Molecular characterization of inv dup del(8p): Analysis of five cases

被引:56
作者
Shimokawa, O
Kurosawa, K
Ida, T
Harada, N
Kondoh, T
Miyake, N
Yoshiura, K
Kishino, T
Ohta, T
Niikawa, N
Matsumoto, N
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Human Genet, Nagasaki 8528523, Japan
[2] Kyushu Med Sci Nagasaki Lab, Nagasaki, Japan
[3] Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan
[4] Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki 852, Japan
[5] Japan Sci & Technol Corp, CREST, Kawaguchi, Japan
[6] Nagasaki Univ, Res Ctr Frontier Life Sci, Div Funct Genom, Nagasaki 852, Japan
关键词
inv dup del(8p); 8p23; inversion; polymorphism;
D O I
10.1002/ajmg.a.30063
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We analyzed five patients with inverted duplication deletion of 8p [inv dup del(8p)] using fluorescence in situ hybridization (FISH) and short tandem repeat polymorphism (STRP) analysis. In all patients, inv dup del(8p) consisted of a deleted distal segment, an intact in-between segment, and a duplicated proximal segment. In all of them, the proximal breakpoint of the deletion and one of the breakpoints of the duplication were identical, each located at one of the two olfactory receptor gene clusters at 8p23. FISH analysis showed all their mothers to be heterozygous carriers of an 8p23 inversion [inv(8)(p23)]. STRP analysis indicated that the deletions occurred in maternally derived chromosomes. The duplicated segments had two copies of maternal, either heterozygous or homozygous alleles. These findings support and reinforce those in 16 patients with inv dup del(8p) and their parents by Floridia et al. [1996: Am J Hum Genet 58:785-796] and subsequent additional studies of 10 of them by Giglio et al. [2001: Am J Hum Genet 68:874-883]. Based on these findings, we propose a model for the inv dup del(8p) formation. The inverted segment and its normal counterpart in inv(8)(p23) heterozygous carrier mothers form a loop at the pachytene period of meiosis I. Inv dup del(8p) with heterozygous duplication is formed through at least one meiotic recombination within the loop. Inv dup del(8p) with the homozygous duplication arises through two meiotic recombinations on the inv(8)(p23) chromosome (one within the loop and the other between the loop and centromere). Subsequent rescue by eliminating a part of the duplicated segment and a centromere enables formation of viable inv dup del(8p). The frequency of the inv(8)(p23) allele is 39% in a normal Japanese population, comparable to 26% in Europeans Giglio et al. [2001: Am J Hum Genet 68:874-883]. The proposed mechanism of formation of inv dup del(8p) requires two independent events (a recombination within the loop and subsequent rescue), which may explain its rarity. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:133 / 137
页数:5
相关论文
共 8 条
[1]   INVERSION DUPLICATION OF THE SHORT ARM OF CHROMOSOME-8 - CLINICAL-DATA ON 7 PATIENTS AND REVIEW OF THE LITERATURE [J].
DEDIESMULDERS, CEM ;
ENGELEN, JJM ;
SCHRANDERSTUMPEL, TRM ;
GOVAERTS, LCP ;
DEVRIES, B ;
VLES, JSH ;
WAGEMANS, A ;
SCHIJNSFLEUREN, S ;
GILLESSENKAESBACH, G ;
FRYNS, JP .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 59 (03) :369-374
[2]  
Floridia G, 1996, AM J HUM GENET, V58, P785
[3]   Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation [J].
Giglio, S ;
Calvari, V ;
Gregato, G ;
Gimelli, G ;
Camanini, S ;
Giorda, R ;
Ragusa, A ;
Guerneri, S ;
Selicorni, A ;
Stumm, M ;
Tonnies, H ;
Ventura, M ;
Zollino, M ;
Neri, G ;
Barber, J ;
Wieczorek, D ;
Rocchi, M ;
Zuffardi, O .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (02) :276-285
[4]   Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements [J].
Giglio, S ;
Broman, KW ;
Matsumoto, N ;
Calvari, V ;
Gimelli, G ;
Neumann, T ;
Ohashi, H ;
Voullaire, L ;
Larizza, D ;
Giorda, R ;
Weber, JL ;
Ledbetter, DH ;
Zuffardi, O .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (04) :874-883
[5]   CLINICAL AND CYTOGENETIC FINDINGS IN 7 CASES OF INVERTED DUPLICATION OF 8P WITH EVIDENCE OF A TELOMERIC DELETION USING FLUORESCENCE IN-SITU HYBRIDIZATION [J].
GUO, WJ ;
CALLIFDALEY, F ;
ZAPATA, MC ;
MILLER, ME .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (03) :230-236
[6]   An optimized set of human telomere clones for studying telomere integrity and architecture [J].
Knight, SJL ;
Lese, CM ;
Precht, KS ;
Kuc, J ;
Ning, Y ;
Lucas, S ;
Regan, R ;
Brenan, M ;
Nicod, A ;
Lawrie, NM ;
Cardy, DLN ;
Nguyen, H ;
Hudson, TJ ;
Riethman, HC ;
Ledbetter, DH ;
Flint, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) :320-332
[7]  
MADAN K, 1988, CYTOGENETICS MAMMALI, P249
[8]   Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23 [J].
Sugawara, H ;
Harada, N ;
Ida, T ;
Ishida, T ;
Ledbetter, DH ;
Yoshiura, KI ;
Ohta, T ;
Kishino, T ;
Niikawa, N ;
Matsumoto, N .
GENOMICS, 2003, 82 (02) :238-244