Abstract
Cell-free extracts of lymphosarcoma P1798 cell culture lines support faithful initiation upon the cloned mouse DNA encoding rRNA (rDNA) promoter, whereas extracts from cells treated for 16 hr with 0.1 microM dexamethasone cannot. Extracts from both sources transcribe the cloned 5S RNA gene in vitro and mixing experiments further demonstrate that inhibition of transcription of rDNA in vitro is not due to nucleases or inhibitors of transcription present in extracts from glucocorticoid-treated cells. Incubation of extracts from control cells at 45 degrees C for 15 min inactivates RNA polymerase I and abolishes transcription. Activity can be restored by the addition of partially purified RNA polymerase I from control cells and hormone-treated cells. Moreover, extracts from hormone treated cells can be reconstituted by the addition of a partially purified, heat-stable transcription factor from control cells.
MeSH Terms
Animals
Cell Line
Cricetinae
DNA/genetics
DNA Restriction Enzymes
DNA, Ribosomal
Dexamethasone/pharmacology
Genes/drug effects
Lymphoma, Non-Hodgkin/metabolism
Mesocricetus
Mice
Mice, Inbred BALB C
Plasmids
RNA Polymerase I/antagonists & inhibitors
RNA, Ribosomal/genetics
Transcription, Genetic/drug effects
Chemicals
DNA, Ribosomal
RNA, Ribosomal
Dexamethasone
DNA
RNA Polymerase I
DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Cavanaugh A H
Gokal P K
Lawther R P
Thompson E A
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16 references, click to expand
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