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Original Article

Genetics of Chromosome 11: Loci for Pediatric and Adult Malignancies, Developmental Disorders, and Other Diseases

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Pages 646-659 | Published online: 11 Jun 2009

References

  • Sulston J, Du Z, Thomas K. The C. eleguns genome sequencing project: A beginning. Nature 1992; 356: 37–41
  • Memam J, Ashburner M, Hartl D L. Toward cloning and mapping the genome of Drosophila. Science 1991; 254: 221–225
  • Van Heyningen V, Little P FR. Report of the fourth international workshop on human chromosome 11 mapping 1994. Cytogenet Cell Genet 1995; 69: 128–157
  • Van Heyningen V, Jones C. Report of the committee on the genetic constitution of chromosome 11. Chromosome Coordinating Meeting 1992. Genome Priority Reports 1993; 1: 365–401
  • Litt M, Kramer P, Hauge X Y. A microsatellite-based index map of human chromosome 11. Hum Mol Genet 1993; 2: 909–913
  • Waziri M, Patil S R, Hanson J W. Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr 1983; 102: 873–876
  • Turleau C, DeGrouchy J, Chavin-Colin F. Trisomy 11p15 and Beckwith-Wiedemann syndrome: A report of two cases. Hum Genet 1984; 67: 219–221
  • Aleck K, Williams I, Mongkolsmai C. Partial trisomy 11p with interatrial septal aneurysm: Case report and literature review. Ann Genet 1985; 28: 102–106
  • Koufos A, Grundy P, Morgan K. Familial Wiedernann-Beckwith syndrome and a second Wilms' tumor locus both map to 11p15.5. Am J Hum Genet 1989; 44: 711–719
  • Ping A J, Reeve A F, Law D J. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet 1989; 44: 720–723
  • Mannens M, Hoovers J M, Redeker B. Characterization of regions on human chromosome 11p involved in the development of Wilms' tumor associated congenital diseases: A model to study genomic imprinting in man. Cytogenet Cell Genet 1991; 58: 1967
  • Hoovers J, Dietrich A, Mannens M. Imprinting and Beckwith-Wiedemann syndrome. Lancet 1992; 339: 1228
  • Weksberg R, Teshima I, Williams B RG. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refined the localization and suggests the gene for BWS is imprinted. Hum Mol Genet 1993; 2: 549–556
  • Wiedemann H R. Complexe maliformation familial avec hernia oblicale et macroglossie. Un “syndrome nouveau.”. J Genet Hum 1964; 13: 223–225
  • Pelletier J, Munroe D, Housman D. Molecular genetics of Wilms' tumor. Genome Analysis: Genes and Phenotypes, Vol 3, KE Davies, SM Tilghman. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 1991; 135–169
  • Seizinger B, Klinger H PJ, Junien C. Report of the committee on chromosome and gene loss in human neoplasia. Cytogenet Cell Genet 1991; 58: 1080–1096
  • Sait S NI, Nowak N J, Singh-Kahlon P. Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5. Genes, Chromosomes Cancer 1994; 11: 97–105
  • Coppes M J, Bonetta L, Huang A. Loss of heterozygosity mapping in Wilms' tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination. Genes, Chromosomes Cancer 1993; 5: 326–334
  • Zhang Y, Tycho B. Monoallelic expression of the human H19 gene. Nature Genet 1992; 1: 40–44
  • Giannoukakis N, Deal C, Paquette J. Parental genomic imprinting of the human IGF2 gene. Nature Genet 1993; 4: 98–101
  • Ohlsson R, Nystrom A, Pfeifer-Ohlsson S. IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nature Genet 1993; 4: 94–97
  • Ogawa O, Eccles M R, Szeto J. Relaxation of insulin-lie growth factor Il gene imprinting implicated in Wilms' tumor. Nature 1993; 362: 749–751
  • Rainier S, Johnson L A, Dobry C J. Relaxation of imprinted genes in human cancer. Nature 1993; 362: 747–749
  • Wekesberg R, Shen D R, Fei Y L. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nature Genet 1993; 5: 143–149
  • Boehm T, Foroni L, Kaneko Y. The rhombotin family of cystiene-rich LIM-domain oncogenes: Distinct members are involved in T-cell translocations to human chromosomes 11p15 and 11p13. Proc Natl Acad Sci USA 1991; 88: 4367–4371
