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Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin

TGN38 and TGN41 are isoforms of a monotopic integral membrane protein which recycles between the trans Golgi network (TGN) and the cell surface, but which, at steady state, is predominantly located in the TGN. Full‐length and truncated versions of rat TGN38/41 have been expressed in monkey (COS) and...

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Detalles Bibliográficos
Autores principales: Reaves, Barbara, Banting, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130381/
https://www.ncbi.nlm.nih.gov/pubmed/8082813
http://dx.doi.org/10.1016/0014-5793(94)00813-2
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author Reaves, Barbara
Banting, George
author_facet Reaves, Barbara
Banting, George
author_sort Reaves, Barbara
collection PubMed
description TGN38 and TGN41 are isoforms of a monotopic integral membrane protein which recycles between the trans Golgi network (TGN) and the cell surface, but which, at steady state, is predominantly located in the TGN. Full‐length and truncated versions of rat TGN38/41 have been expressed in monkey (COS) and human (Heb7a) cells under the control of the heavy metal inducible Metallothionein IIA promoter. This has allowed the regulated expression of TGN38/41 protein constructs to different levels in the transfected cells. These studies show that (i) controlled overexpression of TGN38/41 results in mislocalisation to parts of the endocytic pathway, (ii) a truncated version of TGN38/41, lacking the cytoplasmic domain, remains in the TGN, and (iii) there is a direct or indirect interaction between the cytoplasmic domain of TGN38/41 and γ‐adaptin.
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spelling pubmed-71303812020-04-08 Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin Reaves, Barbara Banting, George FEBS Lett Full‐length Articles TGN38 and TGN41 are isoforms of a monotopic integral membrane protein which recycles between the trans Golgi network (TGN) and the cell surface, but which, at steady state, is predominantly located in the TGN. Full‐length and truncated versions of rat TGN38/41 have been expressed in monkey (COS) and human (Heb7a) cells under the control of the heavy metal inducible Metallothionein IIA promoter. This has allowed the regulated expression of TGN38/41 protein constructs to different levels in the transfected cells. These studies show that (i) controlled overexpression of TGN38/41 results in mislocalisation to parts of the endocytic pathway, (ii) a truncated version of TGN38/41, lacking the cytoplasmic domain, remains in the TGN, and (iii) there is a direct or indirect interaction between the cytoplasmic domain of TGN38/41 and γ‐adaptin. John Wiley and Sons Inc. 1994-09-12 2001-10-18 /pmc/articles/PMC7130381/ /pubmed/8082813 http://dx.doi.org/10.1016/0014-5793(94)00813-2 Text en FEBS Letters 351 (1994) 1873-3468 © 2015 Federation of European Biochemical Societies This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Full‐length Articles
Reaves, Barbara
Banting, George
Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin
title Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin
title_full Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin
title_fullStr Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin
title_full_unstemmed Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin
title_short Overexpression of TGN38/41 leads to mislocalisation of γ‐adaptin
title_sort overexpression of tgn38/41 leads to mislocalisation of γ‐adaptin
topic Full‐length Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130381/
https://www.ncbi.nlm.nih.gov/pubmed/8082813
http://dx.doi.org/10.1016/0014-5793(94)00813-2
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