Literature DB >> 15580547

Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion.

Remco Visser1, Osamu Shimokawa, Naoki Harada, Akira Kinoshita, Tohru Ohta, Norio Niikawa, Naomichi Matsumoto.   

Abstract

Sotos syndrome (SoS) is a congenital dysmorphic disorder characterized by overgrowth in childhood, distinctive craniofacial features, and mental retardation. Haploinsufficiency of the NSD1 gene owing to either intragenic mutations or microdeletions is known to be the major cause of SoS. The common approximately 2.2-Mb microdeletion encompasses the whole NSD1 gene and neighboring genes and is flanked by low-copy repeats (LCRs). Here, we report the identification of a 3.0-kb major recombination hotspot within these LCRs, in which we mapped deletion breakpoints in 78.7% (37/47) of patients with SoS who carry the common microdeletion. The deletion size was subsequently refined to 1.9 Mb. Sequencing of breakpoint fragments from all 37 patients revealed junctions between a segment of the proximal LCR (PLCR-B) and the corresponding region of the distal LCR (DLCR-2B). PLCR-B and DLCR-2B are the only directly oriented regions, whereas the remaining regions of the PLCR and DLCR are in inverted orientation. The PLCR, with a size of 394.0 kb, and the DLCR, with a size of of 429.8 kb, showed high overall homology (approximately 98.5%), with an increased sequence similarity (approximately 99.4%) within the 3.0-kb breakpoint cluster. Several recombination-associated motifs were identified in the hotspot and/or its vicinity. Interestingly, a 10-fold average increase of a translin motif, as compared with the normal distribution within the LCRs, was recognized. Furthermore, a heterozygous inversion of the interval between the LCRs was detected in all fathers of the children carrying a deletion in the paternally derived chromosome. The functional significance of these findings remains to be elucidated. Segmental duplications of the primate genome play a major role in chromosomal evolution. Evolutionary study showed that the duplication of the SoS LCRs occurred 23.3-47.6 million years ago, before the divergence of Old World monkeys.

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Year:  2004        PMID: 15580547      PMCID: PMC1196433          DOI: 10.1086/426950

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  46 in total

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2.  Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

Authors:  Weimin Bi; Sung-Sup Park; Christine J Shaw; Marjorie A Withers; Pragna I Patel; James R Lupski
Journal:  Am J Hum Genet       Date:  2003-11-24       Impact factor: 11.025

3.  Genotype-phenotype correlation in patients suspected of having Sotos syndrome.

Authors:  Lonneke de Boer; Sarina G Kant; Marcel Karperien; Lotte van Beers; Jennifer Tjon; Geraldine R Vink; Dewy van Tol; Hans Dauwerse; Saskia le Cessie; Frits A Beemer; Ineke van der Burgt; Ben C J Hamel; Raoul C Hennekam; Ursula Kuhnle; Inge B Mathijssen; Hermine E Veenstra-Knol; Connie T Schrander Stumpel; Martijn H Breuning; Jan M Wit
Journal:  Horm Res       Date:  2004-09-24

4.  Sotos syndrome: a study of the diagnostic criteria and natural history.

Authors:  T R Cole; H E Hughes
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

5.  Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot.

Authors:  H Kiyosawa; P F Chance
Journal:  Hum Mol Genet       Date:  1996-06       Impact factor: 6.150

6.  The translin ring specifically recognizes DNA ends at recombination hot spots in the human genome.

Authors:  M Kasai; T Matsuzaki; K Katayanagi; A Omori; R T Maziarz; J L Strominger; K Aoki; K Suzuki
Journal:  J Biol Chem       Date:  1997-04-25       Impact factor: 5.157

7.  Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substrates.

Authors:  Christine J Shaw; Marjorie A Withers; James R Lupski
Journal:  Am J Hum Genet       Date:  2004-05-13       Impact factor: 11.025

8.  A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

Authors:  L T Reiter; T Murakami; T Koeuth; L Pentao; D M Muzny; R A Gibbs; J R Lupski
Journal:  Nat Genet       Date:  1996-03       Impact factor: 38.330

9.  Genetics of Sotos syndrome.

Authors:  Remco Visser; Naomichi Matsumoto
Journal:  Curr Opin Pediatr       Date:  2003-12       Impact factor: 2.856

10.  Molecular characterization of inv dup del(8p): analysis of five cases.

Authors:  Osamu Shimokawa; Kenji Kurosawa; Tomoko Ida; Naoki Harada; Tatsuro Kondoh; Noriko Miyake; Kohichiro Yoshiura; Tatsuya Kishino; Tohru Ohta; Norio Niikawa; Naomichi Matsumoto
Journal:  Am J Med Genet A       Date:  2004-07-15       Impact factor: 2.802

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  33 in total

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2.  Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction.

Authors:  Christelle Borel; Fanny Cheung; Helen Stewart; David A Koolen; Christopher Phillips; N Simon Thomas; Patricia A Jacobs; Stephan Eliez; Andrew J Sharp
Journal:  Hum Genet       Date:  2012-05-30       Impact factor: 4.132

3.  Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis.

Authors:  Xingyi Guo; Maria Delio; Nousin Haque; Raquel Castellanos; Matthew S Hestand; Joris R Vermeesch; Bernice E Morrow; Deyou Zheng
Journal:  Hum Mol Genet       Date:  2016-07-19       Impact factor: 6.150

4.  Pronounced maternal parent-of-origin bias for type-1 NF1 microdeletions.

Authors:  Lisa Neuhäusler; Anna Summerer; David N Cooper; Victor-F Mautner; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2018-05-05       Impact factor: 4.132

5.  Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture.

Authors:  R Ciccone; T Mattina; R Giorda; M C Bonaglia; M Rocchi; T Pramparo; O Zuffardi
Journal:  J Med Genet       Date:  2006-05       Impact factor: 6.318

6.  Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.

Authors:  Marzena Gajecka; Adam Pavlicek; Caron D Glotzbach; Blake C Ballif; Malgorzata Jarmuz; Jerzy Jurka; Lisa G Shaffer
Journal:  Hum Genet       Date:  2006-07-18       Impact factor: 4.132

Review 7.  From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.

Authors:  Beverly S Emanuel; Sulagna C Saitta
Journal:  Nat Rev Genet       Date:  2007-11       Impact factor: 53.242

8.  Polymorphic micro-inversions contribute to the genomic variability of humans and chimpanzees.

Authors:  Justyna M Szamalek; David N Cooper; Werner Schempp; Peter Minich; Matthias Kohn; Josef Hoegel; Violaine Goidts; Horst Hameister; Hildegard Kehrer-Sawatzki
Journal:  Hum Genet       Date:  2005-12-16       Impact factor: 4.132

9.  Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination.

Authors:  Joke Vandewalle; Hilde Van Esch; Karen Govaerts; Jelle Verbeeck; Christiane Zweier; Irene Madrigal; Montserrat Mila; Elly Pijkels; Isabel Fernandez; Jürgen Kohlhase; Christiane Spaich; Anita Rauch; Jean-Pierre Fryns; Peter Marynen; Guy Froyen
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

Review 10.  On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.

Authors:  David N Cooper; Albino Bacolla; Claude Férec; Karen M Vasquez; Hildegard Kehrer-Sawatzki; Jian-Min Chen
Journal:  Hum Mutat       Date:  2011-09-02       Impact factor: 4.878

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