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Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication

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Abstract

DNA replication kinetics of Prader-Willi/Angelman syndrome region of 15q11.2q12 was studied without synchronization in five human amniotic cell and five skin fibroblast strains with a marker 15 chromosome, i.e., 15p+ or der(15), as cytological marker to distinguish between the two homologs. BrdU-33258 Hoechst-Giemsa techniques were used to analyze and compare the late replication patterns in the 15q11.2q12 region between the homologs. Asynchronous replication between the homologs was observed in both amniocytes and fibroblasts. From cells of a marker 15 of known parental origin, the paternal 15q11.2q12 replicated earlier than that of the maternal 15 in 92%–95% of asynchronous metaphases. The remaining 5%–8% of asynchronous metaphases displayed maternal early/paternal late replication. This mosaic pattern of replication in the 15q11.2q12 region may be due to methylation mosaicism of genomic imprinting or a relative lack of self-control of replication. These results provide cytogenetic evidence of maternal imprinting and delayed replication in the 15q11.2q12 region.

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References

  • Bader S, Miller OJ, Mulkherzee BB (1963) Observation on chromosome duplication in cultured human leukocytes. Exp Cell Res 31:100–112

    Google Scholar 

  • Bird AP (1986) CpG-rich islands and the function of DNA methylation. Nature 321:209–213

    Google Scholar 

  • Cedar H (1988) DNA methylation and gene activity. Cell 53:3–4

    Google Scholar 

  • Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, Gillessen-Kaestbach G, Horsthemke B (1992) Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11–13. Hum Genet 90:313–315

    Google Scholar 

  • Donlon TA (1988) Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes. Hum Genet 80:322–328

    Google Scholar 

  • Driscoll DJ, Waters MF, Williams CA, Zori RT, Glenn CC, Avidano KM, Nicholls RD (1992) A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes. Genomics 13:917–924

    Google Scholar 

  • Dutrillaux B, Couturier J, Richer C-L, Viegas-Pequignot E (1976) Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment. Chromosoma 58:51–61

    Google Scholar 

  • Glenn CC, Nicholls RD, Robinson WP, Saithoh S, Niikawa N, Schinzel A, Horsthemke B, Driscoll DJ (1993) Modification of 15q11–q13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Hum Mol Genet 2: 1377–1382

    Google Scholar 

  • Grzeschik KH, Kim MA, Johannsmann R (1975) Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining. Humangenetik 29:41–59

    Google Scholar 

  • Hall JD (1990) Genomic imprinting. Arch Dis Child 65:1013–1016

    Google Scholar 

  • Holmquist GP (1987) Role of replication time in the control of tissue-specific gene expression. Am J Hum Genet 40:151–171

    Google Scholar 

  • ISCN (1985) An international system for human cytogenetic nomeclature. Harnden DG, Klinger HP (eds) Published in collaboration with Cytogenet Cell Genet. Karger, Basel

    Google Scholar 

  • Izumikawa Y, Naritomi K, Hirayama K (1991) Replication asynchrony between homologs 15q11.2: cytogenetic evidence for genomic imprinting. Hum Genet 87:1–5

    Google Scholar 

  • Kim MA, Johannsmann R, Grzeschik KH (1975) Giemsa staining of the sites replicating DNA early in human lymphocyte chromosomes. Cytogenet Cell Genet 15:363–371

    Google Scholar 

  • Kitsberg D, Selig S, Brandeis M, Simon I, Keshet I, Driscoll DJ, Nicholls RD, Cedar H (1993) Allele-specific replication timing of imprinted gene regions. Nature 364:459–463

    Google Scholar 

  • Knoll JHM, Nicholls RD, Magenis RE, Graham JM Jr, Lalande M, Latt SA (1989) Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of deletion. Am J Met Genet 32:285–290

    Google Scholar 

  • Knoll JHM, Wastaff J, Lalande M (1993) Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: An overview. Am J Met Genet 46:2–6

    Google Scholar 

  • Knoll JHM, Cheng S-D, Lalande M (1994) Allele specificity of DNA replication timing in Angelman/Prader-Willi syndrome imprinted chromosomal region. Nat Genet 6:41–46

    Google Scholar 

  • Latt SA (1975) Fluorescence analysis of late DNA replication in human metaphase chromosomes. Somat Cell Genet 1:293–321

