Fast Quantitative Real-Time PCR-Based Screening for Common Chromosomal Aneuploidies in Mouse Embryonic Stem Cells

被引:14
作者
D'Hulst, Charlotte
Parvanova, Irena
Tomoiaga, Delia
Sapar, Maria L.
Feinstein, Paul [1 ]
机构
[1] CUNY, Hunter Coll, Dept Biol Sci, New York, NY 10065 USA
来源
STEM CELL REPORTS | 2013年 / 1卷 / 04期
关键词
POLYMERASE-CHAIN-REACTION; ZYGOSITY DETERMINATION; MICE; GENOME; LINES; TRANSCRIPTION; TRISOMY-8;
D O I
10.1016/j.stemcr.2013.08.003
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Chromosomal integrity has been known for many years to affect the ability of mouse embryonic stem cells (mESCs) to contribute to the germline of chimeric mice. Abnormal chromosomes are generally detected by standard cytogenetic karyotyping. However, this method is expensive, time consuming, and often omitted prior to blastocyst injection, consequently reducing the frequency of mESC-derived offspring. Here, we show a fast, accurate, and inexpensive screen for identifying the two most common aneuploidies (Trisomy 8 and loss of chromosome Y) in genetically manipulated mESCs using quantitative real-time PCR (qPCR). Screening against these two aneuploidies significantly increases the fraction of normal mESC clones. Our method is extremely sensitive and can detect as low as 10% aneuploidy among a large population of mESCs. It greatly expedites the generation of mutant mice and provides a quick tool for assessing the aneuploidy percentages of any mESC line.
引用
收藏
页码:350 / 359
页数:10
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