Hellani Ali, Coskun Serdar, Benkhalifa Moncef, Tbakhi Abelghani, Sakati Nadia, Al-Odaib Ali, Ozand Pinar
King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Mol Hum Reprod. 2004 Nov;10(11):847-52. doi: 10.1093/molehr/gah114. Epub 2004 Oct 1.
Multiple displacement amplification (MDA) is a technique used in the amplification of very low amounts of DNA and reported to yield large quantities of high-quality DNA. We used MDA to amplify the whole genome directly from a single cell. The most common techniques used in PGD are PCR and fluorescent in-situ hybridization (FISH). There are many limitations to these techniques including, the number of chromosomes diagnosed for FISH or the quality of DNA issued from a single cell PCR. This report shows, for the first time, use of MDA for single cell whole genome amplification. A total of 16 short tandem repeats (STRs) were amplified successfully with a similar pattern to the genomic DNA. Furthermore, allelic drop out (ADO) derived from MDA was assessed in 40 single cells by analysing (i) heterozygosity for a known beta globin mutation (IVSI-5 C-G) and by studying (ii) the heterozygous loci present in the STRs. ADO turned out to be 10.25% for the beta globin gene sequencing and 5% for the fluorescent PCR analysis of STRs. Moreover, the amplification accuracy of MDA permitted the detection of trisomy 21 on a single cell using comparative genome hybridization-array. Altogether, these data suggest that MDA can be used for single cell molecular karyotyping and the diagnosis of any single gene disorder in PGD.
多重置换扩增(MDA)是一种用于扩增极少量DNA的技术,据报道可产生大量高质量的DNA。我们使用MDA直接从单个细胞中扩增全基因组。植入前基因诊断(PGD)中最常用的技术是聚合酶链反应(PCR)和荧光原位杂交(FISH)。这些技术存在许多局限性,包括FISH诊断的染色体数量或单细胞PCR产生的DNA质量。本报告首次展示了使用MDA进行单细胞全基因组扩增。共成功扩增了16个短串联重复序列(STR),其模式与基因组DNA相似。此外,通过分析(i)已知β珠蛋白突变(IVSI-5 C-G)的杂合性以及研究(ii)STR中存在的杂合位点,对40个单细胞中源自MDA的等位基因脱失(ADO)进行了评估。β珠蛋白基因测序的ADO为10.25%,STR荧光PCR分析的ADO为5%。此外,MDA的扩增准确性使得能够使用比较基因组杂交阵列在单个细胞上检测21三体。总之,这些数据表明MDA可用于单细胞分子核型分析以及PGD中任何单基因疾病的诊断。