Fragile sites still breaking

被引:139
作者
Sutherland, GR [1 ]
Baker, E
Richards, RI
机构
[1] Womens & Childrens Hosp, Ctr Med Genet, Dept Cytogenet & Mol Genet, Adelaide, SA 5006, Australia
[2] Univ Adelaide, Dept Paediat, Adelaide, SA 5000, Australia
[3] Univ Adelaide, Dept Genet, Adelaide, SA 5000, Australia
关键词
D O I
10.1016/S0168-9525(98)01628-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rare fragile sites on chromosomes are the archetypal dynamic mutations. They involve large expansions of the microsatellite CCG or AT-rich minisatellites. The mutation process is an increase in repeat-unit number from within a normal range, through a premutation range, up to full mutation where the fragile site is expressed, Full mutations can inactivate genes and are regions of genomic instability. Common fragile sites in particular, might have a role in oncogenesis by facilitating gene inactivation through chromosomal deletion or amplification but this requires further exploration. The mechanisms behind the changes that give rise to the cytogenetic manifestation of chromosomal fragility are now beginning to be understood.
引用
收藏
页码:501 / 506
页数:6
相关论文
共 39 条
[1]  
BAKKER CE, 1994, CELL, V78, P23
[2]   Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B [J].
Boldog, F ;
Gemmill, RM ;
West, J ;
Robinson, M ;
Robinson, L ;
Li, EF ;
Roche, J ;
Todd, S ;
Waggoner, B ;
Lundstrom, R ;
Jacobson, J ;
Mullokandov, MR ;
Klinger, H ;
Drabkin, HA .
HUMAN MOLECULAR GENETICS, 1997, 6 (02) :193-203
[3]  
CHAKRABARTI L, 1996, GENOMICS, V44, P201
[4]  
Chan SY, 1998, CLIN GENET, V53, P179
[5]   In vitro reactivation of the FMR1 gene involved in fragile X syndrome [J].
Chiurazzi, P ;
Pomponi, MG ;
Willemsen, R ;
Oostra, BA ;
Neri, G .
HUMAN MOLECULAR GENETICS, 1998, 7 (01) :109-113
[6]   Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons [J].
Coquelle, A ;
Pipiras, E ;
Toledo, F ;
Buttin, G ;
Debatisse, M .
CELL, 1997, 89 (02) :215-225
[7]   Expansion and length-dependent fragility of CTG repeats in yeast [J].
Freudenreich, CH ;
Kantrow, SM ;
Zakian, VA .
SCIENCE, 1998, 279 (5352) :853-856
[8]   Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators [J].
Gecz, J ;
Bielby, S ;
Sutherland, GR ;
Mulley, JC .
GENOMICS, 1997, 44 (02) :201-213
[9]   Identification of the gene FMR2, associated with FRAXE mental retardation [J].
Gecz, J ;
Gedeon, AK ;
Sutherland, GR ;
Mulley, JC .
NATURE GENETICS, 1996, 13 (01) :105-108
[10]   Repeat expansion - All in a flap? [J].
Gordenin, DA ;
Kunkel, TA ;
Resnick, MA .
NATURE GENETICS, 1997, 16 (02) :116-118