Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters

被引:18
作者
Aigner, Bernhard [1 ,2 ]
Rathkolb, Birgit [1 ,2 ]
Klempt, Martina [1 ,2 ]
Wagner, Sibylle [3 ,4 ]
Michel, Dian [3 ,4 ]
Klaften, Matthias [3 ,4 ]
Laufs, Juergen [5 ]
Schneider, Boris [5 ]
Sedlmeier, Reinhard [5 ]
de Angelis, Martin Hrabe [3 ,4 ]
Wolf, Eckhard [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Vet Sci, Chair Mol Anim Breeding & Biotechnol, D-85764 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, LAFUGA, Gene Ctr, D-85764 Munich, Germany
[3] Helmholtz Zentrum Munchen, Inst Expt Genet, Neuherberg, Germany
[4] Tech Univ Munich, Chair Expt Genet, Helmholtz Zentrum Munchen, Neuherberg, Germany
[5] Ingenium Pharmaceut, Martinsried, Germany
关键词
MULTIPLE INTESTINAL NEOPLASIA; GENOME-WIDE; TRANSFERRIN RECEPTOR; PHENOTYPE-DRIVEN; ENU MUTAGENESIS; POINT MUTATION; MPL(-/-) MICE; C-MYB; GENE; THROMBOCYTOPENIA;
D O I
10.1007/s00335-011-9328-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Research on hematological disorders relies on suitable animal models. We retrospectively evaluated the use of the hematological parameters hematocrit (HCT), hemoglobin (HGB), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), mean corpuscular volume (MCV), red blood cell count (RBC), white blood cell count (WBC), and platelet count (PLT) in the phenotype-driven Munich N-ethyl-N-nitrosourea (ENU) mouse mutagenesis project as parameters for the generation of novel animal models for human diseases. The analysis was carried out on more than 16,000 G1 and G3 offspring of chemically mutagenized inbred C3H mice to detect dominant and recessive mutations leading to deviations in the levels of the chosen parameters. Identification of animals exhibiting altered values and transmission of the phenotypic deviations to the subsequent generations led to the successful establishment of mutant lines for the parameters MCV, RBC, and PLT. Analysis of the causative mutation was started in selected lines, thereby revealing a novel mutation in the transferrin receptor gene (Tfrc) in one line. Thus, novel phenotype-driven mouse models were established to analyze the genetic components of hematological disorders.
引用
收藏
页码:495 / 505
页数:11
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