Abstract |
Non-coding exons of epsilon-globin mRNA originating within the 236 kb upstream region of the epsilon-globin gene were identified in human primary tissues and K562 cells. One predominant type of upstream epsilon mRNA, which originated in the -76 kb region 5' to the epsilon gene, was present in human primary tissues, whereas 11 other isoforms were identified in K562 cells. Fragment from the -76 kb region possessed promoter activity and a prominent DNase I hypersensitive site was formed in the region approximately 2 kb 5' to the -76 kb promoter in human fetal liver, but not in K562 cells. The promoter activity in the -236 kb region resided in a retrotransposon in K562 cells. A DNase I hypersensitive site was formed at the -236 kb promoter in K562 cells, but not in human fetal liver. We discussed these results in the context of intergenic transcription and chromatin opening in the beta-globin gene cluster.
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Authors | Ping Xiang, Xiangdong Fang, Wenxuan Yin, Grainne Barkess, Qiliang Li |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 344
Issue 2
Pg. 623-30
(Jun 02 2006)
ISSN: 0006-291X [Print] United States |
PMID | 16620781
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Transcription Factors
- Globins
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Topics |
- Cell Line, Tumor
- Gene Expression Regulation
- Globins
(genetics, metabolism)
- Humans
- Leukemia, Erythroblastic, Acute
(genetics, metabolism)
- Open Reading Frames
(genetics)
- Organ Specificity
- Tissue Distribution
- Transcription Factors
(genetics, metabolism)
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