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Volumn 64, Issue 2, 1999, Pages 354-359

Human genetics '99: Trinucleotide repeats: Fragile sites - Cytogenetic similarity with molecular diversity

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; BINDING SITE; CHROMOSOME FRAGILE SITE; CHROMOSOME FRAGILITY; DNA SEQUENCE; HUMAN; REVIEW;

EID: 0033071493     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302267     Document Type: Article
Times cited : (32)

References (36)
  • 2
    • 0031927129 scopus 로고    scopus 로고
    • Aberrant transcripts of the FHIT gene are expressed in normal and leukaemic haemopoietic cells
    • Carapeti M, Aguiar RC, Sill H, Goldman JM, Cross NC (1998) Aberrant transcripts of the FHIT gene are expressed in normal and leukaemic haemopoietic cells. Br J Cancer 78: 601-605
    • (1998) Br J Cancer , vol.78 , pp. 601-605
    • Carapeti, M.1    Aguiar, R.C.2    Sill, H.3    Goldman, J.M.4    Cross, N.C.5
  • 3
    • 0032132806 scopus 로고    scopus 로고
    • A new role for hypoxia in tumor progression: Induction of fragile site triggering genomic rearrangements and formation of complex DMs and HSRs
    • Coquelle A, Toledo F, Stern S, Bieth A, Debatisse M (1998) A new role for hypoxia in tumor progression: induction of fragile site triggering genomic rearrangements and formation of complex DMs and HSRs. Mol Cell 2:259-265
    • (1998) Mol Cell , vol.2 , pp. 259-265
    • Coquelle, A.1    Toledo, F.2    Stern, S.3    Bieth, A.4    Debatisse, M.5
  • 4
    • 0032471541 scopus 로고    scopus 로고
    • Molecular genetics of the calveolin gene family: Implications for human cancers, diabetes, Alzheimer disease, and muscular dystrophy
    • Engelman JA, Zhang X, Galbiati F, Volonte D, Sotgia F, Pestell RG, Minetti C, et al (1998a) Molecular genetics of the calveolin gene family: implications for human cancers, diabetes, Alzheimer disease, and muscular dystrophy. Am J Hum Genet 63:1578-1587
    • (1998) Am J Hum Genet , vol.63 , pp. 1578-1587
    • Engelman, J.A.1    Zhang, X.2    Galbiati, F.3    Volonte, D.4    Sotgia, F.5    Pestell, R.G.6    Minetti, C.7
  • 5
    • 0031758918 scopus 로고    scopus 로고
    • Genes encoding human caveolin-1 and -2 are co-localized to the D7S-522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers
    • Engelman JA, Zhang XL, Lisanti MP (1998b) Genes encoding human caveolin-1 and -2 are co-localized to the D7S-522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers. FEBS Lett 436:403-410
    • (1998) FEBS Lett , vol.436 , pp. 403-410
    • Engelman, J.A.1    Zhang, X.L.2    Lisanti, M.P.3
  • 6
    • 0031038239 scopus 로고    scopus 로고
    • Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype
    • Falik-Zaccai TC, Shachak E, Yalon M, Lis Z, Borochowitz Z, Macpherson JN, Nelson DL, et al (1997) Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype. Am J Hum Genet 60:103-112
    • (1997) Am J Hum Genet , vol.60 , pp. 103-112
    • Falik-Zaccai, T.C.1    Shachak, E.2    Yalon, M.3    Lis, Z.4    Borochowitz, Z.5    Macpherson, J.N.6    Nelson, D.L.7
  • 7
    • 0032488872 scopus 로고    scopus 로고
    • Expansion and length-dependent fragility of CTG repeats in yeast
    • Freudenreich CH, Kantrow SM, Zakian VA (1998) Expansion and length-dependent fragility of CTG repeats in yeast. Science 279:853-856
    • (1998) Science , vol.279 , pp. 853-856
    • Freudenreich, Ch.1    Kantrow, S.M.2    Zakian, V.A.3
  • 8
    • 0032538790 scopus 로고    scopus 로고
    • Targeted downregulation of caveolin-1 is sufficient to drive cell transformation and hyperactivate the p42/44 MAP kinase cascade
    • Galbiati F, Volonte D, Engelman JA, Watanabe G, Burk R, Pestell RG, Lisanti MP (1998) Targeted downregulation of caveolin-1 is sufficient to drive cell transformation and hyperactivate the p42/44 MAP kinase cascade. EMBO J 17: 6633-6648
    • (1998) EMBO J , vol.17 , pp. 6633-6648
    • Galbiati, F.1    Volonte, D.2    Engelman, J.A.3    Watanabe, G.4    Burk, R.5    Pestell, R.G.6    Lisanti, M.P.7
