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Oligonucleotide Arrays vs. Metaphase-Comparative Genomic Hybridisation and BAC Arrays for Single-Cell Analysis: First Applications to Preimplantation Genetic Diagnosis for Robertsonian Translocation Carriers

机译:寡核苷酸阵列与单细胞分析的中期比较基因组杂交和BAC阵列:罗伯逊易位携带者的植入前遗传学诊断的首次应用。

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摘要

Comprehensive chromosome analysis techniques such as metaphase-Comparative Genomic Hybridisation (CGH) and array-CGH are available for single-cell analysis. However, while metaphase-CGH and BAC array-CGH have been widely used for Preimplantation Genetic Diagnosis, oligonucleotide array-CGH has not been used in an extensive way. A comparison between oligonucleotide array-CGH and metaphase-CGH has been performed analysing 15 single fibroblasts from aneuploid cell-lines and 18 single blastomeres from human cleavage-stage embryos. Afterwards, oligonucleotide array-CGH and BAC array-CGH were also compared analysing 16 single blastomeres from human cleavage-stage embryos. All three comprehensive analysis techniques provided broadly similar cytogenetic profiles; however, non-identical profiles appeared when extensive aneuploidies were present in a cell. Both array techniques provided an optimised analysis procedure and a higher resolution than metaphase-CGH. Moreover, oligonucleotide array-CGH was able to define extra segmental imbalances in 14.7% of the blastomeres and it better determined the specific unbalanced chromosome regions due to a higher resolution of the technique (≈20 kb). Applicability of oligonucleotide array-CGH for Preimplantation Genetic Diagnosis has been demonstrated in two cases of Robertsonian translocation carriers 45,XY,der(13;14)(q10;q10). Transfer of euploid embryos was performed in both cases and pregnancy was achieved by one of the couples. This is the first time that an oligonucleotide array-CGH approach has been successfully applied to Preimplantation Genetic Diagnosis for balanced chromosome rearrangement carriers.
机译:诸如中期比较基因组杂交(CGH)和阵列CGH之类的综合染色体分析技术可用于单细胞分析。然而,尽管中期-CGH和BAC阵列-CGH已广泛用于植入前遗传诊断,但是寡核苷酸阵列-CGH尚未得到广泛使用。在寡核苷酸阵列-CGH和中期-CGH之间进行了比较,分析了来自非整倍体细胞系的15个单纤维细胞和来自人类卵裂期胚胎的18个单卵裂球。之后,还比较了寡核苷酸阵列-CGH和BAC阵列-CGH,分析了人类卵裂期胚胎的16个单卵裂球。所有这三种综合分析技术均提供了大致相似的细胞遗传学特征。但是,当细胞中存在大量非整倍性时,会出现不同的曲线。与中期CGH相比,两种阵列技术均提供了优化的分析程序和更高的分辨率。此外,寡核苷酸阵列-CGH能够在14.7%的卵裂球中定义额外的节段失衡,并且由于该技术的更高分辨率(≈20kb),它可以更好地确定特定的不平衡染色体区域。已经在两种罗伯逊易位载体45,XY,der(13; 14)(q10; q10)中证明了寡核苷酸阵列-CGH在植入前遗传学诊断中的适用性。在这两种情况下均进行了整倍体胚胎的转移,其中一对夫妻实现了妊娠。这是寡核苷酸阵列-CGH方法首次成功用于平衡染色体重排载体的植入前遗传学诊断。

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