Abstract
Acanthamoeba rRNA transcription involves the binding of a transcription initiation factor (TIF) to the core promoter of rDNA to form the preinitiation complex. This complex is formed in the absence of RNA polymerase I, and persists for multiple rounds of initiation. Polymerase I next binds to form the initiation complex. This binding is DNA sequence-independent, and is directed by protein-protein contacts with TIF. DNA melting occurs in a separate step. In contrast to most prokaryotic transcription, melting occurs only following nucleotide addition and β-γ hydrolysis of ATP is not required as for polymerase II. Growth-dependent regulation of rRNA transcription is accomplished by modification of RNA polymerase I. The inactive form of polymerase (PolE) is unable to bind to the promoter and has altered heat stability. PolE is still active in elongation; thus, the modification affects the polymerase site involved in TIF contact. Modification of a polymerases I and III common subunit has been detected leading to the suggestion that transcription of stable RNAs of the ribosome might be co-regulated by this mechanism.
Dedicated to the memory of Preecha Kownin
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Paule, M.R. et al. (1991). Initiation and regulation mechanisms of ribosomal RNA transcription in the eukaryote acanthamoeba castellanii. In: Morgan, H.E. (eds) Molecular Mechanisms of Cellular Growth. Developments in Molecular and Cellular Biochemistry, vol 7. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3886-8_15
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DOI: https://doi.org/10.1007/978-1-4615-3886-8_15
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