Medical Journals

Temporal and Spatial Expression Profiles of the Fat3 Protein, a Giant Cadherin Molecule, During Mouse Development.

Authors:
  • Nagae Shigenori
  • Tanoue Takuji
  • Takeichi Masatoshi

From: Graduate School of Biostudies, Kyoto University, Kyoto, Japan.

Developmental dynamics : an official publication of the American Association of Anatomists

  • Publish Date: Feb 2007
  • ISSN: 1058-8388
  • Volume: 236
  • Issue: 2
  • Pages: 534-43
  • Medium: Print
  • Language: English
  • Citation (JAMA): Nagae Shigenori, Tanoue Takuji, Takeichi Masatoshi, et al. Temporal and Spatial Expression Profiles of the Fat3 Protein, a Giant Cadherin Molecule, During Mouse Development.. Dev. Dyn. Feb 2007;236:534-43

Abstract

Cadherins constitute a superfamily of cell-cell interaction molecules that participate in morphogenetic processes of animal development. Fat cadherins are the largest members of this superfamily, with 34 extracellular cadherin repeats. Classic Fat, identified in Drosophila, is known to regulate cell proliferation and planar cell polarity. Although 4 subtypes of Fat cadherin, Fat1, Fat2, Fat3, and Fat4/Fat-J, have been identified in vertebrates, their protein localization remains largely unknown. Here we describe the mRNA and protein distributions of Fat3 during mouse development. We found that Fat3 expression was restricted to the nervous system. In the brain, Fat3 was expressed in a variety of regions and axon fascicles. However, its strongest expression was observed in the olfactory bulb and retina. Detailed analysis of Fat3 in the developing olfactory bulb revealed that Fat3 mRNA was mainly expressed by mitral cells and that its proteins were densely localized along the dendrites of these cells as well as in their axons to some extent. Fat3 transcripts in the retina were expressed by amacrine and ganglion cells, and its proteins were concentrated in the inner plexiform layer throughout development. Based on these observations, we suggest that Fat3 plays a role in the interactions between neurites derived from specific subsets of neurons during development.

Mesh Headings (Keywords): Animals, Blotting, Western, Cadherins, DNA Primers, Embryonic Development, Gene Expression Profiling, Immunohistochemistry, In Situ Hybridization, Mice


Check for Full Text / PubMed Unique Identifier (PMID): 17131403


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.