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Non-coding transcripts far upstream of the epsilon-globin gene are distinctly expressed in human primary tissues and erythroleukemia cell lines.

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.
AuthorsPing Xiang, Xiangdong Fang, Wenxuan Yin, Grainne Barkess, Qiliang Li
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 344 Issue 2 Pg. 623-30 (Jun 02 2006) ISSN: 0006-291X [Print] United States
PMID16620781 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Transcription Factors
  • Globins
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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