  • Call K M, Glaser T, Ito C Y. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 1990; 60: 509–520
  • Ton C CT, Hirvonen H, Miwa H. Positional cloning and characterization of a paired box-and homeobox-containing gene from the aniridia region. Cell 1991; 67: 3059–1074
  • Gessler M, Poustka A, Cavenee W. Homozygous deletion in Wilms' tumors of zinc-finger gene identified by chromosome jumping. Nature 1990; 343: 774–778
  • Varanasi R, Bardeesy N, Ghahremani M. Fine structure analysis of the WT1 gene in sporadic Wilms' tumors. Roc Natl Acad Sci USA 1994; 91: 3554–3558
  • Orita M, Iwahana H, Kanazawa H. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci USA 1989; 86: 2766–2770
  • Pelletier J, Bruening W, Kashtan C E. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 1991; 67: 437–447
  • Pelletier J, Bruening W, Li F P. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumor. Nature 1991; 353: 431
  • Davis L M, Stallard R, Thomas G H. Two anonymous DNA segments distinguish the Wilms' tumor and anirida loci. Science 1988; 241: 840–842
  • Mannens M, Bleeker-Wagemakers E M, Bliek J. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenet Cell Genet 1989; 52: 32–36
  • Davis A, Cowell J K. Mutations in the PAX6 gene in patients with hereditary aniridia. Hum Mol Genet 1993; 2: 2093–2097
  • Hanson I M, Seawright A, Hardman K. PAX6 mutations in aniridia. Hum Mol Genet 1993; 2: 915–920
  • Saccone S, DeSario A, Della Valle G. The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes. Proc Natl Acad Sci USA 1992; 89: 4913–4917
  • Larsson C, Skogseid B, Oberg K. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 1988; 332: 85–87
  • Junien C, Van Heyningen V. Report of the committee on the genetic constitution of chromosome 11. Cytogenet Cell Genet 1991; 58: 459–554
  • Mitelman F. Catalog of Chromosome Aberrations in Cancer, 4th ed. Alan R Liss, New York 1991
  • Marx J. How cells cycle toward cancer. Science 1994; 263: 319–320
  • Karlseder J, Zeillinger R, Schneeberger C. Patterns of DNA amplification at band q13 of chromosome 11 in human breast cancer. Genes, Chromosomes Cancer 1994; 9: 42–48
  • Szepetowski P, Nguyen C, Perucca-Lostanlen D. D11S146 and BCL1 are physically linked but can be discriminated by their amplification status in human breast cancer. Genomics 1991; 10: 410–416
  • Stone E M, Nichols B E, Streb L M. Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nature Genet 1992; 1: 246–250
  • Kimberling W J, Möller CG, Davenport S. Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11. Genomics 1992; 14: 988–994
  • Smith R JH, Lee E C, Kimberling W J. Localization of two genes for Usher syndrome type 1 to chromosome 11. Genomics 1992; 14: 995–1002
  • Li Y, Müller B, Fuhrmann C. The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533. Am J Hum Genet 1992; 51: 749–754
  • Stone E M, Kimura A E, Folk J C. Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopdthy to chromosome 11q13. Hum Mol Genet 1992; 9: 685–689
  • Boder E. 1985. Ataxia telangiectasia: An overview. Ataxia Telangiectasia: Genetics, Neuropathology and Immunology of a Degenerative Disease of Childhood, RA Gatti, M Swift. Alan R Liss, New York 1985; 1–63
  • Gatti R A, Berkel I, Boder E. Localization of an ataxia-tel-angiectasia gene to chromosome 11q22–23. Nature 1988; 336: 577–580
  • McConville C M, Formstone C J, Hernandez D. Fine mapping of the chromosome 11q22–23 region using PFGE, linkage and haplotype analysis: Localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, phi 2.22. Nucleic Acids Res 1990; 18: 4335–4343
  • McConville C M, Woods C G, Farrall M. Analysis of 7 polymorphic markers at chromosome 11q22–23 in 35 ataxia telangiectasia families: Further evidence of linkage. Hum Genet 1990; 85: 215–220
  • Ziv Y, Rotman G, Frydman M. The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23. Genomics 1991; 9: 373–375
