Allele specificity of DNA replication timing in the Angelman/Prader–Willi syndrome imprinted chromosomal region (original) (raw)
Nakamura, H., Morita, T. & Sato, C. Structural Organization of Replicon Domains during DMA Synthetic Phase in the Mammalian Nucleus. Exp. Cell Res.165, 291–297 (1986). ArticleCASPubMed Google Scholar
Nakayasu, H. & Berezney, R. Mapping Replicational Sites in the Eucaryotic cell Nucleus. J. Cell Biol.108, 1–11 (1989). ArticleCASPubMed Google Scholar
Fox, M.H., Arndt-Jovin, D.J., Jovin, T., Baumann, P.H. & Robert-Nicoud, M. Spatial and temporal distribution of DNA replication sites localized by immunofluorescence and confocal microscopy in mouse fibroblasts. J. Cell Sci.99, 247–253 (1991). PubMed Google Scholar
O'Keefe, R.T., Henderson, S.C. & Spector, D.L. Dynamic Organization of DNA replication in Mammalian Cell Nuclei: Spatially and Temporally Defined Replication of Chromosome-specific-α-Satellite DNA sequences. J. Cell Biol.116, 1095–1110 (1992). ArticleCASPubMed Google Scholar
Drouin, R., Lemieux, N. & Richer, C.-L. Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution. Chromosoma99, 273–280 (1990). ArticleCASPubMed Google Scholar
Latt, S.A. Miorofluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. Proc. natn. Acad. Sci. U.S.A.70, 3395–3399 (1973). ArticleCAS Google Scholar
Dutrillaux, B., Couturier, J., Richer, C.-L. & Viegas-Péquignot, E. Sequence of DNA replication in 227 R-and Q-bands of human chromosomes using a BrdU treatment. Chmmosoma58, 51–61 (1976). ArticleCAS Google Scholar
Edenberg, H.J. & Huberman, J.A. Eucaryotic chromosome replication. Ann. Rev. Genet.9, 245–284 (1975). ArticleCASPubMed Google Scholar
Hand, R. Eucaryotic DNA: Organization of the genome for replication. Cell15, 317–325 (1978). ArticleCASPubMed Google Scholar
Willard, H.F. & Latt, S.A. Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. Am. J. hum. Genet.28, 213–227 (1976). CASPubMedPubMed Central Google Scholar
Goldman, M.A., Holmquist, G.P., Gray, M.C., Caston, L.A. & Nag, A. Replication timing of mammalian genes and middle repetitive sequences. Science224, 686–692 (1984). ArticleCASPubMed Google Scholar
Hatton, K.S. et al. Replication program of active and inactive multigene families in mammalian cells. Molec. Cell. Biol.8, 2149–2158 (1988). ArticleCASPubMedPubMed Central Google Scholar
Dhar, V., Skoultchi, A.I. & Schildkraut, C.L. Activation and repression of a β-globin gene in cell hybrids is accompanied by a shift in its temporal replication. Molec. Cell. Biol.9, 3524–3532 (1989). ArticleCASPubMedPubMed Central Google Scholar
Izumikawa, Y., Naritomi, K. & Hirayama, K. Replication asynchrony between homologs 15q11.2: oytogenetic evidence for genomic imprinting. Hum. Genet.87, 1–5 (1991). ArticleCASPubMed Google Scholar
Kitsberg, D. et al. Allele-specific replication timing of imprinted gene regions. Nature364, 459–463 (1993). ArticleCASPubMed Google Scholar
Ledbetter, D.H. et al. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. New Engl. J. Med.304, 325–329 (1981). ArticleCASPubMed Google Scholar
Nicholls, R.D., Knoll, J.H.M., Butler, M.G., Karam, S. & Lalande, M. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome. Nature342, 281–285 (1989). ArticleCASPubMedPubMed Central Google Scholar
Knoll, J.H.M. et al. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am. J. med. Genet.32, 285–290 (1989). ArticleCASPubMed Google Scholar
Malcolm, S. et al. Uniparental paternal disomy in Angelman's syndrome. Lancet337, 694–697 (1991). ArticleCASPubMed Google Scholar
Wagstaff, J. et al. Maternal but not paternal transmission of 15q11–13-linked nondeletion Angelman syndrome leads to phenotypic expression. Nature Genet.1, 291–294 (1992). ArticleCASPubMed Google Scholar
Ozcelik, T. et al. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nature Genet.2, 265–269 (1992). ArticleCASPubMed Google Scholar
Selig, S., Okumura, K., Ward, D.C. & Cedar, H. Delineation of DNA replication time zones by fluorescence in situ hybridization. EMBO J.11, 1217–1225 (1992). ArticleCASPubMedPubMed Central Google Scholar
Wagstaff, J. et al. Localization of the gene encoding the GABAA receptor β3 subunit to the Angelman/Prader-Willi region of human chromosome 15. Am. J. hum. Genet. 49, 330–337 (1991). CAS Google Scholar
Knoll, J.H.M. et al. FISH ordering of reference markers and of the gene for the α5 subunit of the γ-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions. Hum. molec. Genet.2, 183–189 (1993). ArticleCASPubMed Google Scholar
Sinnett, D. et al. High-resolution mapping of the gamma-aminobutyric acid receptor subunit β3 and α5 gene cluster on chromosome 15q11–q13 and localization of breakpoints in two Angelman syndrome patients. Am. J. hum. Genet.52, 1216–1229 (1993). CASPubMedPubMed Central Google Scholar
Gardner, J.M. et al. The mouse pink-eyed dilution gene: Association with human Prader-Willi and Angelman syndromes. Science257, 1121–1124 (1992). ArticleCASPubMed Google Scholar
Left, S.E. et al. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Wilii syndrome region. Nature Genet.2, 259–264 (1992). Article Google Scholar
Cattanach, B.M. et al. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nature Genet.2, 270–274 (1992). ArticleCASPubMed Google Scholar
Leffak, M. & James, C.D. Opposite replication polarity of the germ line c-myc gene in HeLa _Cell_s compared with that of two Burkitt lymphoma cell lines. Molec. Cell. Biol.9, 586–593 (1989). ArticleCASPubMedPubMed Central Google Scholar
Fangman, W.L. & Brewer, B.J. A Question of Time: Replication Origins of Eukaryotic Chromosomes. Cell71, 363–366 (1992). ArticleCASPubMed Google Scholar
Hamabe, J. et al. DNA deletion and its parental origin in Angelman syndrome patients. Am. J. med. Genet.41, 64–68 (1991). ArticleCASPubMed Google Scholar
Saitoh, S. et al. Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene. Lancet339, 366–367 (1992). ArticleCASPubMed Google Scholar
Schanberg, L.E., Fleenor, D.E., Kurtzberg, J., Haynes, B.F. & Kaufman, R.E. Isolation and characterization of the genomic human CD7 gene: Structural similarity with the murine _Thy_−1 gene. Proc. natn. Acad. Sci. U.S.A.88, 603–607 (1991). ArticleCAS Google Scholar
Lawrence, J.B., Singer, R.H. & McNeil, J.A. Interphase and metaphase resolution of different distances within the human dystrophin gene. Science249, 928–932 (1990). ArticleCASPubMed Google Scholar