Skip to main navigation Skip to search Skip to main content

Impact of template backbone heterogeneity on RNA polymerase II transcription

  • Liang Xu
  • , Wei Wang
  • , Lu Zhang
  • , Jenny Chong
  • , Xuhui Huang
  • , Dong Wang*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Articlepeer-review

Abstract

Variations in the sugar component (ribose or deoxyribose) and the nature of the phosphodiester linkage (3'-5' or 2'-5' orientation) have been a challenge for genetic information transfer from the very beginning of evolution. RNA polymerase II (pol II) governs the transcription of DNA into precursor mRNA in all eukaryotic cells. How pol II recognizes DNA template backbone (phosphodiester linkage and sugar) and whether it tolerates the backbone heterogeneity remain elusive. Such knowledge is not only important for elucidating the chemical basis of transcriptional fidelity but also provides new insights into molecular evolution. In this study, we systematically and quantitatively investigated pol II transcriptional behaviors through different template backbone variants. We revealed that pol II can well tolerate and bypass sugar heterogeneity sites at the template but stalls at phosphodiester linkage heterogeneity sites. The distinct impacts of these two backbone components on pol II transcription reveal the molecular basis of template recognition during pol II transcription and provide the evolutionary insight from the RNA world to the contemporary 'imperfect' DNA world. In addition, our results also reveal the transcriptional consequences from ribose-containing genomic DNA.

Original languageEnglish
Pages (from-to)2232-2241
Number of pages10
JournalNucleic Acids Research
Volume43
Issue number4
DOIs
Publication statusPublished - 27 Feb 2015

Bibliographical note

Publisher Copyright:
© 2015 The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.

Fingerprint

Dive into the research topics of 'Impact of template backbone heterogeneity on RNA polymerase II transcription'. Together they form a unique fingerprint.

Cite this