Abstract
Two recombinant plasmids, M4 and KH10, carrying Dictyostelium DNA inserted into the Eco RI restriction endonuclease site of pMB9 by poly(dA)-poly(dT) tailing, were selected for study because they are complementary to abundant mRNA populations from Dictyostelium. Both plasmids have been shown to hybridize a heterogeneous size class of mRNAs which, in the case of KH10, comprise 5-10% of the pulse-labeled poly(A)+ RNA from vegetative cells. Analysis of the sequence organization of the two pieces of Dictyostelium DNA shows that they consist mostly of single-copy sequences with a short DNA sequence which is repeated in the genome and interspersed with single-copy DNA. These and other results suggest that the majority of the hybridization of pulse-labeled mRNA to M4 and KH10 is to the short "repeated" DNA sequences. In the genome, members of these repeat families appear to be transcribed onto a population of different single-copy mRNAs. Additional results show that M4 DNA contains a sequence which is entirely complementary to a discrete mRNA.
MeSH Terms
Base Sequence
DNA Restriction Enzymes
DNA, Recombinant/metabolism
Dictyostelium/metabolism
Kinetics
Nucleic Acid Denaturation
Nucleic Acid Hybridization
Plasmids
Poly A/metabolism
Poly dA-dT
RNA, Messenger/biosynthesis
Transcription, Genetic
Chemicals
DNA, Recombinant
RNA, Messenger
Poly A
Poly dA-dT
DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kindle K L
Firtel R A
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