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Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering
Telomerase is a ribonucleoprotein enzyme that synthesizes telomeric DNA. The reactivation of telomerase activity by aberrant upregulation/expression of its catalytic subunit hTERT is a major pathway in human tumorigenesis. However, regulatory mechanisms that control hTERT expression are largely unkn...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907559/ https://www.ncbi.nlm.nih.gov/pubmed/20678252 http://dx.doi.org/10.1186/2041-9414-1-6 |
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author | Abe, Satoshi Tanaka, Hiromi Notsu, Tomomi Horike, Shin-ichi Fujisaki, Chikako Qi, Dong-Lai Ohhira, Takahito Gilley, David Oshimura, Mitsuo Kugoh, Hiroyuki |
author_facet | Abe, Satoshi Tanaka, Hiromi Notsu, Tomomi Horike, Shin-ichi Fujisaki, Chikako Qi, Dong-Lai Ohhira, Takahito Gilley, David Oshimura, Mitsuo Kugoh, Hiroyuki |
author_sort | Abe, Satoshi |
collection | PubMed |
description | Telomerase is a ribonucleoprotein enzyme that synthesizes telomeric DNA. The reactivation of telomerase activity by aberrant upregulation/expression of its catalytic subunit hTERT is a major pathway in human tumorigenesis. However, regulatory mechanisms that control hTERT expression are largely unknown. Previously, we and others have demonstrated that the introduction of human chromosome 3, via microcell-mediated chromosome transfer (MMCT), repressed transcription of the hTERT gene. These results suggested that human chromosome 3 contains a regulatory factor(s) involved in the repression of hTERT. To further localize this putative hTERT repressor(s), we have developed a unique experimental approach by introducing various truncated chromosome 3 regions produced by a novel chromosomal engineering technology into the renal cell carcinoma cell line (RCC23 cells). These cells autonomously express ectopic hTERT (exohTERT) promoted by a retroviral LTR promoter in order to permit cellular division after repression of endogenous hTERT. We found a telomerase repressor region located within a 7-Mb interval on chromosome 3p21.3. These results provide important information regarding hTERT regulation and a unique method to identify hTERT repressor elements. |
format | Text |
id | pubmed-2907559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29075592010-07-29 Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering Abe, Satoshi Tanaka, Hiromi Notsu, Tomomi Horike, Shin-ichi Fujisaki, Chikako Qi, Dong-Lai Ohhira, Takahito Gilley, David Oshimura, Mitsuo Kugoh, Hiroyuki Genome Integr Research Telomerase is a ribonucleoprotein enzyme that synthesizes telomeric DNA. The reactivation of telomerase activity by aberrant upregulation/expression of its catalytic subunit hTERT is a major pathway in human tumorigenesis. However, regulatory mechanisms that control hTERT expression are largely unknown. Previously, we and others have demonstrated that the introduction of human chromosome 3, via microcell-mediated chromosome transfer (MMCT), repressed transcription of the hTERT gene. These results suggested that human chromosome 3 contains a regulatory factor(s) involved in the repression of hTERT. To further localize this putative hTERT repressor(s), we have developed a unique experimental approach by introducing various truncated chromosome 3 regions produced by a novel chromosomal engineering technology into the renal cell carcinoma cell line (RCC23 cells). These cells autonomously express ectopic hTERT (exohTERT) promoted by a retroviral LTR promoter in order to permit cellular division after repression of endogenous hTERT. We found a telomerase repressor region located within a 7-Mb interval on chromosome 3p21.3. These results provide important information regarding hTERT regulation and a unique method to identify hTERT repressor elements. BioMed Central 2010-05-26 /pmc/articles/PMC2907559/ /pubmed/20678252 http://dx.doi.org/10.1186/2041-9414-1-6 Text en Copyright ©2010 Abe et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Abe, Satoshi Tanaka, Hiromi Notsu, Tomomi Horike, Shin-ichi Fujisaki, Chikako Qi, Dong-Lai Ohhira, Takahito Gilley, David Oshimura, Mitsuo Kugoh, Hiroyuki Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering |
title | Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering |
title_full | Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering |
title_fullStr | Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering |
title_full_unstemmed | Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering |
title_short | Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering |
title_sort | localization of an htert repressor region on human chromosome 3p21.3 using chromosome engineering |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907559/ https://www.ncbi.nlm.nih.gov/pubmed/20678252 http://dx.doi.org/10.1186/2041-9414-1-6 |
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