Tian Cong, Gagnon Leona H, Longo-Guess Chantal, Korstanje Ron, Sheehan Susan M, Ohlemiller Kevin K, Schrader Angela D, Lett Jaclynn M, Johnson Kenneth R
The Jackson Laboratory, Bar Harbor, ME 04609, USA.
Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, ME 04469, USA.
Hum Mol Genet. 2017 Oct 1;26(19):3722-3735. doi: 10.1093/hmg/ddx257.
Mutations of the human ATP6V1B1 gene cause distal renal tubular acidosis (dRTA; OMIM #267300) often associated with sensorineural hearing impairment; however, mice with a knockout mutation of Atp6v1b1 were reported to exhibit a compensated acidosis and normal hearing. We discovered a new spontaneous mutation (vortex, symbol vtx) of Atp6v1b1 in an MRL/MpJ (MRL) colony of mice. In contrast to the reported phenotype of the knockout mouse, which was developed on a primarily C57BL/6 (B6) strain background, MRL-Atp6v1b1vtx/vtx mutant mice exhibit profound hearing impairment, which is associated with enlarged endolymphatic compartments of the inner ear. Mutant mice have alkaline urine but do not exhibit overt metabolic acidosis, a renal phenotype similar to that of the Atpbv1b1 knockout mouse. The abnormal inner ear phenotype of MRL- Atp6v1b1vtx/vtx mice was lost when the mutation was transferred onto the C57BL/6J (B6) background, indicating the influence of strain-specific genetic modifiers. To genetically map modifier loci in Atp6v1b1vtx/vtx mice, we analysed ABR thresholds of progeny from a backcross segregating MRL and B6 alleles. We found statistically significant linkage with a locus on Chr 13 that accounts for about 20% of the hearing threshold variation in the backcross mice. The important effect that genetic background has on the inner ear phenotype of Atp6v1b1 mutant mice provides insight into the hearing loss variability associated with dRTA caused by ATP6V1B1 mutations. Because MRL-Atp6v1b1vxt/vtx mice do not recapitulate the metabolic acidosis of dRTA patients, they provide a new genetic model for nonsyndromic deafness with enlarged vestibular aqueduct (EVA; OMIM #600791).
人类ATP6V1B1基因突变会导致远端肾小管酸中毒(dRTA;OMIM #267300),常伴有感音神经性听力障碍;然而,据报道,Atp6v1b1基因敲除突变的小鼠表现为代偿性酸中毒且听力正常。我们在MRL/MpJ(MRL)小鼠品系中发现了Atp6v1b1基因的一个新的自发突变(漩涡,符号为vtx)。与报道的在主要C57BL/6(B6)品系背景上培育的基因敲除小鼠的表型不同,MRL-Atp6v1b1vtx/vtx突变小鼠表现出严重的听力障碍,这与内耳内淋巴腔扩大有关。突变小鼠尿液呈碱性,但未表现出明显的代谢性酸中毒,其肾脏表型与Atpbv1b1基因敲除小鼠相似。当该突变转移到C57BL/6J(B6)背景上时,MRL-Atp6v1b1vtx/vtx小鼠异常的内耳表型消失了,这表明了品系特异性遗传修饰因子的影响。为了对Atp6v1b1vtx/vtx小鼠中的修饰基因座进行遗传定位,我们分析了回交后代中分离MRL和B6等位基因的听性脑干反应(ABR)阈值。我们发现与13号染色体上的一个基因座存在统计学上的显著连锁,该基因座约占回交小鼠听力阈值变异的20%。遗传背景对Atp6v1b1突变小鼠内耳表型的重要影响为深入了解由ATP6V1B1突变引起的dRTA相关听力损失的变异性提供了线索。由于MRL-Atp6v1b1vxt/vtx小鼠不能重现dRTA患者的代谢性酸中毒,它们为伴有前庭导水管扩大(EVA;OMIM #600791)的非综合征性耳聋提供了一种新的遗传模型。