Transcription elongation factor SII

• Authors: Megan Wind, Emory University; Daniel Reines, Emory University
• Journal Title: BioEssays
• Volume: Volume 22, Number 4
• Publisher: Wiley: 12 months | 2000-04, Pages 327-336
• Type of Work: Article | Post-print: After Peer Review
• Publisher DOI: http://doi.org/10.1002/(SICI)1521-1878(200004)22:4<327::AID-BIES3>3.0.CO;2-4
• Subjects: Chemistry, Biochemistry

Abstract

RNA chain elongation by RNA polymerase II (pol II) is a complex and regulated process which is coordinated with capping, splicing, and polyadenylation of the primary transcript. Numerous elongation factors that enable pol II to transcribe faster and/or more efficiently have been purified. SII is one such factor. It helps pol II bypass specific blocks to elongation that are encountered during transcript elongation. SII was first identified biochemically on the basis of its ability to enable pol II to synthesize long transcripts.(1) Both the high resolution structure of SII and the details of its novel mechanism of action have been refined through mutagenesis and sophisticated in vitro assays. SII engages transcribing pol II and assists it in bypassing blocks to elongation by stimulating a cryptic, nascent RNA cleavage activity intrinsic to RNA polymerase. The nuclease activity can also result in removal of misincorporated bases from RNA. Molecular genetic experiments in yeast suggest that SII is generally involved in mRNA synthesis in vivo and that it is one type of a growing collection of elongation factors that regulate pol II. In vertebrates, a family of related SII genes has been identified; some of its members are expressed in a tissue-specific manner. The principal challenge now is to understand the isoform-specific functional differences and the biology of regulation exerted by the SII family of proteins on target genes, particularly in multicellular organisms.