Primed in situ labeling technique for subtelomeric rearrangements in 70 children with idiopathic mental retardation

Hong Tian , Hui Yu , Siqing Fu , Runming Jin

Current Medical Science ›› 2011, Vol. 31 ›› Issue (6) : 834 -836.

PDF
Current Medical Science ›› 2011, Vol. 31 ›› Issue (6) : 834 -836. DOI: 10.1007/s11596-011-0686-7
Article

Primed in situ labeling technique for subtelomeric rearrangements in 70 children with idiopathic mental retardation

Author information +
History +
PDF

Abstract

Subtelomeric rearrangements contribute to idiopathic mental retardation (MR), but most children with idiopathic MR do not show any chromosome abnormalities with standard cytogenetic analysis. The primed in situ labeling (PRINS) technique, using an oligonucleotide primer complementary to the telemetric repeat sequences (TTAGGG), can identify chromosome telomeric abnormality (deletion) in idiopathic MR children. In this study, seventy children with idiopathic MR were enrolled and subjected to PRINS. The results showed normal karyotype in all the children, subtelomeric rearrangements (1q del and 4q del) in 2 cases, which was confirmed by fluorescence in situ hybridization (FISH). It was concluded that PRINS is effective for the detection of subtelomeric rearrangements and may become a routine technique for cytogenetical abnormality screening.

Keywords

primed in situ labeling / fluorescence in situ hybridization / idiopathic mental retardation

Cite this article

Download citation ▾
Hong Tian, Hui Yu, Siqing Fu, Runming Jin. Primed in situ labeling technique for subtelomeric rearrangements in 70 children with idiopathic mental retardation. Current Medical Science, 2011, 31(6): 834-836 DOI:10.1007/s11596-011-0686-7

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

FlintJ., WilkieA.O., BuckleV.J., et al.. The detection of submicroscopic chromosomal rearrangements in idiopathic mental retardation. Nat Genet, 1995, 9(2): 132-140

[2]

KnightS.J., ReganR., NicodA., et al.. Subtle chromosomal rearrangements in children with unexplained mental retardation. Lancet, 1999, 354(9191): 1676-1681

[3]

RiegelM., BaumerA., JamarM., et al.. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes. Hum Genet, 2001, 109(3): 286-294

[4]

DawsonA.J., PutnamS., SchultzJ., et al.. Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features. Clin Genet, 2002, 62(6): 488-494

[5]

NessG.O., LybækH., HougeG.. Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities. Am J Med Genet, 2002, 113(2): 125-136

[6]

KochJ.E., KølvraaS., PetersenK.B., et al.. Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ. Chromosoma, 1989, 98(4): 259-265

[7]

CoullinP., RoyL., PellestorF., et al.. PRINS, the other in situ DNA labeling method useful in cellular biology. Am J Med Genet, 2002, 107(2): 127-135

[8]

KrabchiK., LavoieJ., CoullinP., et al.. From the conception of the PRINS to its coronation. Med Sci (Paris), 2004, 20(4): 465-473

[9]

KochJ., HindkjaerJ., KølvraaS., et al.. Construction of a panel of chromosome-specific oligonucleotide probes (PRINSprimers) useful for the identification of individual human chromosomes in situ. Cytogenet Cell Genet, 1995, 71(2): 142-147

[10]

YanJ., ChenB.Z., BouchardE.F., et al.. The labeling efficiency of human telomeres is increased by double-strand PRINS. Chromosoma, 2004, 113(4): 204-209

[11]

RavnanJ.B., TepperbergJ.H., PapenhausenP., et al.. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities. J Med Genet, 2006, 43(6): 478-489

[12]

AhnJ.W., OgilvieC.M., WelchA., et al.. Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre. BMC Med Genet, 2007, 8: 9

[13]

ShaoL., ShawC.A., LuX.Y., et al.. Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases. Am J Med Genet A, 2008, 146A(17): 2242-2251

[14]

TherkelsenA.J., NielsenA., KochJ., et al.. Staining of human telomeres with primed in situ labeling (PRINS). Cytogenet Cell Genet, 1995, 68(1–2): 115-118

[15]

BolzánA.D., BianchiM.S.. Telomeres, interstitial telomeric repeat sequences, and chromosomal aberrations. Mutat Res, 2006, 612(3): 189-214

[16]

BonifacioS., CentroneC., Da PratoL., et al.. Use of primed in situ labeling (PRINS) for the detection of telomeric deletions associated with mental retardation. Cytogenet Cell Genet, 2001, 93(1–2): 16-18

[17]

KoolenD.A., NillesenW.M., VersteegM.H., et al.. Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA). J Med Genet, 2004, 41(12): 892-899

[18]

WuY., JiangY.W., WangX.Z., et al.. Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay. Chin J Pediatr (Chinese), 2007, 45(12): 906-911

[19]

LiR., ZhaoZ.Y., PaiS.. Chromosome subtelomeric analysis by FISH in patients with mental retardation. J Zhejiang Univ (Med Sci) (Chinese), 2004, 33(4): 349-352

AI Summary AI Mindmap
PDF

92

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/