The size, patterns in base composition and gene density, number and kind of genes, disease association and trisomy are compared in chromosomes 21 and 22.
Keywords: chromosome 21; chromosome 22; genomic sequence
Ian Dunham, The Sanger Institute, Hinxton, UK
Published online: September 2005
DOI: 10.1038/npg.els.0005015
The size, patterns in base composition and gene density, number and kind of genes, disease association and trisomy are compared in chromosomes 21 and 22.
Keywords: chromosome 21; chromosome 22; genomic sequence
| References | |
| Dawson E, Abecasis GR, Bumpstead S, et al. (2002) A first-generation linkage disequilibrium map of human chromosome 22. Nature 418: 544548. | |
| Dunham I, Hunt AR, Collins JE, et al. (1999) The DNA sequence of human chromosome 22. Nature 402: 489495; erratum Nature (2000) 404. | |
| Edelmann L, Pandita RK and Morrow BE (1999) Low-copy repeats mediate the common 3 Mb deletion in patients with velo-cardio-facial syndrome. American Journal of Human Genetics 64: 10761086. | |
| Edelmann L, Spiteri E, Koren K, et al. (2001) AT-rich palindromes mediate the constitutional t(11;22) translocation. American Journal of Human Genetics 68: 113. | |
| Hattori M, Fugiyama A, Taylor TD, et al. (2000) The DNA sequence of human chromosome 21. The chromosome 21 mapping and sequencing consortium. Nature 405: 311319. | |
| International Human Genome Sequencing Consortium (2001) Initial sequencing and analysis of the human genome. Nature 409: 860921. | |
| Patil N, Berno AJ, Hinds DA, et al. (2001) Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 294: 17191723. | |
| Sachidanandam R, Weissman D, Schmidt SC, et al. (2001) A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409: 928933. | |
| Shaikh TH, Kurahashi H and Emanuel BS (2001) Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review. Genetics in Medicine 3: 613. | |
| Wang SY, Cruts M, Del-Favero J, et al. (1999) A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes. Genome Research 9: 10591073. | |
| Further Reading | |
| Bailey JA, Gu Z, Clark RA, et al. (2002) Recent segmental duplications in the human genome. Science 297: 10031007. | |
| Bailey JA, Yavor AM, Viggiano L, et al. (2002) Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22. American Journal of Human Genetics 70: 83100. | |
| Collins JE, Goward ME, Cole CG, et al. (2003). Reevaluating human gene annotation: a second-generation alalysis of chromosome 22. Genome Research 13: 2736. | |
| Dawson E, Chen Y, Hunt S, et al. (2001) A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence. Genome Research 11: 170178. | |
| Kehrer-Sawatzki H, Wohr G, Schempp W, et al. (1998) Mapping of members of the low-copy-number repetitive DNA sequence family chAB4 within the p arms of human acrocentric chromosomes: characterization of Robertsonian translocations. Chromosome Research 6: 429435. | |
| Mullikin JC, Hunt SE, Cole CG, et al. (2000) An SNP map of human chromosome 22. Nature 407: 516520. | |
| Shiels C, Coutelle C and Huxley C (1997) Contiguous arrays of satellites 1, 3, and beta form a 1.5 Mb domain on chromosome 22p. Genomics 44: 3544. | |