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Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma.
In this study, reverse transcriptase polymerase chain reaction was used to amplify human endothelin receptor A (ETA) and ETB receptor mRNA. A truncated ETA receptor transcript with exons 3 and 4 skipped was found. The skipping of these two exons results in 109 amino acids being deleted from the rece...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group|1
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2062989/ https://www.ncbi.nlm.nih.gov/pubmed/9820169 |
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author | Zhang, Y. F. Jeffery, S. Burchill, S. A. Berry, P. A. Kaski, J. C. Carter, N. D. |
author_facet | Zhang, Y. F. Jeffery, S. Burchill, S. A. Berry, P. A. Kaski, J. C. Carter, N. D. |
author_sort | Zhang, Y. F. |
collection | PubMed |
description | In this study, reverse transcriptase polymerase chain reaction was used to amplify human endothelin receptor A (ETA) and ETB receptor mRNA. A truncated ETA receptor transcript with exons 3 and 4 skipped was found. The skipping of these two exons results in 109 amino acids being deleted from the receptor. The truncated receptor was expressed in all tissues and cells examined, but the level of expression varied. In melanoma cell lines and melanoma tissues, the truncated receptor gene was the major species, whereas the wild-type ETA was predominant in other tissues. A 1.9-kb ETA transcript was identified in melanoma cell lines by Northern blot, which was much smaller than the transcript in heart and in other tissues reported previously (4.3 kb). The cDNA coding regions of the truncated and wild-type ETA receptors were stably transfected into Chinese hamster ovary (CHO) cells. The truncated ETA receptor-transfected CHO cells did not show binding affinity to endothelin 1 (ET-1) or endothelin 3 (ET-3). The function and biological significance of this truncated ETA receptor is not clear, but it may have regulatory roles for cell responses to ETs. IMAGES: |
format | Text |
id | pubmed-2062989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Nature Publishing Group|1 |
record_format | MEDLINE/PubMed |
spelling | pubmed-20629892009-09-10 Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. Zhang, Y. F. Jeffery, S. Burchill, S. A. Berry, P. A. Kaski, J. C. Carter, N. D. Br J Cancer Research Article In this study, reverse transcriptase polymerase chain reaction was used to amplify human endothelin receptor A (ETA) and ETB receptor mRNA. A truncated ETA receptor transcript with exons 3 and 4 skipped was found. The skipping of these two exons results in 109 amino acids being deleted from the receptor. The truncated receptor was expressed in all tissues and cells examined, but the level of expression varied. In melanoma cell lines and melanoma tissues, the truncated receptor gene was the major species, whereas the wild-type ETA was predominant in other tissues. A 1.9-kb ETA transcript was identified in melanoma cell lines by Northern blot, which was much smaller than the transcript in heart and in other tissues reported previously (4.3 kb). The cDNA coding regions of the truncated and wild-type ETA receptors were stably transfected into Chinese hamster ovary (CHO) cells. The truncated ETA receptor-transfected CHO cells did not show binding affinity to endothelin 1 (ET-1) or endothelin 3 (ET-3). The function and biological significance of this truncated ETA receptor is not clear, but it may have regulatory roles for cell responses to ETs. IMAGES: Nature Publishing Group|1 1998-11 /pmc/articles/PMC2062989/ /pubmed/9820169 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Zhang, Y. F. Jeffery, S. Burchill, S. A. Berry, P. A. Kaski, J. C. Carter, N. D. Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. |
title | Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. |
title_full | Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. |
title_fullStr | Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. |
title_full_unstemmed | Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. |
title_short | Truncated human endothelin receptor A produced by alternative splicing and its expression in melanoma. |
title_sort | truncated human endothelin receptor a produced by alternative splicing and its expression in melanoma. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2062989/ https://www.ncbi.nlm.nih.gov/pubmed/9820169 |
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