Cheverud J M, Lawson H A, Bouckaert K, Kossenkov A V, Showe L C, Cort L, Blankenhorn E P, Bedelbaeva K, Gourevitch D, Zhang Y, Heber-Katz E
Department of Anatomy and Neurobiology, Washington University School of Medicine, St Louis, MO, USA.
Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia, PA, USA.
Heredity (Edinb). 2014 May;112(5):508-18. doi: 10.1038/hdy.2013.133. Epub 2014 Feb 26.
External ear hole closure in LG/J mice represents a model of regenerative response. It is accompanied by the formation of a blastema-like structure and the re-growth of multiple tissues, including cartilage. The ability to regenerate tissue is heritable. An F34 advanced intercross line of mice (Wustl:LG,SM-G34) was generated to identify genomic loci involved in ear hole closure over a 30-day healing period. We mapped 19 quantitative trait loci (QTL) for ear hole closure. Individual gene effects are relatively small (0.08 mm), and most loci have co-dominant effects with phenotypically intermediate heterozygotes. QTL support regions were limited to a median size of 2 Mb containing a median of 19 genes. Positional candidate genes were evaluated using differential transcript expression between LG/J and SM/J healing tissue, function analysis and bioinformatic analysis of single-nucleotide polymorphisms in and around positional candidate genes of interest. Analysis of the set of 34 positional candidate genes and those displaying expression differences revealed over-representation of genes involved in cell cycle regulation/DNA damage, cell migration and adhesion, developmentally related genes and metabolism. This indicates that the healing phenotype in LG/J mice involves multiple physiological mechanisms.
LG/J小鼠的外耳道闭合代表了一种再生反应模型。它伴随着芽基样结构的形成以及包括软骨在内的多种组织的再生。组织再生能力是可遗传的。为了确定在30天愈合期内参与耳孔闭合的基因组位点,构建了一个F34小鼠高级杂交系(Wustl:LG,SM-G34)。我们绘制了19个耳孔闭合的数量性状位点(QTL)。单个基因的效应相对较小(0.08毫米),并且大多数位点对表型中间杂合子具有共显性效应。QTL支持区域的中位数大小限制在2兆碱基,其中包含中位数为19个基因。使用LG/J和SM/J愈合组织之间的差异转录本表达、功能分析以及感兴趣的位置候选基因及其周围单核苷酸多态性的生物信息学分析来评估位置候选基因。对34个位置候选基因以及那些显示表达差异的基因进行分析,发现参与细胞周期调控/DNA损伤、细胞迁移和黏附以及发育相关基因和代谢的基因存在过度表达。这表明LG/J小鼠的愈合表型涉及多种生理机制。