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Active expression of G gamma globin gene on chromosome 11 with Yunnanese A gamma delta beta)0-thalassemia deletion in MEL cells.

Abstract
A permanent lymphocyte cell line of a heterozygote with Yunnanese (A gamma delta beta)0-thalassemia deletion, associated with an increased production of G gamma globin in adult, was founded using Epstein-Barr virus transformation. The hybrids of the lymphocyte cell and mouse erythroleukemia cell (MEL) were achieved and the hybrids containing human chromosome 11 were selected with the monoclonal antibody 53/6. The subclones containing only either the normal or the abnormal human chromosome 11 were separated and the expression of the human globin genes was studied. Expression of the beta-globin gene, but not the G gamma and A gamma, was observed in the hybrids containing only the normal human chromosome 11, while active expression of the G gamma globin gene was observed in the hybrids containing only the abnormal human chromosome 11. These results have confirmed that the DNA deletion in the beta-globin gene cluster is the cause of persistent active expression of the G gamma globin gene in the Yunnanese mutant.
AuthorsJ Zhang, J Qiao, W Song, Z Qiu
JournalScience in China. Series C, Life sciences (Sci China C Life Sci) Vol. 39 Issue 3 Pg. 329-36 (Jun 1996) ISSN: 1006-9305 [Print] China
PMID8760459 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Globins
Topics
  • Adult
  • Animals
  • Cell Fusion
  • Cell Line
  • Chromosomes, Human, Pair 11
  • Gene Deletion
  • Gene Expression
  • Globins (genetics)
  • Humans
  • Leukemia, Experimental (pathology)
  • Male
  • Mice
  • Thalassemia (genetics, pathology)
  • Tumor Cells, Cultured

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