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Midline Signaling in the Primordium of the Zebrafish Anterior Central Nervous System
In all vertebrates the brain develops from the enlarged anterior part of the neural plate. However, in the zebrafish mutant cyclops, the girth of the central nervous system (CNS) is nearly uniform along its length. Changes in expression patterns of homeobox genes and neuronal markers reveal a massiv...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1994-03, Vol.91 (6), p.2061-2065 |
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container_end_page | 2065 |
container_issue | 6 |
container_start_page | 2061 |
container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Hatta, Kohei Puschel, Andreas W. Kimmel, Charles B. |
description | In all vertebrates the brain develops from the enlarged anterior part of the neural plate. However, in the zebrafish mutant cyclops, the girth of the central nervous system (CNS) is nearly uniform along its length. Changes in expression patterns of homeobox genes and neuronal markers reveal a massive deletion of the ventral forebrain, particularly the diencephalon, as well as its precursor region in the neural plate. The deletion is due to a nonautonomous action of the mutation: very few wild-type cells transplanted to the midline of a mutant embryo can rescue the forebrain phenotype, including cyclopia. Establishment of forebrain ventral positional coordinates may thus require inductive signaling by forebrain midline cells whose specification depends upon the cyclops gene product. |
doi_str_mv | 10.1073/pnas.91.6.2061 |
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However, in the zebrafish mutant cyclops, the girth of the central nervous system (CNS) is nearly uniform along its length. Changes in expression patterns of homeobox genes and neuronal markers reveal a massive deletion of the ventral forebrain, particularly the diencephalon, as well as its precursor region in the neural plate. The deletion is due to a nonautonomous action of the mutation: very few wild-type cells transplanted to the midline of a mutant embryo can rescue the forebrain phenotype, including cyclopia. 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However, in the zebrafish mutant cyclops, the girth of the central nervous system (CNS) is nearly uniform along its length. Changes in expression patterns of homeobox genes and neuronal markers reveal a massive deletion of the ventral forebrain, particularly the diencephalon, as well as its precursor region in the neural plate. The deletion is due to a nonautonomous action of the mutation: very few wild-type cells transplanted to the midline of a mutant embryo can rescue the forebrain phenotype, including cyclopia. Establishment of forebrain ventral positional coordinates may thus require inductive signaling by forebrain midline cells whose specification depends upon the cyclops gene product.</description><subject>Animals</subject><subject>Biology</subject><subject>Cell transplantation</subject><subject>Central nervous system</subject><subject>Central Nervous System - embryology</subject><subject>Central Nervous System - physiology</subject><subject>Cyclopes</subject><subject>Danio rerio</subject><subject>Diencephalon</subject><subject>Embryo, Nonmammalian</subject><subject>Embryos</subject><subject>Fish</subject><subject>Forebrain</subject><subject>Freshwater</subject><subject>Genes, Homeobox</subject><subject>Midbrain</subject><subject>Mosaic</subject><subject>Nervous system</subject><subject>Neurons</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Prosencephalon - embryology</subject><subject>Prosencephalon - physiology</subject><subject>Prosencephalon - transplantation</subject><subject>Signal Transduction</subject><subject>Zebrafish</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNqFkc2L1DAYxoMo67h69aQQPOyt9c1Hkwa8LIOrwvoBu168hLRNZzK0zZiki_vfm3HGYRTBU0Ke3_PyvHkQek6gJCDZ6-1kYqlIKUoKgjxACwKKFIIreIgWAFQWNaf8MXoS4wYAVFXDGTqTCqRUdIFuP7pucJPFN241mXxbYTfhtLb4S3CjD52bR-z7Xy_fbBNM7-IaX07JBucDXtopBTPgTzbc-Tnim_uY7PgUPerNEO2zw3mOvl69vV2-L64_v_uwvLwu2qomqSB9R3sq2sYSxqQSjaCdZDWHumOmUV1PFWuVrSQlkleSg-wYMKsMb1pmK8PO0Zv93O3cjLZr92H0Nic34V574_SfyuTWeuXvNGcMVLZfHOzBf59tTHp0sbXDYCabl9FScCCM8_-CRCgBTIoMvvoL3Pg55H-NmuZRhLO6ylC5h9rgYwy2PwYmoHed6l2nWhEt9K7TbHh5uuYRP5R4Em_n-60e_bqfhyHZH-lk0D_BrL_Y65uYfDgClAlOJGU_ATrCvmA</recordid><startdate>19940315</startdate><enddate>19940315</enddate><creator>Hatta, Kohei</creator><creator>Puschel, Andreas W.</creator><creator>Kimmel, Charles B.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19940315</creationdate><title>Midline Signaling in the Primordium of the Zebrafish Anterior Central Nervous System</title><author>Hatta, Kohei ; 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source | JSTOR Archival Journals and Primary Sources Collection; PMC |
subjects | Animals Biology Cell transplantation Central nervous system Central Nervous System - embryology Central Nervous System - physiology Cyclopes Danio rerio Diencephalon Embryo, Nonmammalian Embryos Fish Forebrain Freshwater Genes, Homeobox Midbrain Mosaic Nervous system Neurons Phenotype Phenotypes Prosencephalon - embryology Prosencephalon - physiology Prosencephalon - transplantation Signal Transduction Zebrafish |
title | Midline Signaling in the Primordium of the Zebrafish Anterior Central Nervous System |
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