摘要: |
目的:(1) 建立Ⅰ型常染色体显性遗传多囊肾病(ADPKDⅠ)的基因诊断方法;(2) 寻找具有普遍意义的突变方式,以优化基因诊断。方法:(1) 采用Southern杂交和 PCR 方法, 调查ADPKDⅠ基因3′端单拷贝区突变情况;(2) PCR扩增分析微卫星SM7。结果:将AH4与16例患者的基因组DNA进行Southern杂交后, 均显示有正常的15 kb的杂交片段。对27例患者ADPKD Ⅰ基因3′端AH4和JH14两探针间的5.72 kb 基因组DNA行PCR扩增后,未发现5.5 kb基因组DNA缺失。109名正常人SM7 PCR扩增显示,其多态信息含量(PIC)值为0.76,3个家系的SM7 等位片段与疾病基因连锁关系明确。结论:在汉族中:(1) ADPKDⅠ基因3′ 端单拷贝区无常见性大片段基因组DNA缺失类突变;(2) SM7所含PIC 较高,用其可在70%?80%的ADPKDⅠ家系中作出基因诊断。 |
关键词: 肾,多囊,常染色体显性 突变 诊断,基因 |
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The gene diagnosis and mutation survey of autosomal dominant polycystic kidney diseaseⅠ |
焦炳华,陈建鹤,缪为民,齐隽,朱有华,闵志廉,王立明 |
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Abstract: |
Objective: To explore gene diagnosis of autosomal dominant polycystic kidney disease (ADPKDⅠ) and to look for the typical mutation to improve the gene diagnosis. Methods: Southern blot and PCR was used to observe the mutation condition of 3′end single copy region of ADPKDⅠ gene; Amplifing and analysing the microsatellite SM7 by PCR. Results: (1) After the probe AH4 was hybridized with 16 patients′ genomic DNA by Southern blot, the common 15 kb fragments were found in every one; (2) For 27 patients, 5.72 kb genomic DNA, which is between the probe AH4 and JH14, was amplified by PCR, and no 5. 5 kb genomic DNA deletion were found in this region; SM7 was amplified in 109 health persons, its PIC was 0.76, and was closely linked with ADPKD Ⅰ gene in 3 patients′ family. Conclusion:(1) No large genomic DNA segment deletion can be found frequently in ADPKD Ⅰ gene 3′end single copy region; (2) The PIC of SM7 is high, it can be used to make rapid gene diagnosis in about 70%?80%ADPKDⅠfamily. |
Key words: kidney, polycystic, autosomal dominant mutation diagnosis,gene |