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PMID:19414487

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Citation

Geng, R, Geller, SF, Hayashi, T, Ray, CA, Reh, TA, Bermingham-McDonogh, O, Jones, SM, Wright, CG, Melki, S, Imanishi, Y, Palczewski, K, Alagramam, KN and Flannery, JG (2009) Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation. Hum. Mol. Genet. 18:2748-60

Abstract

Usher syndrome 3A (USH3A) is an autosomal recessive disorder characterized by progressive loss of hearing and vision due to mutation in the clarin-1 (CLRN1) gene. Lack of an animal model has hindered our ability to understand the function of CLRN1 and the pathophysiology associated with USH3A. Here we report for the first time a mouse model for ear disease in USH3A. Detailed evaluation of inner ear phenotype in the Clrn1 knockout mouse (Clrn1(-/-)) coupled with expression pattern of Clrn1 in the inner ear are presented here. Clrn1 was expressed as early as embryonic day 16.5 in the auditory and vestibular hair cells and associated ganglionic neurons, with its expression being higher in outer hair cells (OHCs) than inner hair cells. Clrn1(-/-) mice showed early onset hearing loss that rapidly progressed to severe levels. Two to three weeks after birth (P14-P21), Clrn1(-/-) mice showed elevated auditory-evoked brainstem response (ABR) thresholds and prolonged peak and interpeak latencies. By P21, approximately 70% of Clrn1(-/-) mice had no detectable ABR and by P30 these mice were deaf. Distortion product otoacoustic emissions were not recordable from Clrn1(-/-) mice. Vestibular function in Clrn1(-/-) mice mirrored the cochlear phenotype, although it deteriorated more gradually than cochlear function. Disorganization of OHC stereocilia was seen as early as P2 and by P21 OHC loss was observed. In sum, hair cell dysfunction and prolonged peak latencies in vestibular and cochlear evoked potentials in Clrn1(-/-) mice strongly indicate that Clrn1 is necessary for hair cell function and associated neural activation.

Links

PubMed PMC2706682 Online version:10.1093/hmg/ddp210

Keywords

Animals; Disease Models, Animal; Female; Hair Cells, Auditory/physiology; Humans; Male; Membrane Proteins/genetics; Membrane Proteins/metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Neurons/physiology; Usher Syndromes/genetics; Usher Syndromes/metabolism; Usher Syndromes/physiopathology

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

MOUSE:CLRN1

acts_upstream_of_or_within

GO:0007605: sensory perception of sound

ECO:0000315: mutant phenotype evidence used in manual assertion

MGI:MGI:3850171

P

Seeded From UniProt

complete

MOUSE:CLRN1

acts_upstream_of_or_within

GO:0050885: neuromuscular process controlling balance

ECO:0000315: mutant phenotype evidence used in manual assertion

MGI:MGI:3850171

P

Seeded From UniProt

complete

MOUSE:CLRN1

acts_upstream_of_or_within

GO:0060117: auditory receptor cell development

ECO:0000315: mutant phenotype evidence used in manual assertion

MGI:MGI:3850171

P

  • results_in_development_of:(CL:0000589)|results_in_development_of:(CL:0000601)

Seeded From UniProt

complete

MOUSE:CLRN1

acts_upstream_of_or_within

GO:0060088: auditory receptor cell stereocilium organization

ECO:0000315: mutant phenotype evidence used in manual assertion

MGI:MGI:3850171

P

Seeded From UniProt

complete


See also

References

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