Literature DB >> 20875818

ankAT-1 is a novel gene mediating the apical tuft formation in the sea urchin embryo.

Shunsuke Yaguchi1, Junko Yaguchi, Zheng Wei, Kogiku Shiba, Lynne M Angerer, Kazuo Inaba.   

Abstract

In sea urchin embryos, the apical tuft forms within the neurogenic animal plate. When FoxQ2, one of the earliest factors expressed specifically in the animal plate by early blastula stage, is knocked down, the structure of the apical tuft is altered. To determine the basis of this phenotype, we identified FoxQ2-dependent genes using microarray analysis. The most strongly down-regulated gene in FoxQ2 morphants encodes a protein with ankyrin repeats region in its N-terminal domain. We named this gene ankAT-1, Ankyrin-containing gene specific for Apical Tuft. Initially its expression in the animal pole region of very early blastula stage embryos is FoxQ2-independent but becomes FoxQ2-dependent beginning at mesenchyme blastula stage and continuing in the animal plate of 3-day larvae. Furthermore, like FoxQ2, this gene is expressed throughout the expanded apical tuft region that forms in embryos lacking nuclear β-catenin. When AnkAT-1 is knocked-down by injecting a morpholino, the cilia at the animal plate in the resulting embryos are much shorter and their motility is less than that of motile cilia in other ectoderm cells, and remains similar to that of long apical tuft cilia. We conclude that AnkAT-1 is involved in regulating the length of apical tuft cilia.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20875818      PMCID: PMC2976814          DOI: 10.1016/j.ydbio.2010.09.011

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  43 in total

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Authors:  Carter M Takacs; Gabriele Amore; Paola Oliveri; Albert J Poustka; Diana Wang; Robert D Burke; Kevin J Peterson
Journal:  Dev Biol       Date:  2004-05-01       Impact factor: 3.582

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Authors:  R L Morris; J M Scholey
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  15 in total

1.  Fez function is required to maintain the size of the animal plate in the sea urchin embryo.

Authors:  Shunsuke Yaguchi; Junko Yaguchi; Zheng Wei; Yinhua Jin; Lynne M Angerer; Kazuo Inaba
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Review 2.  The evolution of nervous system patterning: insights from sea urchin development.

Authors:  Lynne M Angerer; Shunsuke Yaguchi; Robert C Angerer; Robert D Burke
Journal:  Development       Date:  2011-09       Impact factor: 6.868

3.  Evolution of nitric oxide regulation of gut function.

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Journal:  Proc Natl Acad Sci U S A       Date:  2019-03-04       Impact factor: 11.205

4.  Zinc finger homeobox is required for the differentiation of serotonergic neurons in the sea urchin embryo.

Authors:  Junko Yaguchi; Lynne M Angerer; Kazuo Inaba; Shunsuke Yaguchi
Journal:  Dev Biol       Date:  2011-12-22       Impact factor: 3.582

5.  An anterior signaling center patterns and sizes the anterior neuroectoderm of the sea urchin embryo.

Authors:  Ryan C Range; Zheng Wei
Journal:  Development       Date:  2016-03-07       Impact factor: 6.868

6.  A single cell RNA sequencing resource for early sea urchin development.

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7.  Development of the larval anterior neurogenic domains of Terebratalia transversa (Brachiopoda) provides insights into the diversification of larval apical organs and the spiralian nervous system.

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8.  The Fox/Forkhead transcription factor family of the hemichordate Saccoglossus kowalevskii.

Authors:  Jens H Fritzenwanker; John Gerhart; Robert M Freeman; Christopher J Lowe
Journal:  Evodevo       Date:  2014-05-07       Impact factor: 2.250

9.  Glutathione transferase theta in apical ciliary tuft regulates mechanical reception and swimming behavior of Sea Urchin Embryos.

Authors:  Yinhua Jin; Shunsuke Yaguchi; Kogiku Shiba; Lixy Yamada; Junko Yaguchi; Daisuke Shibata; Hitoshi Sawada; Kazuo Inaba
Journal:  Cytoskeleton (Hoboken)       Date:  2013-08-19

10.  bicaudal-C is required for the formation of anterior neurogenic ectoderm in the sea urchin embryo.

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