New variations of the EDNRB gene and its association with sporadic Hirschsprung's disease in Korea
The endothelin receptor B (EDNRB) signaling pathway, which is the second major susceptible gene for Hirschsprung's disease (HSCR), is crucial for the development of the enteric nervous system. The allele frequency of polymorphisms was mostly tested in the American and European population, but t...
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Published in | Journal of pediatric surgery Vol. 41; no. 10; pp. 1708 - 1712 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.10.2006
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Subjects | |
Online Access | Get full text |
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Summary: | The endothelin receptor B (EDNRB) signaling pathway, which is the second major susceptible gene for Hirschsprung's disease (HSCR), is crucial for the development of the enteric nervous system. The allele frequency of polymorphisms was mostly tested in the American and European population, but the data of an ethnically diverse, non-Caucasian population are unclear. To further investigate the variants and haplotypes of the
EDNRB gene, this study examined sequence variations in Korean patients with sporadic HSCR.
All 8 exons and intron/exon boundaries of the
EDNRB gene in 18 Korean patients with sporadic HSCR and 84 healthy individuals were screened using PCR amplification and direct sequencing.
A total of 8 different nucleotide substitutions were identified. Of these, 4 were new variants (promoter-116C>T; 5′UTR-121G>T; IVS4+62C>A; IVS5+121G>C) and the others were previously described variants. The distribution of variations was even different from that reported for Chinese and Japanese subjects as well as other ethnic groups. This study also analyzed the haplotypes for an association between the variants identified with HSCR.
This study identified additional sequence variants of the
EDNRB gene, but the estimated
EDNRB haplotypes did not show any disease risk. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-3468 1531-5037 |
DOI: | 10.1016/j.jpedsurg.2006.05.042 |