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使用克隆胚胎活检评估 MDA 效率进行基因分型。

Assessment of MDA efficiency for genotyping using cloned embryo biopsies.

机构信息

Parco Tecnologico Padano, Via Einstein, Lodi, Italy.

出版信息

Genomics. 2013 Jan;101(1):24-9. doi: 10.1016/j.ygeno.2012.09.002. Epub 2012 Sep 12.

Abstract

The possibility to genotype embryos prior to implantation would have advantages for increasing the speed of selection of cattle. Reliable genotyping requires more DNA than can be obtained from biopsies of embryos, if they are to remain viable. Multiple displacement amplification (MDA) is a whole genome amplification technique used to increase the amount of DNA from biopsies for analysis. Reduced genome coverage resulting in Allele Drop Out (ADO) at heterozygous loci or missing genotypes are drawbacks of MDA. The present article describes the correlation between the input DNA quantity or embryo biopsy size and MDA success. Missing genotypes and ADO drastically increased when fewer than 30-40 cells or the genomic equivalents were used. However, embryo viability was found to be reduced if biopsied with more than 10 cells. Therefore, in vitro cell culture was investigated as a means to increase the number of cells available and the genotyping reliability.

摘要

在胚胎植入前进行基因分型的可能性将有利于提高牛的选择速度。如果要使胚胎保持活力,可靠的基因分型需要比从胚胎活检中获得的更多的 DNA。多重置换扩增(MDA)是一种全基因组扩增技术,用于增加活检的 DNA 量以进行分析。在杂合子位点导致等位基因丢失(ADO)或缺失基因型的基因组覆盖度降低是 MDA 的缺点。本文描述了输入 DNA 量或胚胎活检大小与 MDA 成功之间的相关性。当使用少于 30-40 个细胞或基因组当量时,缺失的基因型和 ADO 急剧增加。然而,如果活检使用超过 10 个细胞,则发现胚胎活力降低。因此,研究了体外细胞培养作为增加可用细胞数量和基因分型可靠性的一种手段。

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