Pellestor F, Girardet A, Andréo B, Lefort G, Charlieu J P
Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Fertil Steril. 1996 Nov;66(5):781-6. doi: 10.1016/s0015-0282(16)58636-1.
To present the use of primed in situ labeling method in preimplantation diagnosis.
Double- and triple-primed in situ labeling were performed on 10 morphologically abnormal preimplantation embryos, using combinations of specific primers for chromosomes 9, 13, 16, 18, 21, X, and Y.
Embryos were obtained from patients at the Montpellier University Hospital.
PATIENT(S): Seven women undergoing IVF at the Montpellier University Hospital.
INTERVENTION(S): Isolated interphase nuclei from poor quality preimplantation embryos were prepared for primed in situ labeling technique.
MAIN OUTCOME MEASURE(S): Numerical abnormalities assessed by primed in situ labeling analysis.
RESULT(S): Using directly fluorescent-labeled nucleotides, the labeling reaction for three chromosomes did not exceed 2.30 hours. Only three analyzed embryos appeared to be chromosomally normal. Mosaicism, aneupoidy, and haploidy were observed in the seven other embryos.
CONCLUSION(S): The primed in situ labeling method offers a simple and reliable screening tool for gender determination and aneuploidy detection. The use of this technique may contribute to significantly improve the procedure of preimplantation diagnosis.
介绍引物原位标记法在植入前诊断中的应用。
对10个形态异常的植入前胚胎进行双引物和三引物原位标记,使用针对9号、13号、16号、18号、21号染色体、X染色体和Y染色体的特异性引物组合。
胚胎取自蒙彼利埃大学医院的患者。
7名在蒙彼利埃大学医院接受体外受精的女性。
为引物原位标记技术制备来自质量差的植入前胚胎的分离间期核。
通过引物原位标记分析评估的数目异常。
使用直接荧光标记的核苷酸,三条染色体的标记反应不超过2.30小时。仅三个分析的胚胎似乎染色体正常。在其他七个胚胎中观察到嵌合体、非整倍体和单倍体。
引物原位标记法为性别鉴定和非整倍体检测提供了一种简单可靠的筛查工具。该技术的应用可能有助于显著改进植入前诊断程序。