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A model based on DNA methylation is proposed to explain the initiation and maintenance of mammalian X inactivation and certain aspects of other permanent events in eukaryotic cell differentiation. A key feature of the model is the proposal of sequence-specific DNA methylases that methylate unmethylated sites with great difficulty but easily methylate half-methylated sites. Although such enzymes have not yet been detected in eukaryotes, they are known in bacteria. An argument is presented, based on recent data on DNA-binding proteins, that DNA methylation should affect the binding of regulatory proteins. In support of the model, short reviews are included covering both mammalian X inactivation and bacterial restriction and modification enzymes.
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Arthur D. Riggs (Wed,) studied this question.
synapsesocial.com/papers/69daa83f00ab073a27838c02 — DOI: https://doi.org/10.1159/000130315
Arthur D. Riggs
City Of Hope National Medical Center
Cytogenetic and Genome Research
City Of Hope National Medical Center
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