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DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues
CpG-island margins and non-island-CpG sites round the transcription start sites of CpG-island-positive and -negative genes are methylated to various degrees in a tissue-specific manner. These methylation-variable CpG sites were analyzed to delineate a relationship between the methylation and transcr...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752778/ https://www.ncbi.nlm.nih.gov/pubmed/19794993 http://dx.doi.org/10.3346/jkms.2009.24.5.918 |
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author | Hong, Seung-Jin Kang, Moo-Il Oh, Jung-Hwan Jung, Yu-Chae Kim, Young-Ho Kim, Sung-Ja Choi, Seung-Hye Seo, Eun-Joo Choi, Sang-Wook Rhyu, Mun-Gan |
author_facet | Hong, Seung-Jin Kang, Moo-Il Oh, Jung-Hwan Jung, Yu-Chae Kim, Young-Ho Kim, Sung-Ja Choi, Seung-Hye Seo, Eun-Joo Choi, Sang-Wook Rhyu, Mun-Gan |
author_sort | Hong, Seung-Jin |
collection | PubMed |
description | CpG-island margins and non-island-CpG sites round the transcription start sites of CpG-island-positive and -negative genes are methylated to various degrees in a tissue-specific manner. These methylation-variable CpG sites were analyzed to delineate a relationship between the methylation and transcription of the tissue-specific genes. The level of tissue-specific transcription was estimated by counting the number of the total transcripts in the SAGE (serial analysis of gene expression) database. The methylation status of 12 CpG-island margins and 21 non-island CpG sites near the key tissue-specific genes was examined in pluripotent stromal cells obtained from fat and bone marrow samples as well as in lineage-committed cells from marrow bulk, stomach, colon, breast, and thyroid samples. Of the 33 CpG sites examined, 10 non-island-CpG sites, but none of the CpG-island margins were undermethylated concurrent with tissue-specific expression of their nearby genes. The net methylation of the 33 CpG sites and the net amount of non-island-CpG gene transcripts were high in stomach tissues and low in stromal cells. The present findings suggest that the methylation of the non-island-CpG sites is inversely associated with the expression of the nearby genes, and the concert effect of transitional-CpG methylation is linearly associated with the stomach-specific genes lacking CpG-islands. |
format | Text |
id | pubmed-2752778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-27527782009-10-01 DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues Hong, Seung-Jin Kang, Moo-Il Oh, Jung-Hwan Jung, Yu-Chae Kim, Young-Ho Kim, Sung-Ja Choi, Seung-Hye Seo, Eun-Joo Choi, Sang-Wook Rhyu, Mun-Gan J Korean Med Sci Original Article CpG-island margins and non-island-CpG sites round the transcription start sites of CpG-island-positive and -negative genes are methylated to various degrees in a tissue-specific manner. These methylation-variable CpG sites were analyzed to delineate a relationship between the methylation and transcription of the tissue-specific genes. The level of tissue-specific transcription was estimated by counting the number of the total transcripts in the SAGE (serial analysis of gene expression) database. The methylation status of 12 CpG-island margins and 21 non-island CpG sites near the key tissue-specific genes was examined in pluripotent stromal cells obtained from fat and bone marrow samples as well as in lineage-committed cells from marrow bulk, stomach, colon, breast, and thyroid samples. Of the 33 CpG sites examined, 10 non-island-CpG sites, but none of the CpG-island margins were undermethylated concurrent with tissue-specific expression of their nearby genes. The net methylation of the 33 CpG sites and the net amount of non-island-CpG gene transcripts were high in stomach tissues and low in stromal cells. The present findings suggest that the methylation of the non-island-CpG sites is inversely associated with the expression of the nearby genes, and the concert effect of transitional-CpG methylation is linearly associated with the stomach-specific genes lacking CpG-islands. The Korean Academy of Medical Sciences 2009-10 2009-09-23 /pmc/articles/PMC2752778/ /pubmed/19794993 http://dx.doi.org/10.3346/jkms.2009.24.5.918 Text en Copyright © 2009 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hong, Seung-Jin Kang, Moo-Il Oh, Jung-Hwan Jung, Yu-Chae Kim, Young-Ho Kim, Sung-Ja Choi, Seung-Hye Seo, Eun-Joo Choi, Sang-Wook Rhyu, Mun-Gan DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues |
title | DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues |
title_full | DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues |
title_fullStr | DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues |
title_full_unstemmed | DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues |
title_short | DNA Methylation and Expression Patterns of Key Tissue-specific Genes in Adult Stem Cells and Stomach Tissues |
title_sort | dna methylation and expression patterns of key tissue-specific genes in adult stem cells and stomach tissues |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752778/ https://www.ncbi.nlm.nih.gov/pubmed/19794993 http://dx.doi.org/10.3346/jkms.2009.24.5.918 |
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