Literature DB >> 15726498

Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.

Gopalrao V N Velagaleti1, Gabriel A Bien-Willner, Jill K Northup, Lillian H Lockhart, Judy C Hawkins, Syed M Jalal, Marjorie Withers, James R Lupski, Pawel Stankiewicz.   

Abstract

Campomelic dysplasia (CD) is a semilethal skeletal malformation syndrome with or without XY sex reversal. In addition to the multiple mutations found within the sex-determining region Y-related high-mobility group box gene (SOX9) on 17q24.3, several chromosome anomalies (translocations, inversions, and deletions) with breakpoints scattered over 1 Mb upstream of SOX9 have been described. Here, we present a balanced translocation, t(4;17)(q28.3;q24.3), segregating in a family with a mild acampomelic CD with Robin sequence. Both chromosome breakpoints have been identified by fluorescence in situ hybridization and have been sequenced using a somatic cell hybrid. The 17q24.3 breakpoint maps approximately 900 kb upstream of SOX9, which is within the same bacterial artificial chromosome clone as the breakpoints of two other reported patients with mild CD. We also report a prenatal identification of acampomelic CD with male-to-female sex reversal in a fetus with a de novo balanced complex karyotype, 46,XY,t(4;7;8;17)(4qter-->4p15.1::17q25.1-->17qter;7qter-->7p15.3::4p15.1-->4pter;8pter-->8q12.1::7p15.3-->7pter;17pter-->17q25.1::8q12.1-->8qter). Surprisingly, the 17q breakpoint maps approximately 1.3 Mb downstream of SOX9, making this the longest-range position effect found in the field of human genetics and the first report of a patient with CD with the chromosome breakpoint mapping 3' of SOX9. By using the Regulatory Potential score in conjunction with analysis of the rearrangement breakpoints, we identified a candidate upstream cis-regulatory element, SOX9cre1. We provide evidence that this 1.1-kb evolutionarily conserved element and the downstream breakpoint region colocalize with SOX9 in the interphase nucleus, despite being located 1.1 Mb upstream and 1.3 Mb downstream of it, respectively. The potential molecular mechanism responsible for the position effect is discussed.

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Year:  2005        PMID: 15726498      PMCID: PMC1199302          DOI: 10.1086/429252

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


  51 in total

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2.  Variable expression of rib, pectus, and scapular anomalies with Robin-type cleft palate in a 5-generation family: a new syndrome?

Authors:  H J Stalker; R T Zori
Journal:  Am J Med Genet       Date:  1997-12-19

3.  Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4.

Authors:  Y J de Kok; E R Vossenaar; C W Cremers; N Dahl; J Laporte; L J Hu; D Lacombe; N Fischel-Ghodsian; R A Friedman; L S Parnes; P Thorpe; M Bitner-Glindzicz; H J Pander; H Heilbronner; J Graveline; J T den Dunnen; H G Brunner; H H Ropers; F P Cremers
Journal:  Hum Mol Genet       Date:  1996-09       Impact factor: 6.150

4.  A novel germ line mutation in SOX9 causes familial campomelic dysplasia and sex reversal.

Authors:  F J Cameron; R M Hageman; C Cooke-Yarborough; C Kwok; L L Goodwin; D O Sillence; A H Sinclair
Journal:  Hum Mol Genet       Date:  1996-10       Impact factor: 6.150

5.  Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations.

Authors:  J Meyer; P Südbeck; M Held; T Wagner; M L Schmitz; F D Bricarelli; E Eggermont; U Friedrich; O A Haas; A Kobelt; J G Leroy; L Van Maldergem; E Michel; B Mitulla; R A Pfeiffer; A Schinzel; H Schmidt; G Scherer
Journal:  Hum Mol Genet       Date:  1997-01       Impact factor: 6.150

6.  Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene.

Authors:  J W Foster; M A Dominguez-Steglich; S Guioli; C Kwok; P A Weller; M Stevanović; J Weissenbach; S Mansour; I D Young; P N Goodfellow
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8.  A clinical and genetic study of campomelic dysplasia.

Authors:  S Mansour; C M Hall; M E Pembrey; I D Young
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

9.  A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred.

Authors:  C J Williams; A Ganguly; E Considine; S McCarron; D J Prockop; C Walsh-Vockley; V V Michels
Journal:  Am J Med Genet       Date:  1996-06-14

10.  Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.

Authors:  C Kwok; P A Weller; S Guioli; J W Foster; S Mansour; O Zuffardi; H H Punnett; M A Dominguez-Steglich; J D Brook; I D Young
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

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  60 in total

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5.  Computational Prediction of Position Effects of Human Chromosome Rearrangements.

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Journal:  Curr Protoc Hum Genet       Date:  2018-04-26

6.  Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.

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7.  A misplaced lncRNA causes brachydactyly in humans.

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9.  A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E.

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10.  Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.

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