Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH

被引:81
作者
Joyce, CA [1 ]
Dennis, NR
Cooper, S
Browne, CE
机构
[1] Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
[2] Princess Anne Hosp, Wessex Clin Genet Serv, Southampton, Hants, England
关键词
D O I
10.1007/s004390100588
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The cause of mental retardation, present in approximately 3% of the population, is unexplained in the majority of cases. Recent reports have suggested that cryptic telomeric rearrangements resulting in segmental aneuploidy and gene-dosage imbalance might represent a significant cause of idiopathic mental retardation (IMR). Two groups of patients with unexplained developmental delay (unselected and selected) and a group of control individuals have been investigated to determine the frequency of submicroscopic telomeric rearrangements associated with IMR and the frequency within the normal population. In contrast to current thinking, our data have shown that true cryptic telomeric rearrangements are not a significant cause of IMR. No fully cryptic abnormalities were detected in our IMR groups, although a semi-cryptic unbalanced telomeric translocation was identified in one selected patient by high-resolution G-band analysis. This abnormality was confirmed and characterised by fluorescence in situ hybridisation (FISH) with telomere-specific probes. A further 13 cytogenetically detected subtle terminal rearrangements were characterised by using multi-telomere FISH. Seven of these had previously been reported as normal, three of which were shown to be interstitial deletions. These cases illustrate the importance of high-resolution analysis to exclude subtle but cytogenetically visible abnormalities prior to subtelomere FISH screening when determining the frequency of cryptic telomeric rearrangements. Unexpectedly, two cryptic telomeric abnormalities were detected among our control individuals, suggesting that submicroscopic telomeric abnormalities may be a not uncommon finding in the general population. Hence, our data have important implications when defining the significance of cryptic telomeric rearrangements detected during screening programmes.
引用
收藏
页码:440 / 451
页数:12
相关论文
共 69 条
  • [1] Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
    Amos-Landgraf, JM
    Ji, YG
    Gottlieb, W
    Depinet, T
    Wandstrat, AE
    Cassidy, SB
    Driscoll, DJ
    Rogan, PK
    Schwartz, S
    Nicholls, RD
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (02) : 370 - 386
  • [2] Anderlid B, 1999, AM J HUM GENET, V65, pA67
  • [3] [Anonymous], 1996, Nat Genet, V14, P86
  • [4] Bacino CA, 2000, AM J MED GENET, V92, P250
  • [5] Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance
    Barber, JCK
    Joyce, CA
    Collinson, MN
    Nicholson, JC
    Willatt, LR
    Dyson, HM
    Bateman, MS
    Green, AJ
    Yates, JRW
    Dennis, NR
    [J]. JOURNAL OF MEDICAL GENETICS, 1998, 35 (06) : 491 - 496
  • [6] Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level
    Barber, JCK
    Reed, CJ
    Dahoun, SP
    Joyce, CA
    [J]. HUMAN GENETICS, 1999, 104 (03) : 211 - 218
  • [7] Combined immunocytogenetic and molecular cytogenetic analysis of meiosis I human spermatocytes
    Barlow, AL
    Hulten, MA
    [J]. CHROMOSOME RESEARCH, 1996, 4 (08) : 562 - 573
  • [8] A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
    Bartsch, O
    Hinkel, GK
    Petersen, MB
    Konig, U
    Bugge, M
    Mikkelsen, M
    Avramopoulos, D
    Morris, M
    Antonarakis, SE
    [J]. HUMAN GENETICS, 1997, 100 (5-6) : 669 - 675
  • [9] DETECTION OF A SUBTLE REARRANGEMENT OF CHROMOSOME-22 USING MOLECULAR TECHNIQUES
    BIESECKER, LG
    ROSENBERG, M
    DZIADZIO, L
    LEDBETTER, DH
    NING, Y
    SARNESO, C
    ROSENBAUM, K
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (04): : 389 - 394
  • [10] BLOUIN JL, 1995, AM J HUM GENET, V57, P388