Literature DB >> 12837273

Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23.

Hirobumi Sugawara1, Naoki Harada, Tomoko Ida, Takafumi Ishida, David H Ledbetter, Ko-ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Norio Niikawa, Naomichi Matsumoto.   

Abstract

To characterize a submicroscopic, common 8p23 polymorphic inversion, we constructed a complete BAC/PAC-based physical map covering the entire 4.7-Mb inversion and its flanking regions. Two low-copy repeats (LCRs), REPD (approximately 1.3 Mb) and REPP (approximately 0.4 Mb), were identified at each of the inversion breakpoints. Comparison of the REPD and REPP sequences revealed that REPD showed high homology to REPP, with complex direct and inverted orientations. REPD and REPP contain six and five olfactory receptor gene-related sequences, respectively. LCRs at 8p23 showed multiple FISH signals from an Old World monkey to the human. Thus, multiplication of the LCR may have occurred at least 21-25 million years ago. We also investigated the frequency of the 4.7-Mb inversion in the general Japanese population and found that the allele frequency for the 8p23 inversion was estimated to be 27%.

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Year:  2003        PMID: 12837273     DOI: 10.1016/s0888-7543(03)00108-3

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  30 in total

Review 1.  Chromosomal dynamics of human neocentromere formation.

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

2.  Evidence for large inversion polymorphisms in the human genome from HapMap data.

Authors:  Vikas Bansal; Ali Bashir; Vineet Bafna
Journal:  Genome Res       Date:  2006-12-21       Impact factor: 9.043

3.  A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects.

Authors:  Fei Long; Xike Wang; Shaohai Fang; Yuejuan Xu; Kun Sun; Sun Chen; Rang Xu
Journal:  PLoS One       Date:  2013-08-29       Impact factor: 3.240

4.  Large-scale recombination rate patterns are conserved among human populations.

Authors:  David Serre; Robert Nadon; Thomas J Hudson
Journal:  Genome Res       Date:  2005-11       Impact factor: 9.043

5.  Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype.

Authors:  A Wischmeijer; P Magini; R Giorda; M Gnoli; R Ciccone; L Cecconi; E Franzoni; L Mazzanti; G Romeo; O Zuffardi; M Seri
Journal:  Mol Syndromol       Date:  2010-11-25

Review 6.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

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

7.  Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

Authors:  Hela Ben Khelifa; Molka Kammoun; Hanene Hannachi; Najla Soyah; Saber Hammami; Hatem Elghezal; Damien Sanlaville; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Pediatr Genet       Date:  2015-10-14

8.  Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins.

Authors:  Suhaili Abu Bakar; Edward J Hollox; John A L Armour
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-08       Impact factor: 11.205

9.  Nucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphism.

Authors:  Nina Bosch; Marta Morell; Immaculada Ponsa; Josep Maria Mercader; Lluís Armengol; Xavier Estivill
Journal:  PLoS One       Date:  2009-12-14       Impact factor: 3.240

10.  Characterization of six human disease-associated inversion polymorphisms.

Authors:  Francesca Antonacci; Jeffrey M Kidd; Tomas Marques-Bonet; Mario Ventura; Priscillia Siswara; Zhaoshi Jiang; Evan E Eichler
Journal:  Hum Mol Genet       Date:  2009-04-21       Impact factor: 6.150

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