Donnelly James G, Detombe Sarah, Hindmarsh J Thomas
Division of Biochemistry, The Ottawa Hospital, Ontario, Canada.
Ann Clin Lab Sci. 2002 Spring;32(2):107-13.
Single-strand conformational polymorphism and denaturing gel electrophoresis were used to screen for mutations in the protoporphyrinogen oxidase gene (PPOX) of three patients with clinically and biochemically proven variegate porphyria in order to select genomic regions for specific DNA sequence analysis. Two previously undescribed mutations were identified: PPOX1423-1426-delATCT and PPOX2272insG. Denaturing gel electrophoresis was able to discern the point mutation in exon 5 (PPOX2272insG) of the PPOX gene. Once an index individual has been identified, single-strand conformational polymorphism and denaturing gel electrophoresis techniques are useful to identify family members who may be unaffected carriers. Such identification can help potential cases to avoid medications and other triggers that could precipitate acute porphyric attacks.
采用单链构象多态性和变性凝胶电泳技术,对3例临床和生化检查确诊为杂合性卟啉病的患者的原卟啉原氧化酶基因(PPOX)进行突变筛查,以选择特定的基因组区域进行DNA序列分析。鉴定出两个此前未描述的突变:PPOX1423 - 1426 - delATCT和PPOX2272insG。变性凝胶电泳能够识别PPOX基因外显子5中的点突变(PPOX2272insG)。一旦确定了索引个体,单链构象多态性和变性凝胶电泳技术有助于识别可能为未受影响携带者的家庭成员。这种识别有助于潜在患者避免使用可能引发急性卟啉病发作的药物和其他诱因。