Literature DB >> 11115062

Genetic evidence for a novel gene(s) involved in urogenital development on 10q26.

T Ogata1, K Muroya, I Sasagawa, T Kosho, K Wakui, S Sakazume, K Ito, N Matsuo, H Ohashi, T Nagai.   

Abstract

BACKGROUND: Although the frequent association between distal 10q monosomy and urogenital anomalies suggests the presence of a gene(s) for urogenital development on distal 10q, molecular deletion mapping has not been performed for the putative gene(s). In this study, we examined genotype-phenotype correlations in patients with distal 10q monosomy.
METHODS: This study consisted of six karyotypic males (cases 1 through 6) and four karyotypic females (cases 7 through 10) with 10q26 monosomy. Cases 3 through 5 and 7 through 10 had urinary anomalies such as vesicoureteral reflux and hypoplastic kidney, and cases 1 through 6, 8, and 9 exhibited genital anomalies such as micropenis, hypospadias, cryptorchidism, and hypoplastic labia majora. Fluorescence in situ hybridization (FISH) for 10q telomere, whole chromosome 10 painting, and microsatellite analysis for 35 loci on distal 10q were performed in cases 1 through 8.
RESULTS: FISH and whole chromosome painting confirmed distal 10q monosomy in cases 1 through 8. Microsatellite analysis revealed that hemizygosity for the region distal to D10S186 was shared by cases with urinary anomalies and that for the region distal to D10S1248 was common to cases with genital anomalies. Furthermore, it was indicated that PAX2, GFRA1, and EMX2 on distal 10q, in which the deletions could affect urinary and/or genital development, were present in two copies in cases 1 through 8.
CONCLUSIONS: The results suggest that a novel gene(s) for urinary development and that for genital development reside in the approximately 20 cM region distal to D10S186 and in the approximately 10 cM region distal to D10S1248, respectively, although it remains to be determined whether the two types of genes are identical or different.

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Year:  2000        PMID: 11115062     DOI: 10.1046/j.1523-1755.2000.00412.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  20 in total

1.  A genome-wide scan for genes involved in primary vesicoureteric reflux.

Authors:  H Kelly; C M Molony; J M Darlow; M E Pirker; A Yoneda; A J Green; P Puri; D E Barton
Journal:  J Med Genet       Date:  2007-07-27       Impact factor: 6.318

2.  Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.

Authors:  Nathaniel D Miller; Melonie A Nance; Elizabeth S Wohler; Julie E Hoover-Fong; Emily Lisi; George H Thomas; Jonathan Pevsner
Journal:  Am J Med Genet A       Date:  2009-02-15       Impact factor: 2.802

Review 3.  Genetics of vesicoureteral reflux.

Authors:  Prem Puri; Jan-Hendrik Gosemann; John Darlow; David E Barton
Journal:  Nat Rev Urol       Date:  2011-08-23       Impact factor: 14.432

4.  Prevalence of genetic renal disease in children.

Authors:  Jeffery Fletcher; Stephen McDonald; Stephen I Alexander
Journal:  Pediatr Nephrol       Date:  2012-09-29       Impact factor: 3.714

Review 5.  Renal hypoplasia: lessons from Pax2.

Authors:  Alison Dziarmaga; Jacklyn Quinlan; Paul Goodyer
Journal:  Pediatr Nephrol       Date:  2005-11-05       Impact factor: 3.714

Review 6.  Genetic basis of human congenital anomalies of the kidney and urinary tract.

Authors:  Simone Sanna-Cherchi; Rik Westland; Gian Marco Ghiggeri; Ali G Gharavi
Journal:  J Clin Invest       Date:  2018-01-02       Impact factor: 14.808

7.  Mechanisms of ring chromosome formation, ring instability and clinical consequences.

Authors:  Roberta S Guilherme; Vera F Ayres Meloni; Chong A Kim; Renata Pellegrino; Sylvia S Takeno; Nancy B Spinner; Laura K Conlin; Denise M Christofolini; Leslie D Kulikowski; Maria I Melaragno
Journal:  BMC Med Genet       Date:  2011-12-21       Impact factor: 2.103

8.  Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24.

Authors:  Shazia Ashraf; Bethan E Hoskins; Hassan Chaib; Julia Hoefele; Andreas Pasch; Pawaree Saisawat; Friedrich Trefz; Hans W Hacker; Gudrun Nuernberg; Peter Nuernberg; Edgar A Otto; Friedhelm Hildebrandt
Journal:  Nephrol Dial Transplant       Date:  2009-12-10       Impact factor: 5.992

Review 9.  Ring chromosome 10: report on two patients and review of the literature.

Authors:  Roberta Santos Guilherme; Chong Ae Kim; Luis Garcia Alonso; Rachel S Honjo; Vera Ayres Meloni; Denise Maria Christofolini; Leslie Domenici Kulikowski; Maria Isabel Melaragno
Journal:  J Appl Genet       Date:  2012-12-18       Impact factor: 3.240

10.  Global survey of protein expression during gonadal sex determination in mice.

Authors:  Katherine Ewen; Mark Baker; Dagmar Wilhelm; R John Aitken; Peter Koopman
Journal:  Mol Cell Proteomics       Date:  2009-07-17       Impact factor: 5.911

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