Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?

被引:8
作者
De Gregori, M
Pramparo, T
Memo, L
Gimelli, G
Messa, J
Rocchi, M
Patricelli, M
Ciccone, R
Giorda, R
Zuffardi, O
机构
[1] Univ Pavia, I-27100 Pavia, Italy
[2] UOC Patol Neonatal, Amb Genet CLin, Treviso, Italy
[3] Citogenet Osped G Gaslini, Genoa, Italy
[4] DAPEG Sez Genet, Bari, Italy
[5] IRCCS La Nostra Famiglia, Lecce, Italy
[6] Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
关键词
12p duplication; low copy repeats; segmental duplications; recurrent rearrangements; PipMaker analysis;
D O I
10.1007/s00439-005-0008-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe the characterization of an interstitial duplication of 12p, dup(12)(p11.21p13.31), by array-CGH and FISH in a patient with mental retardation and dysmorphic features. The sequence analysis of the breakpoints revealed the presence of homologous low copy repeats (LCRs) flanking the duplication region, thus suggesting that they have mediated the rearrangement. Pip-maker analysis showed that a third cluster of homologous LCRs lie distally to the two mediating the 12p duplication. We hypothesize that this duplication might be a new recurrent rearrangement and that, thanks to the different orientations of the homologous regions lying within each cluster, the three clusters are responsible for at least some of the several 12p aneuploidies reported in the literature such as direct and inverted duplications, deletions and supernumerary analphoid chromosomes. Moreover, we excluded that polymorphic inversions between these three clusters are present in the normal population.
引用
收藏
页码:207 / 213
页数:7
相关论文
共 33 条
[1]  
Allen TL, 1996, AM J MED GENET, V63, P250, DOI 10.1002/(SICI)1096-8628(19960503)63:1<250::AID-AJMG43>3.0.CO
[2]  
2-K
[3]   Localization of Chl1-related helicase genes to human chromosome regions 12p11 and 12p13: Similarity between parts of these genes and conserved human telomeric-associated DNA [J].
Amann, J ;
Valentine, W ;
Kidd, VJ ;
Lahti, JM .
GENOMICS, 1996, 32 (02) :260-265
[4]   Neocentromeres: Role in human disease, evolution, and centromere study [J].
Amor, DJ ;
Choo, KHA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) :695-714
[5]   The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats [J].
Barbouti, A ;
Stankiewicz, P ;
Nusbaum, C ;
Cuomo, C ;
Cook, A ;
Höglund, M ;
Johansson, B ;
Hagemeijer, A ;
Park, SS ;
Mitelman, F ;
Lupski, JR ;
Fioretos, T .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (01) :1-10
[6]   Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome:: extraordinary finding of an analphoid, inverted duplicated marker [J].
Dufke, A ;
Walczak, C ;
Liehr, T ;
Starke, H ;
Trifonov, V ;
Rubtsov, N ;
Schöning, M ;
Enders, H ;
Eggermann, T .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (08) :572-576
[7]   Structural dynamics of eukaryotic chromosome evolution [J].
Eichler, EE ;
Sankoff, D .
SCIENCE, 2003, 301 (5634) :793-797
[8]   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
[9]   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
[10]   Molecular structure and evolution of an alpha satellite non-alpha satellite junction at 16p11 [J].
Horvath, JE ;
Viggiano, L ;
Loftus, BJ ;
Adams, MD ;
Archidiacono, N ;
Rocchi, M ;
Eichler, EE .
HUMAN MOLECULAR GENETICS, 2000, 9 (01) :113-123