  • 9
    • 7844247606 scopus 로고    scopus 로고
    • Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1
    • Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, et al (1998) Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1 Hum Mol Genet 7:1935-1946
    • (1998) Hum Mol Genet , vol.7 , pp. 1935-1946
    • Gunter, C.1    Paradee, W.2    Crawford, D.C.3    Meadows, K.A.4    Newman, J.5    Kunst, C.B.6    Nelson, D.L.7
  • 10
    • 0030894828 scopus 로고    scopus 로고
    • A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication
    • Hansen RS, Canfield TK, Fjeld AD, Mumm S, Laird CD, Gartler SM (1997) A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication. Proc Natl Acad Sci USA 94:4587-4592
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 4587-4592
    • Hansen, R.S.1    Canfield, T.K.2    Fjeld, A.D.3    Mumm, S.4    Laird, C.D.5    Gartler, S.M.6
  • 11
    • 0032059864 scopus 로고    scopus 로고
    • FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis
    • Hewett DR, Handt O, Hobson L, Mangelsdorf M, Eyre H, Baker E, Sutherland GR, et al (1998) FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. Mol Cell 1:773-781
    • (1998) Mol Cell , vol.1 , pp. 773-781
    • Hewett, D.R.1    Handt, O.2    Hobson, L.3    Mangelsdorf, M.4    Eyre, H.5    Baker, E.6    Sutherland, G.R.7
  • 12
    • 0028133504 scopus 로고
    • Precursor arrays for triplet repeat expansion at the fragile X locus
    • Hirst MC, Grewal PK, Davies KE (1994) Precursor arrays for triplet repeat expansion at the fragile X locus. Hum Mol Genet 3:1553-1560
    • (1994) Hum Mol Genet , vol.3 , pp. 1553-1560
    • Hirst, M.C.1    Grewal, P.K.2    Davies, K.E.3
  • 13
    • 0031892622 scopus 로고    scopus 로고
    • Fish mapping of YAC clones at human chromosomal band 7q31.2: Identification of YACs spanning FRA7G within the common region of LOH in breast and prostate cancer
    • Huang H, Qian C, Jenkins RB, Smith DI (1998) Fish mapping of YAC clones at human chromosomal band 7q31.2: identification of YACs spanning FRA7G within the common region of LOH in breast and prostate cancer. Genes Chromosom Cancer 21:152-159
    • (1998) Genes Chromosom Cancer , vol.21 , pp. 152-159
    • Huang, H.1    Qian, C.2    Jenkins, R.B.3    Smith, D.I.4
  • 16
    • 0028896099 scopus 로고
    • Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
    • Jones C, Penny L, Mattina T, Yu S, Baker E, Voullaire L, Langdon WY, et al (1995) Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2. Nature 376:145-149
    • (1995) Nature , vol.376 , pp. 145-149
    • Jones, C.1    Penny, L.2    Mattina, T.3    Yu, S.4    Baker, E.5    Voullaire, L.6    Langdon, W.Y.7
  • 17
    • 0031924605 scopus 로고    scopus 로고
    • Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: Implications for the mechanism of fragile site induction
    • Le Beau MM, Rassool FV, Neilly ME, Espinosa R, III, Glover TW, Smith DI, McKeithan TW (1998) Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction. Hum Mol Genet 7:755-761
    • (1998) Hum Mol Genet , vol.7 , pp. 755-761
    • Le Beau, M.M.1    Rassool, F.V.2    Neilly, M.E.3    Espinosa R. III4    Glover, T.W.5    Smith, D.I.6    McKeithan, T.W.7
  • 18
    • 0031980212 scopus 로고    scopus 로고
    • A tandem array of minimal U1 small nuclear RNA genes is sufficient to generate a new adenovirus type 12-inducible chromosome fragile site
    • Li Z, Bailey AD, Buchowski J, Weiner AM (1998) A tandem array of minimal U1 small nuclear RNA genes is sufficient to generate a new adenovirus type 12-inducible chromosome fragile site. J Virol 72:4205-4211
    • (1998) J Virol , vol.72 , pp. 4205-4211
    • Li, Z.1    Bailey, A.D.2    Buchowski, J.3    Weiner, A.M.4
  • 20
    • 13144283613 scopus 로고    scopus 로고
    • Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site
