摘要
报道在dystrophin基因内新发现四个TaqⅠ限制性片段长度多态,用dystrophincDNA1—2a检测到的TaqⅠ等位片段是4.0kb(A1)和3.3kb(A2),用CDNA2b—3检测到的TaqⅠ等位片段是7.2kb(A1)和6.8kb(A2)。用cDNA5b—7检测到两对新的TaqⅠ等位片段,分别是10.0kb(A1)和8.4kb(A2),以及2.55kb(C1)和1.6kb(C2)片段。在45个DMD/BMD家系的基因检测中,这四对新的等位片段,在部分家系的上下代传递中分别呈孟德尔遗传学分离。它们的实际观察杂合体频率依次是:0.29,0.07,0.04和0.18,预期杂合体频率是0.20,0.06,0.02和0.20。这些新的TaqⅠ限制性片段长度多态,已在杜氏肌营养不良症家系的遗传连锁分析及致病基因携带者的诊断中,显示出较高的;临床应用价值。
Four new Taq Ⅰ polymorphisms in dystrophin gene are reported here. A pair of allele fragment (4. 0 kb and 3. 3 kb) were detected by cDNA1- 2a,another pair (7. 2 kb and 6. 8 kb) by cDNA 2b - 3,and the other two pairs (10. 0kb and 8. 4kb, 2. 55kb and 1. 6kb) by cDNA 5b-7. The observed heterozygote frequencies (OHF) of the Four RFLPs were 0. 29,0. 07,0. 04 and 0. 18 respectively and the expected heterozygote frequencies (EHF) of them were 0. 20,0. 06,0. 02 and 0. 20. They had been tested in linkage analysis of DMD families and had shown a high utility in clinics.
出处
《复旦学报(自然科学版)》
CSCD
北大核心
1995年第4期379-384,共6页
Journal of Fudan University:Natural Science