Supernumerary der(1) marker chromosome derived from a ring chromosome 1 which has retained the original centromere and euchromatin from 1q21.1→q21.3 with substantial loss of 1q12 heterochromatin in a female with dysmorphic features and psychomotoric developmental delay

被引:5
作者
Barbi, G [1 ]
Spaich, C
Adolph, S
Rossier, E
Kehrer-Sawatzki, H
机构
[1] Univ Ulm Klinikum, Abt Humangenet, D-89073 Ulm, Germany
[2] Olga Hosp, Inst Klin Genet, Stuttgart, Germany
关键词
marker chromosome; ring chromosome 1; pericentromeric chromatin;
D O I
10.1002/ajmg.a.30491
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a 5.5-year-old girl with dysmorphic features and psychomotoric developmental delay with a mitotically stable supernumerary marker chromosome. The origin of the marker was identified by microdissection and reverse painting of marker DNA as the pericentromeric region of chromosome 1. Fine mapping by FISH with selected YAC or BAC clones identified no p-arm material on the marker. The marker has retained its original centromere and euchromatin from 1q21.1-q21.3 but only small remnants of the 1q12 heterochromatin. Furthermore, some FISH clones presented single signals on the marker and others presented double signals indicating a partial duplication within the marker. These observations suggest a multi-step origin of the marker most probably with ring formation as the first step. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:419 / 424
页数:6
相关论文
共 21 条
[1]  
Anderlid BM, 2001, AM J MED GENET, V99, P223, DOI 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1146>3.0.CO
[2]  
2-W
[3]  
CALLEN DF, 1991, AM J HUM GENET, V48, P769
[4]  
Callen DF, 1999, J MED GENET, V36, P847
[5]   IDENTIFICATION OF SUPERNUMERARY RING CHROMOSOME-1 MOSAICISM USING FLUORESCENCE IN-SITU HYBRIDIZATION [J].
CHEN, H ;
TUCKMULLER, CM ;
BATISTA, DAS ;
WERTELECKI, W .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 56 (02) :219-223
[6]  
Crolla JA, 1998, AM J MED GENET, V75, P355, DOI 10.1002/(SICI)1096-8628(19980203)75:4<355::AID-AJMG4>3.0.CO
[7]  
2-P
[8]   Mosaic trisomy of a small r(1) with an abnormal phenotype [J].
Dawson, AJ ;
Konkin, D ;
Riordan, D ;
Chudley, AE .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 103 (01) :32-35
[9]   Masquerading repeats: Paralogous pitfalls of the human genome [J].
Eichler, EE .
GENOME RESEARCH, 1998, 8 (08) :758-762
[10]   FISH characterization of a supernumerary r(1)(::cen→q22::q22→sq21::) chromosome associated with multiple anomalies and bilateral cataracts [J].
Finelli, P ;
Cavalli, P ;
Giardino, D ;
Gottardi, G ;
Natacci, F ;
Savasta, S ;
Larizza, L .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 104 (02) :157-164