The chronic proliferative dermatitis mouse mutation (cpdm): mapping of the mutant gene locus

John P. Sundberg , Dawnalyn Boggess , Leonard D. Shultz , Remond J.A. Fijneman , Peter Demant , Harm Hogenesch , Gregory A. Cox
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引用次数: 4

Abstract

The chronic proliferative dermatitis (cpdm) mouse mutation was mapped to mouse Chromosome 15 using an intraspecific cross between C57BL/KaLawRij cpdm/cpdm and BALB/cJ mice. A second autosomal recessive mutation that resulted in a phenotype similar to that of cpdm arose spontaneously in a colony of OcB-3/Dem recombinant congenic mice. This new mutation was found to be allelic with cpdm. Therefore, the gene symbol for the allelic mutation is cpdmDem. The phenotype of these mutant mice consists of eosinophil-driven severe and progressive inflammatory changes in multiple organs including the skin and lungs.

慢性增生性皮炎小鼠突变(cpdm):突变基因位点的定位
利用C57BL/KaLawRij cpdm/cpdm与BALB/cJ小鼠的种内杂交,将慢性增生性皮炎(cpdm)小鼠突变定位到小鼠15号染色体上。在OcB-3/Dem重组基因小鼠群体中自发产生了第二个常染色体隐性突变,导致与cpdm相似的表型。这个新的突变被发现与cpdm等位。因此,该等位基因突变的基因符号为cpdmDem。这些突变小鼠的表型包括嗜酸性粒细胞驱动的包括皮肤和肺在内的多个器官的严重和进行性炎症变化。
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