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hTR repressor-related gene on human chromosome 10p15.1
Somatic cells express genes that suppress telomerase activity and these genes may be inactivated in tumour cells. We postulated that cancer cells acquire immortality by activation of telomerase by the loss of such a gene. We have reported recently that a telomerase repressor gene may be located on 1...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363951/ https://www.ncbi.nlm.nih.gov/pubmed/11720437 http://dx.doi.org/10.1054/bjoc.2001.2121 |
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author | Miura, N Onuki, N Rathi, A Virmani, A Nakamoto, S Kishimoto, Y Murawaki, Y Kawasaki, H Hasegawa, J Oshimura, M Travis, W D Gazdar, A F |
author_facet | Miura, N Onuki, N Rathi, A Virmani, A Nakamoto, S Kishimoto, Y Murawaki, Y Kawasaki, H Hasegawa, J Oshimura, M Travis, W D Gazdar, A F |
author_sort | Miura, N |
collection | PubMed |
description | Somatic cells express genes that suppress telomerase activity and these genes may be inactivated in tumour cells. We postulated that cancer cells acquire immortality by activation of telomerase by the loss of such a gene. We have reported recently that a telomerase repressor gene may be located on 10p15.1 by deletion mapping using microcell-mediated chromosome transfer (MMCT), radiated microcell fusion (RMF), fluorescent in situ hybridization (FISH) and STS analysis. To independently confirm this result, we correlated expression of RNA component of telomerase (hTR) as a marker of telomerase expression by in situ hybridization with allelic loss in pulmonary carcinoid tumours. Unlike most malignant tumours, pulmonary carcinoids (which are low-grade malignant tumours) are heterogeneous for telomerase expression. Loss of 5 closely spaced polymorphic markers on 10p15.1, especially D10S1728, were highly correlated with hTR expression. In an additional experiment, 10p15.1 showed higher and more significant correlation than any region of 3p where it has been predicted as another chromosomal location of telomerase repressor with allelic loss of the region. Our findings strongly suggest that 10p15.1 harbours a gene involved in repression of telomerase RNA component in human somatic cells and each putative repressor (on 3p and 10p) may act independently. © 2001 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2363951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23639512009-09-10 hTR repressor-related gene on human chromosome 10p15.1 Miura, N Onuki, N Rathi, A Virmani, A Nakamoto, S Kishimoto, Y Murawaki, Y Kawasaki, H Hasegawa, J Oshimura, M Travis, W D Gazdar, A F Br J Cancer Regular Article Somatic cells express genes that suppress telomerase activity and these genes may be inactivated in tumour cells. We postulated that cancer cells acquire immortality by activation of telomerase by the loss of such a gene. We have reported recently that a telomerase repressor gene may be located on 10p15.1 by deletion mapping using microcell-mediated chromosome transfer (MMCT), radiated microcell fusion (RMF), fluorescent in situ hybridization (FISH) and STS analysis. To independently confirm this result, we correlated expression of RNA component of telomerase (hTR) as a marker of telomerase expression by in situ hybridization with allelic loss in pulmonary carcinoid tumours. Unlike most malignant tumours, pulmonary carcinoids (which are low-grade malignant tumours) are heterogeneous for telomerase expression. Loss of 5 closely spaced polymorphic markers on 10p15.1, especially D10S1728, were highly correlated with hTR expression. In an additional experiment, 10p15.1 showed higher and more significant correlation than any region of 3p where it has been predicted as another chromosomal location of telomerase repressor with allelic loss of the region. Our findings strongly suggest that 10p15.1 harbours a gene involved in repression of telomerase RNA component in human somatic cells and each putative repressor (on 3p and 10p) may act independently. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-11 /pmc/articles/PMC2363951/ /pubmed/11720437 http://dx.doi.org/10.1054/bjoc.2001.2121 Text en Copyright © 2001 Cancer Research Campaign 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 | Regular Article Miura, N Onuki, N Rathi, A Virmani, A Nakamoto, S Kishimoto, Y Murawaki, Y Kawasaki, H Hasegawa, J Oshimura, M Travis, W D Gazdar, A F hTR repressor-related gene on human chromosome 10p15.1 |
title | hTR repressor-related gene on human chromosome 10p15.1 |
title_full | hTR repressor-related gene on human chromosome 10p15.1 |
title_fullStr | hTR repressor-related gene on human chromosome 10p15.1 |
title_full_unstemmed | hTR repressor-related gene on human chromosome 10p15.1 |
title_short | hTR repressor-related gene on human chromosome 10p15.1 |
title_sort | htr repressor-related gene on human chromosome 10p15.1 |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363951/ https://www.ncbi.nlm.nih.gov/pubmed/11720437 http://dx.doi.org/10.1054/bjoc.2001.2121 |
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