Comparison of FISH, PRINS, and conventional and fluorescent PCR for single-cell sexing, suitability for preimplantation genetic diagnosis

被引:12
作者
Findlay, I [1 ]
Corby, N [1 ]
Rutherford, A [1 ]
Quirke, P [1 ]
机构
[1] Univ Leeds, Ctr Reprod Growth & Dev, Inst Pathol, Leeds, W Yorkshire, England
关键词
flourescent in situ hybridization; single-cell PCR; preimplantation genetic diagnosis; primed in situ synthesis; sexing;
D O I
10.1023/A:1022584225311
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Although conventional polymerase chain reaction (PCR) was the first method used for sexing in preimplantation genetic diagnosis, fluorescent in situ hybridization (FISH) has become the method of choice. Recently two new techniques, primed in situ synthesis (PRINS) and fluorescent PCR, have been developed. This study compares the reliability and accuracy of these four techniques in single cells. Results: In buccal cells, fluorescent PCR and FISH had similar reliability (94 and 93%) and accuracy (97 and 96%) rates. The reliability and accuracy of PRINS (91 and 25%) and conventional PCR (79 and 89%) were lower. In human blastomeres, FISH and flourescent PCR had similar reliability (100%, 7/7; 95%, 190/201) rates. Accuracy rates,cere 71 % (5/7) and 99% (188/190)for FISH and fluorescent PCR, respecticely, however; too few blastomeres were analyzed by FISH for meaningful comparison. However; when these data are compared,with published data, the method of choice for blastomere sexing appears to be fluorescent PCR. Conclusions: Flouroscent PCR has major implications for PGD.
引用
收藏
页码:258 / 265
页数:8
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