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The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth

Fibroblast growth factor (Fgf) signalling plays a crucial role in many developmental processes. Among the Fgf pathway ligands, Fgf9 (UniProt: P54130) has been demonstrated to participate in maturation of various organs and tissues including skeleton, testes, lung, heart, and eye. Here we establish a...

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Autores principales: Puk, Oliver, Möller, Gabriele, Geerlof, Arie, Krowiorz, Kathrin, Ahmad, Nafees, Wagner, Sibylle, Adamski, Jerzy, de Angelis, Martin Hrabé, Graw, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157460/
https://www.ncbi.nlm.nih.gov/pubmed/21858205
http://dx.doi.org/10.1371/journal.pone.0023678
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author Puk, Oliver
Möller, Gabriele
Geerlof, Arie
Krowiorz, Kathrin
Ahmad, Nafees
Wagner, Sibylle
Adamski, Jerzy
de Angelis, Martin Hrabé
Graw, Jochen
author_facet Puk, Oliver
Möller, Gabriele
Geerlof, Arie
Krowiorz, Kathrin
Ahmad, Nafees
Wagner, Sibylle
Adamski, Jerzy
de Angelis, Martin Hrabé
Graw, Jochen
author_sort Puk, Oliver
collection PubMed
description Fibroblast growth factor (Fgf) signalling plays a crucial role in many developmental processes. Among the Fgf pathway ligands, Fgf9 (UniProt: P54130) has been demonstrated to participate in maturation of various organs and tissues including skeleton, testes, lung, heart, and eye. Here we establish a novel Fgf9 allele, discovered in a dominant N-ethyl-N-nitrosourea (ENU) screen for eye-size abnormalities using the optical low coherence interferometry technique. The underlying mouse mutant line Aca12 was originally identified because of its significantly reduced lens thickness. Linkage studies located Aca12 to chromosome 14 within a 3.6 Mb spanning interval containing the positional candidate genes Fgf9 (MGI: 104723), Gja3 (MGI: 95714), and Ift88 (MGI: 98715). While no sequence differences were found in Gja3 and Ift88, we identified an A→G missense mutation at cDNA position 770 of the Fgf9 gene leading to an Y162C amino acid exchange. In contrast to previously described Fgf9 mutants, Fgf9(Y162C) carriers were fully viable and did not reveal reduced body-size, male-to-female sexual reversal or skeletal malformations. The histological analysis of the retina as well as its basic functional characterization by electroretinography (ERG) did not show any abnormality. However, the analysis of head-tracking response of the Fgf9(Y162C) mutants in a virtual drum indicated a gene-dosage dependent vision loss of almost 50%. The smaller lenses in Fgf9(Y162C) suggested a role of Fgf9 during lens development. Histological investigations showed that lens growth retardation starts during embryogenesis and continues after birth. Young Fgf9(Y162C) lenses remained transparent but developed age-related cataracts. Taken together, Fgf9(Y162C) is a novel neomorphic allele that initiates microphakia and reduced vision without effects on organs and tissues outside the eye. Our data point to a role of Fgf9 signalling in primary and secondary lens fiber cell growth. The results underline the importance of allelic series to fully understand multiple functions of a gene.
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spelling pubmed-31574602011-08-19 The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth Puk, Oliver Möller, Gabriele Geerlof, Arie Krowiorz, Kathrin Ahmad, Nafees Wagner, Sibylle Adamski, Jerzy de Angelis, Martin Hrabé Graw, Jochen PLoS One Research Article Fibroblast growth factor (Fgf) signalling plays a crucial role in many developmental processes. Among the Fgf pathway ligands, Fgf9 (UniProt: P54130) has been demonstrated to participate in maturation of various organs and tissues including skeleton, testes, lung, heart, and eye. Here we establish a novel Fgf9 allele, discovered in a dominant N-ethyl-N-nitrosourea (ENU) screen for eye-size abnormalities using the optical low coherence interferometry technique. The underlying mouse mutant line Aca12 was originally identified because of its significantly reduced lens thickness. Linkage studies located Aca12 to chromosome 14 within a 3.6 Mb spanning interval containing the positional candidate genes Fgf9 (MGI: 104723), Gja3 (MGI: 95714), and Ift88 (MGI: 98715). While no sequence differences were found in Gja3 and Ift88, we identified an A→G missense mutation at cDNA position 770 of the Fgf9 gene leading to an Y162C amino acid exchange. In contrast to previously described Fgf9 mutants, Fgf9(Y162C) carriers were fully viable and did not reveal reduced body-size, male-to-female sexual reversal or skeletal malformations. The histological analysis of the retina as well as its basic functional characterization by electroretinography (ERG) did not show any abnormality. However, the analysis of head-tracking response of the Fgf9(Y162C) mutants in a virtual drum indicated a gene-dosage dependent vision loss of almost 50%. The smaller lenses in Fgf9(Y162C) suggested a role of Fgf9 during lens development. Histological investigations showed that lens growth retardation starts during embryogenesis and continues after birth. Young Fgf9(Y162C) lenses remained transparent but developed age-related cataracts. Taken together, Fgf9(Y162C) is a novel neomorphic allele that initiates microphakia and reduced vision without effects on organs and tissues outside the eye. Our data point to a role of Fgf9 signalling in primary and secondary lens fiber cell growth. The results underline the importance of allelic series to fully understand multiple functions of a gene. Public Library of Science 2011-08-17 /pmc/articles/PMC3157460/ /pubmed/21858205 http://dx.doi.org/10.1371/journal.pone.0023678 Text en Puk et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Puk, Oliver
Möller, Gabriele
Geerlof, Arie
Krowiorz, Kathrin
Ahmad, Nafees
Wagner, Sibylle
Adamski, Jerzy
de Angelis, Martin Hrabé
Graw, Jochen
The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth
title The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth
title_full The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth
title_fullStr The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth
title_full_unstemmed The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth
title_short The Pathologic Effect of a Novel Neomorphic Fgf9(Y162C) Allele Is Restricted to Decreased Vision and Retarded Lens Growth
title_sort pathologic effect of a novel neomorphic fgf9(y162c) allele is restricted to decreased vision and retarded lens growth
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157460/
https://www.ncbi.nlm.nih.gov/pubmed/21858205
http://dx.doi.org/10.1371/journal.pone.0023678
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