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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 |
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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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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.</description><identifier>ISSN: 0192-253X</identifier><identifier>EISSN: 1520-6408</identifier><identifier>DOI: 10.1002/(SICI)1520-6408(1998)23:4<299::AID-DVG5>3.0.CO;2-G</identifier><identifier>PMID: 9883582</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>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</subject><ispartof>Developmental genetics, 1998, Vol.23 (4), p.299-316</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9883582$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grimm, Christina</creatorcontrib><creatorcontrib>Chatterjee, Bimal</creatorcontrib><creatorcontrib>Favor, Jack</creatorcontrib><creatorcontrib>Immervoll, Thomas</creatorcontrib><creatorcontrib>Löster, Jana</creatorcontrib><creatorcontrib>Klopp, Norman</creatorcontrib><creatorcontrib>Sandulache, Rodica</creatorcontrib><creatorcontrib>Graw, Jochen</creatorcontrib><title>Aphakia (ak), a mouse mutation affecting early eye development: Fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern</title><title>Developmental genetics</title><addtitle>Dev. 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. 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.</description><subject>Animals</subject><subject>Chromosome Mapping</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Eye - embryology</subject><subject>eye development</subject><subject>Eye Proteins - genetics</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Homeobox Protein SIX3</subject><subject>Homeodomain Proteins - genetics</subject><subject>linkage analysis</subject><subject>Mice</subject><subject>Mice, Mutant Strains</subject><subject>mouse mutant</subject><subject>Mutation</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Paired Box Transcription Factors</subject><subject>Pax2</subject><subject>Pax6</subject><subject>PAX6 Transcription Factor</subject><subject>Repressor Proteins</subject><subject>Six3</subject><subject>Six3, α‐crystallin</subject><subject>α-crystallin</subject><issn>0192-253X</issn><issn>1520-6408</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkcuO0zAUhiMEGsrAIyB5hVppUnyJk7ggpCpDQ6VCgQFmdkdOcjJjmhtJCu3b8Kg4bdUt8sKy_-_8i_M5zozRKaOUvx7fLKPlhElOXd-j4ZgpFU64mHlvuVKz2Xx57V7_iOU7MaXTaP2Gu_EjZ3TGHzsjyhR3uRR3T51nXfeTUqp8T144FyoMhQz5yPk7bx70xmgy1pvJFdGkrLcdknLb697UFdF5jmlvqnuCui32BPdIMvyNRd2UWPUzsjCVxXXTWOaKpHXVmQzb43Cdk1RXmcl0j-QeK-yIfRJd9NhiRj7rnX_4uDE7ccgJ7poWu24YbnRvseq58yTXRYcvTvel833x_lv0wV2t42U0X7mG-1K6fsKp4JJhkCUyp2HIKfNlyiVNVEL9VMpcp2GWoKezwEuUp6Rn0ZSnHL088MWl8-rY27T1ry12PZSmS7EodIV2JeArJpjP_g-ywB7OlAVfnsBtUmIGTWtK3e7htHubfz3mf0yB-3PMKAzyYXAPg0wYZMLgHrgAD6x7sOphUA8CKERr4BAf3rbUPZaarsfduVS3G_ADEUi4_RTDx8UqEuzuFr6If-iBtwU</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Grimm, Christina</creator><creator>Chatterjee, Bimal</creator><creator>Favor, Jack</creator><creator>Immervoll, Thomas</creator><creator>Löster, Jana</creator><creator>Klopp, Norman</creator><creator>Sandulache, Rodica</creator><creator>Graw, Jochen</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>1998</creationdate><title>Aphakia (ak), a mouse mutation affecting early eye development: Fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern</title><author>Grimm, Christina ; Chatterjee, Bimal ; Favor, Jack ; Immervoll, Thomas ; Löster, Jana ; Klopp, Norman ; Sandulache, Rodica ; Graw, Jochen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2655-6b203251e7db5f08820165c250b9b06c55fac8dbe4ad74b949547dbc2c2e4f763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Chromosome Mapping</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Eye - embryology</topic><topic>eye development</topic><topic>Eye Proteins - genetics</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Homeobox Protein SIX3</topic><topic>Homeodomain Proteins - genetics</topic><topic>linkage analysis</topic><topic>Mice</topic><topic>Mice, Mutant Strains</topic><topic>mouse mutant</topic><topic>Mutation</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Paired Box Transcription Factors</topic><topic>Pax2</topic><topic>Pax6</topic><topic>PAX6 Transcription Factor</topic><topic>Repressor Proteins</topic><topic>Six3</topic><topic>Six3, α‐crystallin</topic><topic>α-crystallin</topic><toplevel>online_resources</toplevel><creatorcontrib>Grimm, Christina</creatorcontrib><creatorcontrib>Chatterjee, Bimal</creatorcontrib><creatorcontrib>Favor, Jack</creatorcontrib><creatorcontrib>Immervoll, Thomas</creatorcontrib><creatorcontrib>Löster, Jana</creatorcontrib><creatorcontrib>Klopp, Norman</creatorcontrib><creatorcontrib>Sandulache, Rodica</creatorcontrib><creatorcontrib>Graw, Jochen</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grimm, Christina</au><au>Chatterjee, Bimal</au><au>Favor, Jack</au><au>Immervoll, Thomas</au><au>Löster, Jana</au><au>Klopp, Norman</au><au>Sandulache, Rodica</au><au>Graw, Jochen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aphakia (ak), a mouse mutation affecting early eye development: Fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern</atitle><jtitle>Developmental genetics</jtitle><addtitle>Dev. Genet</addtitle><date>1998</date><risdate>1998</risdate><volume>23</volume><issue>4</issue><spage>299</spage><epage>316</epage><pages>299-316</pages><issn>0192-253X</issn><eissn>1520-6408</eissn><abstract>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.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9883582</pmid><doi>10.1002/(SICI)1520-6408(1998)23:4<299::AID-DVG5>3.0.CO;2-G</doi><tpages>18</tpages></addata></record> |
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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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