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.
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Authors | J Zhang, J Qiao, W Song, Z Qiu |
Journal | Science 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 |
PMID | 8760459
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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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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