Abstract
Histone mRNA from S. cerevisiae has been identified and partially purified. The RNA is quantitatively retained on oligo (dT) cellulose or poly(U) sepharose as assayed by in vitro translation or hybridization of radiolabelled cloned yeast histone sequences to RNA immobilized on DBM paper. Retention of yeast histone mRNA on either of these chromatographic systems is most likely the result of polyadenylation since, when primed with oligo (dT), the RNA is an extremely good template for reverse transcriptase, as determined by hybrid arrest translation or by hybridization to D. melanogaster histone DNA sequences.
MeSH Terms
Base Sequence
Chromatography, Affinity
Cloning, Molecular
Histones/genetics
Nucleic Acid Hybridization
Poly A/genetics
Protein Biosynthesis
RNA, Messenger/genetics,isolation & purification
Saccharomyces cerevisiae/genetics
Chemicals
Histones
RNA, Messenger
Poly A
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fahrner K
Yarger J
Hereford L
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