Abstract
The kinetics of ribosomal RNA transcription and processing were assessed in chronic lymphocytic leukemia (CLL) lymphocytes during the initial phases of their delayed response to phytohemagglutinin. When compared to cultures of normal lymphocytes, CLL cultures developed normal augmentations in 45S rRNA precursor transcription and cleavage after a 1 hr incubation with PHA. However, failure to conserve 18S RNA subunits persisted in the CLL cultures. Subsequently the PHA-induced progressive rise in 45S RNA transcription became aborted and the over-all rate of RNA synthesis lagged far behind the levels attained by normal cultures incubated with PHA for 48 hr. CLL cultures responding to PHA in a delayed fashion exhibited efficient conservation of 18S RNA at 168 hr. In normal cultures, PHA-induced conservation of 18S RNA appeared to be independent of any effect on 45S ribosomal RNA precursor transcription. Therefore, the sluggish growth response of CLL lymphocytes was associated with a defect in one of the important mechanisms regulating assembly of new ribosomes.
MeSH Terms
Adult
Cells, Cultured
DNA/analysis
Genetic Code
Humans
In Vitro Techniques
Lectins/pharmacology
Leukemia, Lymphoid/blood
Lymphocyte Activation
Lymphocytes/metabolism
Methionine/metabolism
Methods
Methylation
Middle Aged
RNA, Ribosomal/analysis,metabolism
RNA, Transfer/analysis,metabolism
Ribosomes
Time Factors
Tritium
Ultracentrifugation
Uridine/metabolism
Chemicals
Lectins
RNA, Ribosomal
Tritium
DNA
RNA, Transfer
Methionine
Uridine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Rubin A D
References (12)
12 references, click to expand
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