Literature DB >> 26163370

Passenger Mutations Confound Interpretation of All Genetically Modified Congenic Mice.

Tom Vanden Berghe1, Paco Hulpiau2, Liesbet Martens2, Roosmarijn E Vandenbroucke2, Elien Van Wonterghem2, Seth W Perry3, Inge Bruggeman2, Tatyana Divert2, Sze Men Choi2, Marnik Vuylsteke4, Valery I Shestopalov5, Claude Libert2, Peter Vandenabeele6.   

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.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26163370      PMCID: PMC4800811          DOI: 10.1016/j.immuni.2015.06.011

Source DB:  PubMed          Journal:  Immunity        ISSN: 1074-7613            Impact factor:   31.745


  46 in total

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Review 3.  PRMT7 as a unique member of the protein arginine methyltransferase family: A review.

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9.  Intracellular Nucleic Acid Sensing Triggers Necroptosis through Synergistic Type I IFN and TNF Signaling.

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10.  The AIM2-like Receptors Are Dispensable for the Interferon Response to Intracellular DNA.

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