Site-specific RNA modification via initiation of in vitro transcription reactions with m6A and isomorphic emissive adenosine analogs

Author:

Cong Deyuan1,Steinbuch Kfir B.1ORCID,Koyama Ryosuke1,Lam Tyler V.1,Lam Jamie Y.1,Tor Yitzhak1ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093-0358, USA

Abstract

Transcription reactions with excess adenosine surrogates leads to 5′-end modified transcripts, which can be ligated to diverse RNAs. By modifying a key position in a MazF RNA substrate, insight into the folding and recognition features is gained.

Funder

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

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