. Schwartz,et al.  Annotating large genomes with exact word matches. , 2003, Genome research.

[25]  Daniel Pinkel,et al.  Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization. , 2003, Genome research.

[26]  M Bobrow,et al.  Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features , 2004, Journal of Medical Genetics.

[27]  J. Lupski,et al.  Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease. , 2004, Human molecular genetics.

[28]  Bradley P. Coe,et al.  A tiling resolution DNA microarray with complete coverage of the human genome , 2004, Nature Genetics.

[29]  D. Hazuda,et al.  Integrase Inhibitors and Cellular Immunity Suppress Retroviral Replication in Rhesus Macaques , 2004, Science.

[30]  E. Eichler,et al.  BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications , 2004, Journal of Medical Genetics.

[31]  C. Glover,et al.  Gene expression profiling for hematopoietic cell culture , 2006 .

[32]  Synlett , 2022 .