A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination

Marina R Carpinelli, Anne K Voss, Michael G Manning, Ashwyn A Perera, Anne A Cooray, Benjamin T Kile, Rachel A Burt

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Canavan disease is a leukodystrophy caused by mutations in the ASPA gene. This gene encodes the enzyme that converts N-acetylaspartate into acetate and aspartic acid. In Canavan disease, spongiform encephalopathy of the brain causes progressive mental retardation, motor deficit and death. We have isolated a mouse with a novel ethylnitrosourea-induced mutation in Aspa. This mutant, named deaf14, carries a c.516T>A mutation that is predicted to cause a p.Y172X protein truncation. No full-length ASPA protein is produced in deaf14 brain and there is extensive spongy degeneration. Interestingly, we found that deaf14 mice have an attenuated startle in response to loud noise. The first auditory brainstem response peak has normal latency and amplitude but peaks II, III, IV and V have increased latency and decreased amplitude in deaf14 mice. Our work reveals a hitherto unappreciated pathology in a mouse model of Canavan disease, implying that auditory brainstem response testing could be used in diagnosis and to monitor the progression of this disease.
Original languageEnglish
Pages (from-to)649-657
Number of pages9
JournalDisease Models and Mechanisms
Volume7
Issue number6
DOIs
Publication statusPublished - 2014
Externally publishedYes

Cite this

Carpinelli, Marina R ; Voss, Anne K ; Manning, Michael G ; Perera, Ashwyn A ; Cooray, Anne A ; Kile, Benjamin T ; Burt, Rachel A. / A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination. In: Disease Models and Mechanisms. 2014 ; Vol. 7, No. 6. pp. 649-657.
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title = "A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination",
abstract = "Canavan disease is a leukodystrophy caused by mutations in the ASPA gene. This gene encodes the enzyme that converts N-acetylaspartate into acetate and aspartic acid. In Canavan disease, spongiform encephalopathy of the brain causes progressive mental retardation, motor deficit and death. We have isolated a mouse with a novel ethylnitrosourea-induced mutation in Aspa. This mutant, named deaf14, carries a c.516T>A mutation that is predicted to cause a p.Y172X protein truncation. No full-length ASPA protein is produced in deaf14 brain and there is extensive spongy degeneration. Interestingly, we found that deaf14 mice have an attenuated startle in response to loud noise. The first auditory brainstem response peak has normal latency and amplitude but peaks II, III, IV and V have increased latency and decreased amplitude in deaf14 mice. Our work reveals a hitherto unappreciated pathology in a mouse model of Canavan disease, implying that auditory brainstem response testing could be used in diagnosis and to monitor the progression of this disease.",
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A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination. / Carpinelli, Marina R; Voss, Anne K; Manning, Michael G; Perera, Ashwyn A; Cooray, Anne A; Kile, Benjamin T; Burt, Rachel A.

In: Disease Models and Mechanisms, Vol. 7, No. 6, 2014, p. 649-657.

Research output: Contribution to journalArticleResearchpeer-review

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AU - Carpinelli, Marina R

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AB - Canavan disease is a leukodystrophy caused by mutations in the ASPA gene. This gene encodes the enzyme that converts N-acetylaspartate into acetate and aspartic acid. In Canavan disease, spongiform encephalopathy of the brain causes progressive mental retardation, motor deficit and death. We have isolated a mouse with a novel ethylnitrosourea-induced mutation in Aspa. This mutant, named deaf14, carries a c.516T>A mutation that is predicted to cause a p.Y172X protein truncation. No full-length ASPA protein is produced in deaf14 brain and there is extensive spongy degeneration. Interestingly, we found that deaf14 mice have an attenuated startle in response to loud noise. The first auditory brainstem response peak has normal latency and amplitude but peaks II, III, IV and V have increased latency and decreased amplitude in deaf14 mice. Our work reveals a hitherto unappreciated pathology in a mouse model of Canavan disease, implying that auditory brainstem response testing could be used in diagnosis and to monitor the progression of this disease.

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