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Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene

The existence of a neurofilament-deficient mutant of Japanese quail was recently documented (Yamasaki, H., C. Itakura, and M. Mizutani. 1991. Acta Neuropathol. 82:427-434), but the genetic events leading to the neurofilament deficiency have yet to be determined. Our molecular biological analyses rev...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1993
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2200107/
https://www.ncbi.nlm.nih.gov/pubmed/8468353
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description The existence of a neurofilament-deficient mutant of Japanese quail was recently documented (Yamasaki, H., C. Itakura, and M. Mizutani. 1991. Acta Neuropathol. 82:427-434), but the genetic events leading to the neurofilament deficiency have yet to be determined. Our molecular biological analyses revealed that the expression of neurofilament-L (NF- L) gene was specifically repressed in neurons of this mutant. To search for mutation(s) responsible for the shutdown of this gene expression, we cloned and sequenced the NF-L genes in the wild-type and mutant quails. It is eventually found that the NF-L gene in the mutant includes a nonsense mutation at the deduced amino acid residue 114, indicating that the mutant is incapable of producing even a trace amount of polymerization-competent NF-L protein at any situation. The identification of this nonsense mutation provides us with a solid basis on which molecular mechanisms underlying the alteration in the neuronal cytoskeletal architecture in the mutant should be interpreted.
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spelling pubmed-22001072008-05-01 Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene J Cell Biol Articles The existence of a neurofilament-deficient mutant of Japanese quail was recently documented (Yamasaki, H., C. Itakura, and M. Mizutani. 1991. Acta Neuropathol. 82:427-434), but the genetic events leading to the neurofilament deficiency have yet to be determined. Our molecular biological analyses revealed that the expression of neurofilament-L (NF- L) gene was specifically repressed in neurons of this mutant. To search for mutation(s) responsible for the shutdown of this gene expression, we cloned and sequenced the NF-L genes in the wild-type and mutant quails. It is eventually found that the NF-L gene in the mutant includes a nonsense mutation at the deduced amino acid residue 114, indicating that the mutant is incapable of producing even a trace amount of polymerization-competent NF-L protein at any situation. The identification of this nonsense mutation provides us with a solid basis on which molecular mechanisms underlying the alteration in the neuronal cytoskeletal architecture in the mutant should be interpreted. The Rockefeller University Press 1993-04-02 /pmc/articles/PMC2200107/ /pubmed/8468353 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
title Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
title_full Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
title_fullStr Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
title_full_unstemmed Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
title_short Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene
title_sort neurofilament deficiency in quail caused by nonsense mutation in neurofilament-l gene
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2200107/
https://www.ncbi.nlm.nih.gov/pubmed/8468353