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乘客突变混淆了所有基因改造近交系小鼠的解读。

Passenger Mutations Confound Interpretation of All Genetically Modified Congenic Mice.

作者信息

Vanden Berghe Tom, Hulpiau Paco, Martens Liesbet, Vandenbroucke Roosmarijn E, Van Wonterghem Elien, Perry Seth W, Bruggeman Inge, Divert Tatyana, Choi Sze Men, Vuylsteke Marnik, Shestopalov Valery I, Libert Claude, Vandenabeele Peter

机构信息

Inflammation Research Center, VIB, 9000 Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, 9000 Ghent, Belgium.

Inflammation Research Center, VIB, 9000 Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, 9000 Ghent, Belgium.

出版信息

Immunity. 2015 Jul 21;43(1):200-9. doi: 10.1016/j.immuni.2015.06.011. Epub 2015 Jul 7.

Abstract

Targeted mutagenesis in mice is a powerful tool for functional analysis of genes. However, genetic variation between embryonic stem cells (ESCs) used for targeting (previously almost exclusively 129-derived) and recipient strains (often C57BL/6J) typically results in congenic mice in which the targeted gene is flanked by ESC-derived passenger DNA potentially containing mutations. Comparative genomic analysis of 129 and C57BL/6J mouse strains revealed indels and single nucleotide polymorphisms resulting in alternative or aberrant amino acid sequences in 1,084 genes in the 129-strain genome. Annotating these passenger mutations to the reported genetically modified congenic mice that were generated using 129-strain ESCs revealed that nearly all these mice possess multiple passenger mutations potentially influencing the phenotypic outcome. We illustrated this phenotypic interference of 129-derived passenger mutations with several case studies and developed a Me-PaMuFind-It web tool to estimate the number and possible effect of passenger mutations in transgenic mice of interest.

摘要

小鼠中的靶向诱变是基因功能分析的强大工具。然而,用于靶向的胚胎干细胞(ESC,以前几乎都是源自129品系)与受体品系(通常是C57BL/6J)之间的遗传变异通常会导致同源基因小鼠,其中靶向基因两侧是可能含有突变的ESC衍生的乘客DNA。对129和C57BL/6J小鼠品系的比较基因组分析揭示了插入缺失和单核苷酸多态性,导致129品系基因组中的1084个基因出现替代或异常氨基酸序列。对使用129品系ESC产生的已报道的基因改造同源基因小鼠的这些乘客突变进行注释后发现,几乎所有这些小鼠都具有多个可能影响表型结果的乘客突变。我们通过几个案例研究说明了源自129的乘客突变的这种表型干扰,并开发了一个Me-PaMuFind-It网络工具来估计感兴趣的转基因小鼠中乘客突变的数量和可能的影响。

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