2004 Fiscal Year Final Research Report Summary
Studies of Animal Development by Identification of Transcriptional Target Genes
Project/Area Number |
14380346
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Developmental biology
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Research Institution | The University of Tokyo (2003-2004) Nara Institute of Science and Technology (2002) |
Principal Investigator |
TAKAHASHI Naoki The University of Tokyo, Graduate School of Agricultural and Life Sciences, Professor, 大学院・農学生命科学研究科, 教授 (30179501)
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Project Period (FY) |
2002 – 2004
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Keywords | Transcriptional Regulation / Genome / Immunopurification / Gene Expression / Knockout Mice / Homeobox |
Research Abstract |
We have immunopurified the mouse mab-21 gene Mab2111 as a target candidate for HOXC4. The mab-21 gene was first identified because of its requirement for ray identity specification in Caenorhabditis elegans. It is now known to constitute a family of genes that are highly conserved from vertebrates to invertebrates, and two homologs, Mab2111 and Mab2112, have been identified in many species. We describe the generation of Mab2111-deficient mice with defects in eye and preputial gland formation. The mutant mouse eye has a rudimentary lens resulting from insufficient invagination of the lens placode caused by deficient proliferation. Chimera analyses suggest that the lens placode is affected in a cell-autonomous manner, although Mab2111 is expressed in both the lens placode and the optic vesicle. The defects in lens placode development correlate with delayed and insufficient expression of Foxe3, which is also required for lens development, while Maf, Sox2, Six3 and PAX6 levels are not significantly affected. Significant reduction of Mab2111 expression in the optic vesicle and overlying surface ectoderm in Sey homozygotes indicates that Mab2111 expression in the developing eye is dependent upon the functions of Pax6 gene products. We conclude that Mab2111 expression dependent on PAX6 is essential for lens placode growth and for formation of the lens vesicle ; lack of Mab2111 expression causes reduced expression of Foxe3 in a cell-autonomous manner.
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Research Products
(10 results)
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[Journal Article] PlexinA4 is necessary as a downstream target of Islet2 to mediate Slit signaling for promotion of sensory axon branching.2004
Author(s)
Miyashita, T., Yeo, S.-Y., Hirata, Y., Segawa, H., Wada, H., Little, M.H., Yamada, T., Takahashi, N., Okamoto, H.
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Journal Title
Development 131
Pages: 3705-3715
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Impaired motor coordination in mice lacking neural recognition molecule NB-3 of the contactin/F3 subgroup.2003
Author(s)
Takeda, Y., Akasaka, K., Lee, S., Kobayashi, S., Kawano, H., Murayama, S., Takahashi.N..Hashimoto, K., Kano, M., Asano, M., Sudo, K., Iwakura, Y., Watanabe, K.
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Journal Title
J. Neurobiology 56
Pages: 252-265
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Cell-autonomous involvement of Mab2111 is essential for lens placode development.2003
Author(s)
Yamada, R., Mizutani-Koseki, Y., Hasegawa, T., Ohsumi, N., Koseki, H., Takahashi, N.
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Journal Title
Development 130
Pages: 1759-1770
Description
「研究成果報告書概要(欧文)」より
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