    Google Scholar 

  • Ledbetter PH, Riccardi VM, Airhart SD, Strobel RJ, Keeman BS, Crawford JD (1981) Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med 304:325–329

    Google Scholar 

  • Lester SC, Korn NJ, Demars R (1982) Deregression of genes of the human X chromosome: evidence for differences in locus-specific rates of derepression and rates of transfer of active and inactive gene after DNA-mediated transformation. Somat Cell Genet 8:265–284

    Google Scholar 

  • Li E, Beard C, Jaenlsch R (1993) Role for DNA methylation in genomic imprinting. Nature 366:362–365

    Google Scholar 

  • Lin MS, Wilson MG (1983) The sequence of DNA replication in an isodicentric X chromosome in peripheral blood lymphocytes and skin fibroblasts from the same individual. Hum Genet 65: 139–143

    Google Scholar 

  • Lyon MF (1988) X-chromosome inactivation and the location and expression of X-linked gene. Am J Hum Genet 42:8–16

    Google Scholar 

  • Magenis RE, Toth-Fejel S, Allen LJ, Black M, Brown MG, Budden S, Cohen R, Friedman JM, Kalousek D, Zonana J, Lacy D, La Franchi S, Lahr M, Macfarlane J, Williams CPS (1990) Comparison of the 15q deletion in Prader-Willi and Angelman syndromes: specific region, extent of deletions, parental origin, and clinical consequences. Am J Med Genet 35:333–349

    Google Scholar 

  • Malcolm S, Clayton-Smith J, Nicholls M, Robb S, Webb T, Armour JAL, Jeffreys AJ, Pembrey ME (1991) Uniparental paternal disomy in Angelman's syndrome. Lancet 339:694–697

    Google Scholar 

  • McGowan R, Campbell R, Peterson A, Sapienza C (1989) Cellular mosaicism in the methylation and expression of hemizygous loci in the mouse. Genes Dev 3: 1669–1676

    Google Scholar 

  • Migeon BR (1991) Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa. Genet Res 56:91–98

    Google Scholar 

  • Mohandas T, Sparkes RS, Shapiro LJ (1981) Reactivation of an inactive human X chromosome: evidence for inactivation by DNA methylation. Science 211: 393–396

    Google Scholar 

  • Nicholls RD (1994) New insights reveal complex mechanisms involved in genomic imprinting. Am J Hum Genet 54:733–740

    Google Scholar 

  • Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M (1989) Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome. Nature 342:281–285

    Google Scholar 

  • Pembrey M, Fennell SJ, Van Den Berghe J, Fitchett M, Summers D, Butler L, Clark C, Griffiths M, Thompson E, Super M, Baraitser M (1989) The association of Angelman's syndrome with deletion within 15q11–13. J Med Genet 26:73–77

    Google Scholar 

  • Sandberg AA, Takagi N, Schmidt ML, Bross IJD (1968) Chronology and patterns of human chromosome replication. IX. Meta-synchronous DNA replication in homologs. Cytogenetics 7: 298–332

    Google Scholar 

  • Sapienza C, Tran TH, Paquette J, McGowan R, Peterson A (1989) A methylation mosaic model for mammalian genome imprinting. Prog Nucleic Acid Res Mol Biol 36: 145–157

    Google Scholar 

  • Silva AJ, White R (1988) Inheritance of allelic blueprints for methylation patterns. Cell 54: 142–152

    Google Scholar 

  • Toniolo D, Martin G, Migeon BR, Dono RC (1988) Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG clusters within 100 Kb of DNA. EMBO J 7:401–406

    Google Scholar 

  • Webb T (1992) Delayed replication of Xq27 in individuals with the fragile X syndrome. Am J Med Genet 43: 1057–1062

    Google Scholar 

  • Wolf SF, Migeon BR (1985) Clusters of CpG dinucleotides implicated by nuclease hyper-sensitivity as control elements of housekeeping gene. Nature 314:467–469

    Google Scholar 

  • Yu WD, Wengen SL, Steele MW (1990) X chromosome imprinting in fragile X syndrome. Hum Genet 85:590–594

    Google Scholar 

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Lin, M.S., Zhang, A. & Fujimoto, A. Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication. Hum Genet 96, 572–576 (1995). https://doi.org/10.1007/BF00197413

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  • DOI: https://doi.org/10.1007/BF00197413

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