    • Mishmar D, Rahat A, Scherer SW, Nyakatura G, Hinzmann B, Kohwi Y, Mandel-Gutfroind Y, et al (1998) Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proc Natl Acad Sci USA 14:8141-8146
    • (1998) Proc Natl Acad Sci USA , vol.14 , pp. 8141-8146
    • Mishmar, D.1    Rahat, A.2    Scherer, S.W.3    Nyakatura, G.4    Hinzmann, B.5    Kohwi, Y.6    Mandel-Gutfroind, Y.7
  • 24
    • 0031870490 scopus 로고    scopus 로고
    • Direct cloning and analysis of DNA sequences from a region of the Chinese hamster genome associated with aphidicolin-sensitive fragility
    • Palin AH, Critcher R, Fitzgerald DJ, Anderson JN, Farr CJ (1998) Direct cloning and analysis of DNA sequences from a region of the Chinese hamster genome associated with aphidicolin-sensitive fragility. J Cell Sci 111:1623-1634
    • (1998) J Cell Sci , vol.111 , pp. 1623-1634
    • Palin, A.H.1    Critcher, R.2    Fitzgerald, D.J.3    Anderson, J.N.4    Farr, C.J.5
  • 26
    • 0028242797 scopus 로고
    • Simple repeat DNA is not replicated simply
    • Richards RI, Sutherland GR (1994) Simple repeat DNA is not replicated simply. Nat Genet 6:114-116
    • (1994) Nat Genet , vol.6 , pp. 114-116
    • Richards, R.I.1    Sutherland, G.R.2
  • 27
    • 0026354010 scopus 로고
    • Selection in blood cells from female carriers of the fragile X syndrome: Inverse correlation between age and proportion of active X chromosomes carrying the full mutation
    • Rousseau F, Heitz D, Oberlé I, Mandel J-L (1991) Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation. J Med Genet 28: 830-836
    • (1991) J Med Genet , vol.28 , pp. 830-836
    • Rousseau, F.1    Heitz, D.2    Oberlé, I.3    Mandel, J.-L.4
  • 28
    • 0032514990 scopus 로고    scopus 로고
    • CTG repeats show bimodal amplification in E. Coli
    • Sarkar PS, Chang HC, Boudi FB, Reddy S (1998) CTG repeats show bimodal amplification in E. coli. Cell 95:531-540
    • (1998) Cell , vol.95 , pp. 531-540
    • Sarkar, P.S.1    Chang, H.C.2    Boudi, F.B.3    Reddy, S.4
  • 29
    • 0022495387 scopus 로고
    • The fragile site (16)(q22). I. Induction by AT-specific DNA-ligands and population frequency
    • Schmid M, Feichtinger W, Jessberger A, Köhler J, Lange R (1986) The fragile site (16)(q22). I. Induction by AT-specific DNA-ligands and population frequency. Hum Genet 74: 67-73
    • (1986) Hum Genet , vol.74 , pp. 67-73
    • Schmid, M.1    Feichtinger, W.2    Jessberger, A.3    Köhler, J.4    Lange, R.5
  • 30
    • 0033070196 scopus 로고    scopus 로고
    • Biological implications of the DNA structures associated with disease-causing triplet repeats
    • in this issue
    • Sinden RR (1999) Biological implications of the DNA structures associated with disease-causing triplet repeats. Am J Hum Genet 64:346-353 (in this issue)
    • (1999) Am J Hum Genet , vol.64 , pp. 346-353
    • Sinden, R.R.1
  • 32
    • 0022595330 scopus 로고
    • The most common fragile site in man is 3p14
    • Smeets DFCM, Scheres JMJC, Hustinx TWJ (1986) The most common fragile site in man is 3p14. Hum Genet 72: 215-220
    • (1986) Hum Genet , vol.72 , pp. 215-220
    • Dfcm, S.1    Jmjc, S.2    Hustinx, T.W.J.3
  • 33
    • 0001691881 scopus 로고
    • The enigma of the fragile X chromosome
    • Sutherland GR (1985) The enigma of the fragile X chromosome. Trends Genet 1:108-112
    • (1985) Trends Genet , vol.1 , pp. 108-112
    • Sutherland, G.R.1
  • 35
    • 0032401047 scopus 로고    scopus 로고
    • Fragile sites still breaking
    • _(1998) Fragile sites still breaking. Trends Genet 14: 501-506
    • (1998) Trends Genet , vol.14 , pp. 501-506
  • 36
    • 0030974861 scopus 로고    scopus 로고
    • Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
    • Yu S, Mangelsdorf M, Hewett D, Hobson L, Baker E, Eyre H, Lapsys N, et al (1997) Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat. Cell 88:367-374
    • (1997) Cell , vol.88 , pp. 367-374
    • Yu, S.1    Mangelsdorf, M.2    Hewett, D.3    Hobson, L.4    Baker, E.5    Eyre, H.6    Lapsys, N.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.