  • Kapp L N, Painter R B. Stable radioresistance in ataxia-telangiectasia cells containing DNA from normal human cells. Int J Radial Biol 1989; 56: 667–675
  • Buckler A, Chang D D, Craw S L. Exon amplification: A strategy to isolate mammalian genes based on RNA splicing. Proc Natl Acad Sci USA 1991; 88: 4005–4009
  • Rommens J M, Lin B, Hutchinson G B. A transcription map of the region containing the Huntington disease gene. Hum Mol Genet 1993; 2: 901–907
  • Kaneko Y, Shikano T, Maseki N. Clinical characteristics of infant acute leukemia with or without 11q23 translocations. Leukemia 1988; 2: 672–676
  • Pui C-H, Behm F G, Raimondi S C. Secondary acute myeloid leukemia in children treated for acute lymphoid leukemia. N Engl J Med 1989; 321: 136–142
  • Pui C-H, Ribeiro R C, Hancock M L. Acute myeloid leukemias in children treated with epipodophyllotoxins for acute lymphoblastic leukemia. N Engl J Med 1991; 325: 1682–1687
  • Ziemin-van der Poel S, McCabe N R, Gill H J. ldentification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias. Proc Natl Acad Sci USA 1991; 88: 10735–10739
  • McCabe N R, Burnett R C, Gill H J. Cloning of cDNAs of the MLL gene that detect DNA rearrangements and altered RNA transcripts in human leukemia cells with 11q23 translocations. Proc Natl Acad Sci USA 1992; 89: 11794–11798
  • Gu Y, Nakdmura T, Alder H. The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene. Cell 1992; 71: 701–708
  • Tkachuk D C, Kohler S, Cleary M L. Involvement of a homolog of drosophila trithorar by 11q23 chromosomal translocations in acute leukemias. Cell 1992; 71: 691–700
  • Lipinski M, Braham K, Philip I. Neuroectoderm-associated antigens on Ewing sarcoma cell lines. Cancer Res 1986; 47: 183–187
  • Turc-Carel C, Philip I, Berger M R. Chromosome study of Ewing's sarcoma (ES) cell lines: Consistency of a reciprocal translocation t(11;22)(q24;q12). Cancer Genet Cytogenet 1984; 12: 1–19
  • Delattre O, Zucman J, Plougaster B. Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumors. Nature 1992; 359: 162–165
  • O'Brien S J, Peters J, Searle A G. Report of the committee on comparative gene mapping, Human Genome Mapping Workshop, Japan 1993. Human Gene Mapping 1993, J Caticchia, P Pearson. Johns Hopkins Press, Baltimore, MD 1994; 846–892
  • Glaser T, Lane J, Housman D A. A mouse model of the aniridia-Wilms' tumor deletion syndrome. Science 1990; 250: 823–827
  • Matsuo T, Yamashitd-Osumi N, Noji S. A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cells. Nature Genet 1993; 3: 299–304
  • Green E D, Olson M V. Chromosomal region of the cystic fibrosis gene in yeast artificial chromosomes: A model for human genome mapping. Science 1990; 250: 94–98
  • Stanton VP, Jr, Aburatani H, Elango R. YAC isolation and contig assembly by hybridization of Alu-PCR products. Am J Hum Genet 1992; 51: A247
  • Richard CW, III, Boehnke M, Berg D J. A radiation hybrid map of the distal short arm of human chromosome 11 containing the Beckwith-Wiedemann and associated embryonal tumor disease loci. Am J Hum Genet 1993; 52: 915–921
  • Fan Y S, Davis L M, Shows T B. Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc Natl Acad Sci USA 1990; 87: 6223–6227
  • Qin S, Zhang J, Isaacs C. A chromosome 11 YAC library. Genomics 1993; 16: 580–585
  • Chumakov I, Rigault P, Guillou S. Continuum of overlapping clones spanning the entire human chromosome 21q. Nature 1992; 359: 380–387
  • Foote S, Vollrath D, Hilton A. The human Y chromosome: Overlapping DNA clones spanning the euchromatic region. Science 1992; 258: 60–66
  • Church D M, Stotler C J, Rutter J L. Isolation of genes from complex sources of mammalian genomic DNA using exon amplification. Nature Genet 1994; 6: 98–105
  • Grompe M. The rapid detection of unknown mutations in nucleic acids. Nature Genet 1993; 5: 111–117

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