Korstanje Ron, Desai Jigar, Lazar Gloria, King Benjamin, Rollins Jarod, Spurr Melissa, Joseph Jamie, Kadambi Sindhuja, Li Yang, Cherry Allison, Matteson Paul G, Paigen Beverly, Millonig James H
Jackson Laboratory, Bar Harbor, Maine, USA.
Physiol Genomics. 2008 Nov 12;35(3):296-304. doi: 10.1152/physiolgenomics.90260.2008. Epub 2008 Sep 16.
The vacuolated lens (vl) mouse mutant arose spontaneously on the C3H/HeSn background and exhibits neural tube defects (NTDs), congenital cataract, and occasionally a white belly spot. We previously reported that 1) the vl phenotypes are due to a mutation in an orphan G protein-coupled receptor (GPCR), Gpr161; 2) the penetrance of the vl NTD and cataract phenotypes are affected by genetic background, allowing three unlinked quantitative trait loci (QTL) to be mapped (modifiers of vacuolated lens, Modvl1-3); and 3) phenotype-based bioinformatics followed by genetic and molecular analysis identified a lens-specific transcription factor that contributes to the cataract-modifying effect of Modvl3. We now extend this analysis in three ways. First, using the Gpr161 mutation to unequivocally identify mutant adults and embryos, we determined that approximately 50% of vl/vl NTD-affected embryos die during development. Second, the MOLF/Ei genetic background suppresses this embryonic lethality but increases the incidence of the adult belly spot phenotype. Additional QTL analysis was performed, and two novel modifiers were mapped [Modvl4, logarithm of odds ratio (LOD) 4.4; Modvl5, LOD 5.0]. Third, phenotype-based bioinformatics identified candidate genes for these modifiers including two GPCRs that cause NTD or skin/pigmentation defects (Modvl4: Frizzled homolog 6; Modvl5: Melanocortin 5 receptor). Because GPCRs form oligomeric complexes, these genes were resequenced and nonsynonymous coding variants were identified. Bioinformatics and protein modeling suggest that these variants may be functional. Our studies further establish vl as a multigenic mouse model for NTDs and identify additional QTL that interact with Gpr161 to regulate neurulation.
空泡晶状体(vl)小鼠突变体在C3H/HeSn背景上自发产生,表现出神经管缺陷(NTDs)、先天性白内障,偶尔还有白色腹部斑点。我们之前报道过:1)vl表型是由于一个孤儿G蛋白偶联受体(GPCR)Gpr161发生突变所致;2)vl NTD和白内障表型的外显率受遗传背景影响,从而定位到三个不连锁的数量性状基因座(QTL)(空泡晶状体修饰基因,Modvl1 - 3);3)基于表型的生物信息学分析,随后进行遗传和分子分析,确定了一种晶状体特异性转录因子,它对Modvl3的白内障修饰作用有贡献。我们现在通过三种方式扩展了这一分析。首先,利用Gpr161突变明确鉴定突变的成年小鼠和胚胎,我们确定约50%受NTD影响的vl/vl胚胎在发育过程中死亡。其次,MOLF/Ei遗传背景抑制了这种胚胎致死性,但增加了成年腹部斑点表型的发生率。进行了额外的QTL分析,并定位到两个新的修饰基因[Modvl4,优势对数比(LOD)4.4;Modvl5,LOD 5.0]。第三,基于表型的生物信息学确定了这些修饰基因的候选基因,包括两个导致NTD或皮肤/色素沉着缺陷的GPCR(Modvl4:卷曲同源物6;Modvl5:黑皮质素5受体)。由于GPCR形成寡聚体复合物,对这些基因进行了重测序,并鉴定出非同义编码变体。生物信息学和蛋白质建模表明这些变体可能具有功能。我们的研究进一步将vl确立为NTDs的多基因小鼠模型,并鉴定出与Gpr161相互作用以调节神经胚形成的其他QTL。