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The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants

There are three known splice variants of Type Iγ phosphatidylinositol 4-phosphate 5-kinase (PIPkin Iγ): PIPkins Iγ87, Iγ90, and the most recently cloned (Giudici, M.L., Emson, P.C. and Irvine, R.F. (2004) A novel neuronal-specific splice variant of Type I phosphatidylinositol 4-phosphate 5-kinase is...

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Detalles Bibliográficos
Autores principales: Giudici, Maria-Luisa, Lee, Koon, Lim, Rongxuan, Irvine, Robin F.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1839758/
https://www.ncbi.nlm.nih.gov/pubmed/17157843
http://dx.doi.org/10.1016/j.febslet.2006.11.052
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author Giudici, Maria-Luisa
Lee, Koon
Lim, Rongxuan
Irvine, Robin F.
author_facet Giudici, Maria-Luisa
Lee, Koon
Lim, Rongxuan
Irvine, Robin F.
author_sort Giudici, Maria-Luisa
collection PubMed
description There are three known splice variants of Type Iγ phosphatidylinositol 4-phosphate 5-kinase (PIPkin Iγ): PIPkins Iγ87, Iγ90, and the most recently cloned (Giudici, M.L., Emson, P.C. and Irvine, R.F. (2004) A novel neuronal-specific splice variant of Type I phosphatidylinositol 4-phosphate 5-kinase isoform gamma. Biochem. J. 379, 489–496) PIPkin IγC (here called PIPkin Iγ93). Here, we have explored the subcellular localisation and mobility of Type I PIPkins in transfected cells by confocal microscopy and flourescence recovery after photobleaching. The unique behaviour shown by PIPkin Iγ93 is consistent with its suggested distinct function. Moreover, the markedly different localisation and mobility of active versus inactive PIPkin Iγ93 provide insights into the factors that dictate cellular targeting of Type Iγ PIPkins.
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spelling pubmed-18397582007-06-22 The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants Giudici, Maria-Luisa Lee, Koon Lim, Rongxuan Irvine, Robin F. FEBS Lett Article There are three known splice variants of Type Iγ phosphatidylinositol 4-phosphate 5-kinase (PIPkin Iγ): PIPkins Iγ87, Iγ90, and the most recently cloned (Giudici, M.L., Emson, P.C. and Irvine, R.F. (2004) A novel neuronal-specific splice variant of Type I phosphatidylinositol 4-phosphate 5-kinase isoform gamma. Biochem. J. 379, 489–496) PIPkin IγC (here called PIPkin Iγ93). Here, we have explored the subcellular localisation and mobility of Type I PIPkins in transfected cells by confocal microscopy and flourescence recovery after photobleaching. The unique behaviour shown by PIPkin Iγ93 is consistent with its suggested distinct function. Moreover, the markedly different localisation and mobility of active versus inactive PIPkin Iγ93 provide insights into the factors that dictate cellular targeting of Type Iγ PIPkins. Elsevier Science B.V 2006-12-22 /pmc/articles/PMC1839758/ /pubmed/17157843 http://dx.doi.org/10.1016/j.febslet.2006.11.052 Text en © 2006 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Giudici, Maria-Luisa
Lee, Koon
Lim, Rongxuan
Irvine, Robin F.
The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants
title The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants
title_full The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants
title_fullStr The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants
title_full_unstemmed The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants
title_short The intracellular localisation and mobility of Type Iγ phosphatidylinositol 4P 5-kinase splice variants
title_sort intracellular localisation and mobility of type iγ phosphatidylinositol 4p 5-kinase splice variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1839758/
https://www.ncbi.nlm.nih.gov/pubmed/17157843
http://dx.doi.org/10.1016/j.febslet.2006.11.052
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