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应用两轮荧光原位杂交进行人类植入前胚胎染色体嵌合型的研究
引用本文:任秀莲,徐艳文,周灿权,庄广伦.应用两轮荧光原位杂交进行人类植入前胚胎染色体嵌合型的研究[J].中华医学遗传学杂志,2007,24(6):706-708.
作者姓名:任秀莲  徐艳文  周灿权  庄广伦
作者单位:1. 北京大学第三医院生殖中心,100083
2. 中山大学附属第一医院生殖中心,广州,510080
摘    要:目的应用2轮荧光原位杂交技术(fluorescence in situ hybridization,FISH)对人类植入前胚胎染色体嵌合型的发生机制和影响因素进行初步研究。方法选择体外受精与胚胎移植(in vitro fertilization-embryo transplantation,IVF-ET)治疗周期中不适于胚胎移植和冷冻的正常受精胚胎为研究对象,固定后进行2轮FISH,分析13、16、18、21、22、X、Y等7条染色体组成。结果51个胚胎中正常胚胎14个(27.5%),嵌合型16个(31.4%),无规律分裂12个(23.5%),异常非嵌合型9个(17.6%)。5~8细胞期胚胎中嵌合型胚胎的比例显著高于≤4细胞期胚胎(40.0%比12.5%)。非整倍体胚胎的比率在≥35岁组为57.1%,显著高于<35岁组(23.3%)。结论胚胎染色体嵌合型是植入前胚胎的常见现象,可能是影响IVF成功率的重要因素,而应用2轮FISH技术可有效地进行常见染色体异常的筛查。

关 键 词:荧光原位杂交  嵌合型  植入前遗传学诊断
收稿时间:2007-01-21

Analysis of chromosome mosaicism in preimplantation embryos by using 2 sequential rounds of fluorescence in situ hybridization
REN Xiu-lian,XU Yan-wen,ZHOU Can-quan,ZHUANG Guang-lun.Analysis of chromosome mosaicism in preimplantation embryos by using 2 sequential rounds of fluorescence in situ hybridization[J].Chinese Journal of Medical Genetics,2007,24(6):706-708.
Authors:REN Xiu-lian  XU Yan-wen  ZHOU Can-quan  ZHUANG Guang-lun
Institution:Reproductive Medical Center, the First Affiliated Hospital, SUN Yat-sen University, Guangzhou, Guangdong, 510080 PR China.
Abstract:OBJECTIVE: To investigate the mechanism and factors affecting mosaicism in human preimplantation embryos by using 2 sequential rounds of fluorescence in situ hybridization(FISH). METHODS: Totally 51 normal fertilized embryos, which were not suitable for embryo transfer and cryopreservation, were analyzed on day 3 after fertilization by using two sequential rounds of FISH. Chromosomes 13, 16, 18, 21, 22, X and Y were analyzed. RESULTS: Among 51 embryos, 16 (31.4%) were mosaic, 12 (23.5%) were chaotic, and the remaining were either normal (27.5%) or non-mosaic abnormal (17.6%). The incidence of mosaic embryos was related to embryo developmental stage, for the incidence of mosaicism increased from 12.5% in embryos
Keywords:fluorescence in situ hybridization  mosaicism  preimplantation genetic diagnosis
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