Abstract
The mechanisms that modulate c-myb mRNA levels in mouse erythroleukemia cells induced toward erythroid differentiation were compared with those that act on c-myc. Both genes exhibited regulation at the levels of premature transcription arrest and RNA turnover. However, these common processes allowed temporally distinct control of gene expression.
MeSH Terms
Animals
DNA Restriction Enzymes
Dimethyl Sulfoxide/pharmacology
Gene Expression Regulation/drug effects
Kinetics
Leukemia, Erythroblastic, Acute/genetics
Leukemia, Experimental/genetics
Mice
Nucleic Acid Hybridization
Proto-Oncogenes/drug effects
RNA, Messenger/drug effects,genetics
Transcription, Genetic/drug effects
Chemicals
RNA, Messenger
DNA Restriction Enzymes
Dimethyl Sulfoxide
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Watson R J
Imperial Cancer Research Fund Laboratories, St. Bartholomew's Hospital, Bartholomew Close, London, United Kingdom.
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