| First Author | Noguchi Y | Year | 2006 |
| Journal | Genetics | Volume | 173 |
| Issue | 4 | Pages | 2111-9 |
| PubMed ID | 16648588 | Mgi Jnum | J:111838 |
| Mgi Id | MGI:3654953 | Doi | 10.1534/genetics.106.057372 |
| Citation | Noguchi Y, et al. (2006) Multiple Quantitative Trait Loci Modify Cochlear Hair Cell Degeneration in the Beethoven (Tmc1Bth) Mouse Model of Progressive Hearing Loss DFNA36. Genetics 173(4):2111-9 |
| abstractText | Dominant mutations of transmembrane channel-like gene 1 (TMC1) cause progressive sensorineural hearing loss in humans and Beethoven (Tmc1(Bth/+)) mice. Here we show that Tmc1(Bth/+) mice on a C3HeB/FeJ strain background have selective degeneration of inner hair cells while outer hair cells remain structurally and functionally intact. Inner hair cells primarily function as afferent sensory cells, whereas outer hair cells are electromotile amplifiers of auditory stimuli that can be functionally assessed by distortion product otoacoustic emission (DPOAE) analysis. When C3H-Tmc1(Bth/Bth) is crossed with either C57BL/6J or DBA/2J wild-type mice, F(1) hybrid Tmc1(Bth/+) progeny have increased hearing loss associated with increased degeneration of outer hair cells and diminution of DPOAE amplitudes but no difference in degeneration of inner hair cells. We mapped at least one quantitative trait locus (QTL), Tmc1m1, for DPOAE amplitude on chromosome 2 in [(C/B)F(1) x C]N(2)-Tmc1(Bth/+) backcross progeny, and three other QTL on chromosomes 11 (Tmc1m2), 12 (Tmc1m3), and 5 (Tmc1m4) in [(C/D)F(1) x C]N(2)-Tmc1(Bth/+) progeny. The polygenic basis of outer hair cell degeneration in Beethoven mice provides a model system for the dissection of common, complex hearing loss phenotypes, such as presbycusis, that involve outer hair cell degeneration in humans. |
