Mohlke K L, Nichols W C, Westrick R J, Novak E K, Cooney K A, Swank R T, Ginsburg D
Department of Human Genetics, University of Michigan Medical School, Ann Arbor 48109, USA.
Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15352-7. doi: 10.1073/pnas.93.26.15352.
Type 1 von Willebrand disease (VWD), characterized by reduced levels of plasma von Willebrand factor (VWF), is the most common inherited bleeding disorder in humans. Penetrance of VWD is incomplete, and expression of the bleeding phenotype is highly variable. In addition, plasma VWF levels vary widely among normal individuals. To identify genes that influence VWF level, we analyzed a genetic cross between RIIIS/J and CASA/Rk, two strains of mice that exhibit a 20-fold difference in plasma VWF level. DNA samples from F2 progeny demonstrating either extremely high or extremely low plasma VWF levels were pooled and genotyped for 41 markers spanning the autosomal genome. A novel locus accounting for 63% of the total variance in VWF level was mapped to distal mouse chromosome 11, which is distinct from the murine Vwf locus on chromosome 6. We designated this locus Mvwf for "modifier of VWF." Additional genotyping of as many as 2407 meioses established a high resolution genetic map with gene order Cola1-Itg3a-Ngfr-Mvwf/Gip-Hoxb9-Hoxb1++ +-Cbx'rs2-Cox5a-Gfap. The Mvwf candidate interval between Ngfr and Hoxb9 is approximately 0.5 centimorgan (cM). These results demonstrate that a single dominant gene accounts for the low VWF phenotype of RIIIS/J mice in crosses with several other strains. The pattern of inheritance suggests a gain-of-function mutation in a unique component of VWF biosynthesis or processing. Characterization of the human homologue for Mvwf may have relevance for a subset of type 1 VWD cases and may define an important genetic factor modifying penetrance and expression of mutations at the VWF locus.
1型血管性血友病(VWD)的特征是血浆血管性血友病因子(VWF)水平降低,它是人类最常见的遗传性出血性疾病。VWD的外显率不完全,出血表型的表达高度可变。此外,正常个体之间的血浆VWF水平差异很大。为了鉴定影响VWF水平的基因,我们分析了RIIIS/J和CASA/Rk这两种小鼠品系之间的遗传杂交,这两种小鼠的血浆VWF水平相差20倍。将表现出极高或极低血浆VWF水平的F2后代的DNA样本进行合并,并对跨越常染色体基因组的41个标记进行基因分型。一个新的位点被定位到小鼠11号染色体远端,该位点解释了VWF水平总变异的63%,它与6号染色体上的小鼠Vwf位点不同。我们将这个位点命名为Mvwf,即“VWF的修饰基因”。对多达2407次减数分裂进行的额外基因分型建立了一个高分辨率遗传图谱,基因顺序为Cola1-Itg3a-Ngfr-Mvwf/Gip-Hoxb9-Hoxb1++ +-Cbx'rs2-Cox5a-Gfap。Ngfr和Hoxb9之间的Mvwf候选区间约为0.5厘摩(cM)。这些结果表明,在与其他几个品系杂交时,单个显性基因导致了RIIIS/J小鼠的低VWF表型。遗传模式表明在VWF生物合成或加工的一个独特成分中存在功能获得性突变。对Mvwf人类同源物的表征可能与一部分1型VWD病例相关,并且可能定义一个修饰VWF位点突变的外显率和表达的重要遗传因素。