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Aphakia (ak), a mouse mutation affecting early eye development: Fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern

The homozygous mouse mutant aphakia (ak) has been characterized by bilaterally aphakic eyes without a pupil [Varnum DS, Stevens, LC (1968): J Hered 59:147–150]. The mutation was mapped to chromosome 19 [Varnum DS, Stevens, LC (1975): Mouse News Lett 53:35]. Our linkage studies yielded a precise loca...

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Published in:Developmental genetics 1998, Vol.23 (4), p.299-316
Main Authors: Grimm, Christina, Chatterjee, Bimal, Favor, Jack, Immervoll, Thomas, Löster, Jana, Klopp, Norman, Sandulache, Rodica, Graw, Jochen
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container_title Developmental genetics
container_volume 23
creator Grimm, Christina
Chatterjee, Bimal
Favor, Jack
Immervoll, Thomas
Löster, Jana
Klopp, Norman
Sandulache, Rodica
Graw, Jochen
description The homozygous mouse mutant aphakia (ak) has been characterized by bilaterally aphakic eyes without a pupil [Varnum DS, Stevens, LC (1968): J Hered 59:147–150]. The mutation was mapped to chromosome 19 [Varnum DS, Stevens, LC (1975): Mouse News Lett 53:35]. Our linkage studies yielded a precise localization of the ak gene 0.6 ± 0.3 cM proximal to the microsatellite marker D19Mit10 and 0.7 ± 0.4 cM distal to D19Mit4 and D19Mit91. No recombination was found with the marker D19Mit9 among 418 backcross offspring tested. The developmental control gene Pax2 mapped 11.0 ± 3.5 cM proximal to ak and is excluded as a candidate gene. Sequence analysis of Fgf8 and Chuk1, which are localized close to the marker D19Mit10, detected no mutations in the ak/ak mutants. Histological analysis of homozygous mutants suggested the arrest of lens development at the lens stalk stage, a transient morphological structure during the formation of the lens vesicle. In the lens remnants, Pax6 and Six3 are expressed, whereas in the persisting lens stalk only Pax6 was detected. The expression pattern of Pax2 appeared normal; Cryaa expression could not be detected. As a consequence of the arrested lens development, other ocular tissues that require for their development information from the intact lens, such as iris, ciliary muscle, retina, and vitreous body, are absent or formed abnormally. Dev. Genet. 23:299–316, 1998. © 1998 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1520-6408(1998)23:4<299::AID-DVG5>3.0.CO;2-G
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Genet</addtitle><description>The homozygous mouse mutant aphakia (ak) has been characterized by bilaterally aphakic eyes without a pupil [Varnum DS, Stevens, LC (1968): J Hered 59:147–150]. The mutation was mapped to chromosome 19 [Varnum DS, Stevens, LC (1975): Mouse News Lett 53:35]. Our linkage studies yielded a precise localization of the ak gene 0.6 ± 0.3 cM proximal to the microsatellite marker D19Mit10 and 0.7 ± 0.4 cM distal to D19Mit4 and D19Mit91. No recombination was found with the marker D19Mit9 among 418 backcross offspring tested. The developmental control gene Pax2 mapped 11.0 ± 3.5 cM proximal to ak and is excluded as a candidate gene. Sequence analysis of Fgf8 and Chuk1, which are localized close to the marker D19Mit10, detected no mutations in the ak/ak mutants. Histological analysis of homozygous mutants suggested the arrest of lens development at the lens stalk stage, a transient morphological structure during the formation of the lens vesicle. 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ispartof Developmental genetics, 1998, Vol.23 (4), p.299-316
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1520-6408
language eng
recordid cdi_proquest_miscellaneous_69131616
source Wiley-Blackwell Read & Publish Collection
subjects Animals
Chromosome Mapping
DNA-Binding Proteins - genetics
Eye - embryology
eye development
Eye Proteins - genetics
Gene Expression Regulation, Developmental
Homeobox Protein SIX3
Homeodomain Proteins - genetics
linkage analysis
Mice
Mice, Mutant Strains
mouse mutant
Mutation
Nerve Tissue Proteins - genetics
Paired Box Transcription Factors
Pax2
Pax6
PAX6 Transcription Factor
Repressor Proteins
Six3
Six3, α‐crystallin
α-crystallin
title Aphakia (ak), a mouse mutation affecting early eye development: Fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern
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