Abstract

Although RNA modifications were discovered decades ago, the identification of enzymes that write, read, and erase RNA modifications enabled their functional study and spawned the field of epitranscriptomics. Coupling that knowledge to new methods has enabled the precise pinpointing of epitranscriptomic modifications across the transcriptome and the elucidation of their functional consequences. PCIF1 (Phosphorylated CTD-Interacting Factor 1) was shown to add N6, 2′-O-dimethyladenosine (m6Am) marks at the first nucleotide after the 5′ N7-methylguanosine (m7G) cap. In this chapter, we discuss the epitranscriptomic regulation of mRNA in general and focus on m7G cap-adjacent m6Am in particular. m6Am positions can now be distinguished from N6-methyladenosine (m6A) using new techniques leveraging PCIF1-knockout cells. Although m6Am modification sites can be detected precisely, conflicting data have been published regarding how cap-adjacent m6Am marks affect their host mRNA. Discrepancies in the data mean that the effects of cap-adjacent m6Am on mRNA stability, decapping, and translation continue to be debated. Finally, while PCIF1 is predominantly nuclear, a subset of results suggests a possible cytoplasmic role as well. Taken together, these contradictory results which employed different methodologies and cell lines mean that further experiments are required to determine the ultimate biological function(s) of m7G cap-adjacent m6Am.

Original languageEnglish (US)
Title of host publicationRNA Technologies
PublisherSpringer Science and Business Media Deutschland GmbH
Pages325-351
Number of pages27
DOIs
StatePublished - 2021

Publication series

NameRNA Technologies
Volume12
ISSN (Print)2197-9731
ISSN (Electronic)2197-9758

Keywords

  • Cap-adjacent mAm
  • Cytoplasmic capping
  • Epitranscriptome
  • N6 2′-O-dimethyladenosine
  • PCIF1

ASJC Scopus subject areas

  • Cancer Research
  • Biochemistry
  • Genetics
  • Molecular Biology
  • Biochemistry, medical

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