Regulation of Ribosomal RNA Production by RNA Polymerase I: Does Elongation Come First?
Author(s) -
Benjamin Albert,
Jorge Pérez-Fernández,
Isabelle LégerSilvestre,
Olivier Gadal
Publication year - 2012
Publication title -
genetics research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.351
H-Index - 9
eISSN - 2090-3154
pISSN - 2090-3162
DOI - 10.1155/2012/276948
Subject(s) - rna polymerase i , ribosomal rna , rna polymerase ii , rna , biology , chromatin , 5.8s ribosomal rna , elongation factor , microbiology and biotechnology , polymerase , transcription (linguistics) , rna polymerase , gene , genetics , ribosome , gene expression , promoter , linguistics , philosophy
Ribosomal RNA (rRNA) production represents the most active transcription in the cell. Synthesis of the large rRNA precursors (35–47S) can be achieved by up to 150 RNA polymerase I (Pol I) enzymes simultaneously transcribing each rRNA gene. In this paper, we present recent advances made in understanding the regulatory mechanisms that control elongation. Built-in Pol I elongation factors, such as Rpa34/Rpa49 in budding yeast and PAF53/CAST in humans, are instrumental to the extremely high rate of rRNA production per gene. rRNA elongation mechanisms are intrinsically linked to chromatin structure and to the higher-order organization of the rRNA genes (rDNA). Factors such as Hmo1 in yeast and UBF1 in humans are key players in rDNA chromatin structure in vivo . Finally, elongation factors known to regulate messengers RNA production by RNA polymerase II are also involved in rRNA production and work cooperatively with Rpa49 in vivo .
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