Abstract
Mutagenized DNA templates and HeLa whole cell extracts were used to study the effects of promoter-specific base changes on in vitro transcription. DNA templates where the initiating adenine (+1) was changed to thymidine (AT+1) in the adenovirus 2 major late transcription unit were transcribed with 50% efficiency of the unaltered template. We have described a mutant at the TATA box, where the A at position -28 was changed to a C (AC-28). Transcription efficiency was reduced to less than 20% of control in the AC-28 mutant (Concino et al., 1983, J. Biol. Chem. 258: 8493-8496). Primer extension analysis revealed increased 5' end heterogeneity for in vitro transcripts derived from AC-28 and AT+1 DNA templates. Specific transcription was completely abolished from AT+1 DNA templates when a second change was introduced within the TATA sequence, creating a double mutant (AC-28 . AT+1). Neither the AC-28 nor the AT+1 change alone had such an effect, suggesting a coordinated interaction in transcription initiation involving both the TATA box and the initiation site.
MeSH Terms
Adenoviruses, Human/genetics
Chromosome Mapping
Gene Expression Regulation
HeLa Cells
Promoter Regions, Genetic
RNA Polymerase II/genetics
RNA, Messenger/genetics
Transcription, Genetic
Chemicals
RNA, Messenger
RNA Polymerase II
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Concino M F
Lee R F
Merryweather J P
Weinmann R
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