Affiliation:
1. State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, People's Republic of China
Abstract
ABSTRACT
Basal elements in archaeal promoters, except for putative initiator elements encompassing transcription start sites, are well characterized. Here, we employed the
Sulfolobus
araS
promoter as a model to study the function of the initiator element (Inr) in archaea. We have provided evidence for the presence of a third core promoter element, the
Sulfolobus
Inr, whose action depends on a TATA box and the TF
B
r
ecognition
e
lement (BRE). Substitution mutations in the
araS
Inr did not alter the location of the transcription start site. Using systematic mutagenesis, the most functional
araS
Inr was defined as +1 GAGAMK +6 (where M is A/C and K is G/T). Furthermore, WebLogo analysis of a subset of promoters with coding sequences for 5′ untranslated regions (UTRs) larger than 4 nucleotides (nt) in
Sulfolobus solfataricus
P2 identified an Inr consensus that exactly matches the functional
araS
Inr sequence. Moreover, mutagenesis of 3 randomly selected promoters confirmed the Inr sequences to be important for basal promoter strength in the subgroup. Importantly, the result of the
araS
Inr being added to the Inr-less promoters indicates that the
araS
Inr, the core promoter element, is able to enhance the strength of Inr-less promoters. We infer that transcription factor B (TFB) and subunits of RNA polymerase bind the Inr to enhance promoter strength. Taken together, our data suggest that the presence or absence of an Inr on basal promoters is important for global gene regulation in
Sulfolobus
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
18 articles.
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