DNA methylation: a secondary event in globin gene switching?
Open Access
- 1 June 1988
- journal article
- research article
- Published by Cold Spring Harbor Laboratory in Genes & Development
- Vol. 2 (6) , 698-706
- https://doi.org/10.1101/gad.2.6.698
Abstract
Changes in gamma-globin gene methylation accompany the fetal to adult globin switch in man. Using somatic cell hybrids made by fusing mouse erythroleukemia and human fetal erythroid cells, we asked whether methylation is a cause or a consequence of gamma-gene inactivation during development. These hybrids initially express human gamma-globin but switch with time in culture to adult globin gene production. In hybrids before the switch, the gamma-genes are unmethylated. After completion of the switch, the hybrids contain methylated gamma-globin genes. However, during the time that the gamma----beta switch is occurring, hybrids are found that no longer express gamma-globin, yet still possess unmethylated gamma-globin genes. This suggests that methylation is not a primary event in gamma-gene inactivation during human development.Keywords
This publication has 31 references indexed in Scilit:
- Methylation of the Hprt gene on the inactive X occurs after chromosome inactivationCell, 1987
- Analysis of human hemoglobin switching in MEL × human fetal erythroid cell hybridsCell, 1986
- Methylation and the X chromosomeBioEssays, 1986
- DNA methylation and the regulation of globin gene expressionCell, 1983
- DNA Methylation and Gene FunctionScience, 1980
- Beta thalassemia: Mutations which affect processing of the β-globin mRNA precursorCell, 1980
- DNA methylation in the human γδβ-globin locus in erythroid and nonerythroid tissuesCell, 1980
- Specific DNA methylation sites in the vicinity of the chicken β-globin genesNature, 1979
- Occurrence of an intracellular inhibitor of ectosialyltransferase in lymphocytesFEBS Letters, 1977
- Changes in size and secondary structure of the ribosomal transcription unit during vertebrate evolutionJournal of Molecular Biology, 1975