Department of Pediatric Surgery, Major Laboratory of Chinese Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University, 36 Sanhao Street Heping District, Shenyang, 110004, PR China.
Department of Pediatric Surgery, Major Laboratory of Chinese Health Ministry for Congenital Malformations, Shengjing Hospital of China Medical University, 36 Sanhao Street Heping District, Shenyang, 110004, PR China.
Exp Mol Pathol. 2014 Apr;96(2):219-24. doi: 10.1016/j.yexmp.2014.02.004. Epub 2014 Feb 24.
Hirschsprung's disease (HSCR) is the third most common congenital disorder of the gastrointestinal tract. It is an anomalous enteric nervous system (ENS) characterized by the absence of ganglion cells in the myenteric and submucosal plexuses. It has been reported that the Smad-interacting protein 1(SIP1) is critical in embryonic development of ENS for its regulation on neural crest cells. In the present study, we analyzed 3 polymorphisms of the SIP1 gene rs41292293 (exon5), rs34961586 (exon6) and rs13017697 (exon8) to determine their potential contributions to the susceptibility of HSCR. Allele frequencies and genotype distributions were analyzed by sequence analysis in 107 HSCR patients and 107 normal controls. The SIP1 expression was carried out by using real-time PCR, western blot and immunohistochemistry. Polymorphic analysis indicated that the genotype distributions and allele frequencies in SIP1 gene rs41292293, rs34961586 and rs13017697 were statistically different between HSCR and normal controls. The expression analysis revealed that SIP1 was ectopically expressed in the aganglionic segments; neither the mRNA nor the protein levels demonstrated that the difference compared with those was in the normal segments. In conclusion, the single nucleotide polymorphisms in SIP1 gene rs41292293, rs34961586 and rs13017697 are associated with the ectopic expression of this gene in human HSCR and contribute to the susceptibility of this disease in population.
先天性巨结肠症(HSCR)是胃肠道最常见的三种先天性疾病之一。它是一种异常的肠神经系统(ENS),其特征是在肌间和黏膜下神经丛中缺乏神经节细胞。据报道,Smad 相互作用蛋白 1(SIP1)在 ENS 的胚胎发育中起着关键作用,因为它可以调节神经嵴细胞。在本研究中,我们分析了 SIP1 基因的 3 个多态性 rs41292293(外显子 5)、rs34961586(外显子 6)和 rs13017697(外显子 8),以确定它们对 HSCR 易感性的潜在贡献。通过序列分析在 107 例 HSCR 患者和 107 例正常对照中分析了等位基因频率和基因型分布。通过实时 PCR、western blot 和免疫组织化学分析了 SIP1 的表达。多态性分析表明,SIP1 基因 rs41292293、rs34961586 和 rs13017697 的基因型分布和等位基因频率在 HSCR 和正常对照组之间存在统计学差异。表达分析表明,SIP1 在无神经节的节段中异位表达;与正常节段相比,mRNA 和蛋白质水平均未显示出差异。总之,SIP1 基因 rs41292293、rs34961586 和 rs13017697 的单核苷酸多态性与该基因在人类 HSCR 中的异位表达有关,并导致该疾病在人群中的易感性。