Literature DB >> 11231899

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.

S Giglio1, K W Broman, N Matsumoto, V Calvari, G Gimelli, T Neumann, H Ohashi, L Voullaire, D Larizza, R Giorda, J L Weber, D H Ledbetter, O Zuffardi.   

Abstract

The olfactory receptor (OR)-gene superfamily is the largest in the mammalian genome. Several of the human OR genes appear in clusters with > or = 10 members located on almost all human chromosomes, and some chromosomes contain more than one cluster. We demonstrate, by experimental and in silico data, that unequal crossovers between two OR gene clusters in 8p are responsible for the formation of three recurrent chromosome macrorearrangements and a submicroscopic inversion polymorphism. The first two macrorearrangements are the inverted duplication of 8p, inv dup(8p), which is associated with a distinct phenotype, and a supernumerary marker chromosome, +der(8)(8p23.1pter), which is also a recurrent rearrangement and is associated with minor anomalies. We demonstrate that it is the reciprocal of the inv dup(8p). The third macrorearrangment is a recurrent 8p23 interstitial deletion associated with heart defect. Since inv dup(8p)s originate consistently in maternal meiosis, we investigated the maternal chromosomes 8 in eight mothers of subjects with inv dup(8p) and in the mother of one subject with +der(8), by means of probes included between the two 8p-OR gene clusters. All the mothers were heterozygous for an 8p submicroscopic inversion that was delimited by the 8p-OR gene clusters and was present, in heterozygous state, in 26% of a population of European descent. Thus, inversion heterozygosity may cause susceptibility to unequal recombination, leading to the formation of the inv dup(8p) or to its reciprocal product, the +der(8p). After the Yp inversion polymorphism, which is the preferential background for the PRKX/PRKY translocation in XX males and XY females, the OR-8p inversion is the second genomic polymorphism that confers susceptibility to the formation of common chromosome rearrangements. Accordingly, it may be possible to develop a profile of the individual risk of having progeny with chromosome rearrangements.

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Year:  2001        PMID: 11231899      PMCID: PMC1275641          DOI: 10.1086/319506

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


  23 in total

Review 1.  Structure of chromosomal duplicons and their role in mediating human genomic disorders.

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Journal:  Genome Res       Date:  2000-05       Impact factor: 9.043

2.  Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

Authors:  H Kurahashi; T H Shaikh; E H Zackai; L Celle; D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  2000-07-20       Impact factor: 11.025

Review 3.  Many paths to the top of the mountain: diverse evolutionary solutions to centromere structure.

Authors:  C Tyler-Smith; G Floridia
Journal:  Cell       Date:  2000-07-07       Impact factor: 41.582

4.  Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

Authors:  S Giglio; S L Graw; G Gimelli; B Pirola; P Varone; L Voullaire; F Lerzo; E Rossi; C Dellavecchia; M C Bonaglia; M C Digilio; A Giannotti; B Marino; R Carrozzo; J R Korenberg; C Danesino; E Sujansky; B Dallapiccola; O Zuffardi
Journal:  Circulation       Date:  2000-07-25       Impact factor: 29.690

Review 5.  Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.

Authors:  W J Guo; F Callif-Daley; M C Zapata; M E Miller
Journal:  Am J Med Genet       Date:  1995-09-11

6.  Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis.

Authors:  S Saunier; J Calado; F Benessy; F Silbermann; R Heilig; J Weissenbach; C Antignac
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

7.  Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

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8.  A stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8p.

Authors:  H Ohashi; K Wakui; K Ogawa; T Okano; N Niikawa; Y Fukushima
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

Review 9.  Inverted duplication of 8p: ten new patients and review of the literature.

Authors:  G L Feldman; L Weiss; M C Phelan; R J Schroer; D L Van Dyke
Journal:  Am J Med Genet       Date:  1993-09-15

Review 10.  Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.

Authors:  C E de Die-Smulders; J J Engelen; C T Schrander-Stumpel; L C Govaerts; B de Vries; J S Vles; A Wagemans; S Schijns-Fleuren; G Gillessen-Kaesbach; J P Fryns
Journal:  Am J Med Genet       Date:  1995-11-20
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  108 in total

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Authors:  L R Osborne; M Li; B Pober; D Chitayat; J Bodurtha; A Mandel; T Costa; T Grebe; S Cox; L C Tsui; S W Scherer
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

2.  Complex evolution of 7E olfactory receptor genes in segmental duplications.

Authors:  Tera Newman; Barbara J Trask
Journal:  Genome Res       Date:  2003-05       Impact factor: 9.043

3.  Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster.

Authors:  E J Hollox; J A L Armour; J C K Barber
Journal:  Am J Hum Genet       Date:  2003-08-12       Impact factor: 11.025

4.  Evolution of olfactory receptor genes in the human genome.

Authors:  Yoshihito Niimura; Masatoshi Nei
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-24       Impact factor: 11.205

Review 5.  Chromosomal dynamics of human neocentromere formation.

Authors:  Peter E Warburton
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

Review 6.  The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.

Authors:  H Kurahashi; H Inagaki; T Ohye; H Kogo; M Tsutsumi; T Kato; M Tong; B S Emanuel
Journal:  Clin Genet       Date:  2010-10       Impact factor: 4.438

7.  Segmental duplications and copy-number variation in the human genome.

Authors:  Andrew J Sharp; Devin P Locke; Sean D McGrath; Ze Cheng; Jeffrey A Bailey; Rhea U Vallente; Lisa M Pertz; Royden A Clark; Stuart Schwartz; Rick Segraves; Vanessa V Oseroff; Donna G Albertson; Daniel Pinkel; Evan E Eichler
Journal:  Am J Hum Genet       Date:  2005-05-25       Impact factor: 11.025

8.  Accommodating chromosome inversions in linkage analysis.

Authors:  Gary K Chen; Erin Slaten; Roel A Ophoff; Kenneth Lange
Journal:  Am J Hum Genet       Date:  2006-06-06       Impact factor: 11.025

Review 9.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

10.  Segmental duplications flank the multiple sclerosis locus on chromosome 17q.

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Journal:  Genome Res       Date:  2004-07-15       Impact factor: 9.043

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