Abstract
Hybrids formed by fusing mouse erythroleukemia (MEL) cells with human fetal erythroid cells produce human fetal globin, but they switch to adult globin production as culture time advances. To obtain information on the chromosomal assignment of the elements that control γ-to-β switching, we analyzed the chromosomal composition of hybrids producing exclusively or predominantly human fetal globin and hybrids producing only adult human globin. No human chromosome was consistently absent in hybrids expressing fetal globin and consistently absent in hybrids expressing adult globin. Subcloning experiments demonstrated identical chromosomal compositions in subclones displaying the fetal globin program and those that had switched to expression of the adult globin program. These data indicate that retention of only one human chromosome - i.e., chromosome 11 - is sufficient for expression of human fetal globin and the subsequent γ-to-β switch. The results suggest that the γ-β switch is controlled either cis to the β-globin locus or by a trans-acting mechanism, the genes of which reside on human chromosome 11.
| Original language | English |
|---|---|
| Pages (from-to) | 8105-8109 |
| Number of pages | 5 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 84 |
| Issue number | 22 |
| DOIs | |
| State | Published - 1987 |
| Externally published | Yes |
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