Abstract
Two Drosophila tRNALys genes with identical coding sequences were shown to transcribe with very different efficiences in nuclear extracts from Xenopus oocytes. The use of recombinant plasmids in which the 5'-flanking sequences of these genes were either "switched" or replaced by defined pBR322 sequences revealed two control regions for tRNA gene transcription. An internal control region comprising the mature tRNA coding sequence (and possibly its 3'-flanking sequences) is sufficient for transcription initiation, and an external control region comprising the 5'-flanking sequences represses this transcription. All transcripts have short leader sequences. Altered precursor tRNAs transcribed from truncated tRNALys genes (missing a single base pair in the acceptor stem) are not processed well in vitro.
MeSH Terms
Animals
Base Sequence
Cloning, Molecular
DNA, Recombinant/metabolism
Drosophila melanogaster/genetics
Electrophoresis, Polyacrylamide Gel
Escherichia coli/genetics
Female
Gene Expression Regulation
Models, Genetic
Oocytes/metabolism
Plasmids
RNA, Transfer/genetics
Templates, Genetic
Transcription, Genetic
Xenopus/cytology
Chemicals
DNA, Recombinant
RNA, Transfer
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
DeFranco D
Schmidt O
Söll D
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24 references, click to expand
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