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Methylation analysis of EDNRB in human colon tissues of Hirschsprung’s disease
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  • 作者:Weibing Tang (1) (3)
    Bo Li (1) (3)
    Junwei Tang (1) (3)
    Kang Liu (1) (3)
    Jingjing Qin (1) (3)
    Wei Wu (1) (2)
    Qiming Geng (3)
    Jie Zhang (3)
    Huan Chen (3)
    Xiaoqun Xu (1) (3)
    Yankai Xia (1) (2)
  • 关键词:EDNRB ; Hirschsprung’s disease ; Methylation ; miRNA
  • 刊名:Pediatric Surgery International
  • 出版年:2013
  • 出版时间:July 2013
  • 年:2013
  • 卷:29
  • 期:7
  • 页码:683-688
  • 全文大小:234KB
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    9. Fernández RM, Sánchez-Mejías A, Mena MD, Ruiz-Ferrer M, López-Alonso M, Anti?olo G, Borrego S (2009) A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung disease. Ann Hum Genet 73(1):19-5. doi:10.1111/j.1469-1809.2008.00479.x CrossRef
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  • 作者单位:Weibing Tang (1) (3)
    Bo Li (1) (3)
    Junwei Tang (1) (3)
    Kang Liu (1) (3)
    Jingjing Qin (1) (3)
    Wei Wu (1) (2)
    Qiming Geng (3)
    Jie Zhang (3)
    Huan Chen (3)
    Xiaoqun Xu (1) (3)
    Yankai Xia (1) (2)

    1. State Key Laboratory of Reproductive Medicine, Institute of Toxicology, School of Public Health, Nanjing Medical University, Nanjing, 210029, China
    3. Department of Pediatric Surgery, Nanjing Children’s Hospital Affiliated Nanjing Medical University, Nanjing, 210008, China
    2. Key Laboratory of Modern Toxicology, Nanjing Medical University, Ministry of Education, Nanjing, China
  • ISSN:1437-9813
文摘
Purpose Hirschsprung’s disease (HSCR) is characterized by absence of the enteric nervous system in a variable portion of the distal gut. The endothelin receptor type B (EDNRB) gene has been localized to the chromosome 13q22 region and encodes a G-protein coupled receptor, is generally accepted as a crucial gene for HSCR. This study is to identify the epigenetic changes of EDNRB in the pathogenesis of HSCR. Methods We investigated the expression levels of EDNRB in 58 HSCR patients and 25 unrelated controls, using reverse transcriptase polymerase chain reaction (RT-PCR) and western blot assay. Moreover, using the methylation-specific polymerase chain reaction, we examined the methylation status of the promoter region of EDNRB. Results Aberrant high expression level of EDNRB was detected in HSCR patients compared with the control group (P?=?0.023). Besides, western blot assay confirmed the up-regulation of EDNRB in the post transcription level in the aganglionosis segment of HSCR patients. Furthermore, there was a significantly lower ratio of methylation level of EDNRB in HSCR. Conclusions Our study demonstrates that epigenetic inactivation of the EDNRB gene may play a role in the development of HSCR.

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