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Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile
Shrew-1, also called AJAP1, is a transmembrane protein associated with E-cadherin-mediated adherence junctions and a putative tumor suppressor. Apart from its interaction with β-catenin and involvement in E-cadherin internalization, little structure or function information exists. Here we explored s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155531/ https://www.ncbi.nlm.nih.gov/pubmed/27870635 http://dx.doi.org/10.1242/bio.019463 |
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author | Klemmt, Petra A. B. Resch, Eduard Smyrek, Isabell Engels, Knut Stelzer, Ernst H. K. Starzinski-Powitz, Anna |
author_facet | Klemmt, Petra A. B. Resch, Eduard Smyrek, Isabell Engels, Knut Stelzer, Ernst H. K. Starzinski-Powitz, Anna |
author_sort | Klemmt, Petra A. B. |
collection | PubMed |
description | Shrew-1, also called AJAP1, is a transmembrane protein associated with E-cadherin-mediated adherence junctions and a putative tumor suppressor. Apart from its interaction with β-catenin and involvement in E-cadherin internalization, little structure or function information exists. Here we explored shrew-1 expression during postnatal differentiation of mammary gland as a model system. Immunohistological analyses with antibodies against either the extracellular or the cytoplasmic domains of shrew-1 consistently revealed the expression of full-length shrew-1 in myoepithelial cells, but only part of it in luminal cells. While shrew-1 localization remained unaltered in myoepithelial cells, nuclear localization occurred in luminal cells during lactation. Based on these observations, we identified two unknown shrew-1 transcript variants encoding N-terminally truncated proteins. The smallest shrew-1 protein lacks the extracellular domain and is most likely the only variant present in luminal cells. RNA analyses of human tissues confirmed that the novel transcript variants of shrew-1 exist in vivo and exhibit a differential tissue expression profile. We conclude that our findings are essential for the understanding and interpretation of future functional and interactome analyses of shrew-1 variants. |
format | Online Article Text |
id | pubmed-5155531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51555312016-12-16 Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile Klemmt, Petra A. B. Resch, Eduard Smyrek, Isabell Engels, Knut Stelzer, Ernst H. K. Starzinski-Powitz, Anna Biol Open Research Article Shrew-1, also called AJAP1, is a transmembrane protein associated with E-cadherin-mediated adherence junctions and a putative tumor suppressor. Apart from its interaction with β-catenin and involvement in E-cadherin internalization, little structure or function information exists. Here we explored shrew-1 expression during postnatal differentiation of mammary gland as a model system. Immunohistological analyses with antibodies against either the extracellular or the cytoplasmic domains of shrew-1 consistently revealed the expression of full-length shrew-1 in myoepithelial cells, but only part of it in luminal cells. While shrew-1 localization remained unaltered in myoepithelial cells, nuclear localization occurred in luminal cells during lactation. Based on these observations, we identified two unknown shrew-1 transcript variants encoding N-terminally truncated proteins. The smallest shrew-1 protein lacks the extracellular domain and is most likely the only variant present in luminal cells. RNA analyses of human tissues confirmed that the novel transcript variants of shrew-1 exist in vivo and exhibit a differential tissue expression profile. We conclude that our findings are essential for the understanding and interpretation of future functional and interactome analyses of shrew-1 variants. The Company of Biologists Ltd 2016-11-15 /pmc/articles/PMC5155531/ /pubmed/27870635 http://dx.doi.org/10.1242/bio.019463 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Klemmt, Petra A. B. Resch, Eduard Smyrek, Isabell Engels, Knut Stelzer, Ernst H. K. Starzinski-Powitz, Anna Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile |
title | Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile |
title_full | Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile |
title_fullStr | Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile |
title_full_unstemmed | Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile |
title_short | Alternative exon usage creates novel transcript variants of tumor suppressor SHREW-1 gene with differential tissue expression profile |
title_sort | alternative exon usage creates novel transcript variants of tumor suppressor shrew-1 gene with differential tissue expression profile |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155531/ https://www.ncbi.nlm.nih.gov/pubmed/27870635 http://dx.doi.org/10.1242/bio.019463 |
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