The Effect of Cap Structure and Poly(A) Positioning on mRNA Translation Efficiency

M Mizuki Tada (Department of Chemistry, Graduate School of Science, Research Center for Materials Science, and Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University, Nagoya, Aichi 464-8602, Japan) N Naoko Abe M Masahito Inagaki (Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan) Y Yuko Nakashima S Sana Ohashi (Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan) H Haruka Hiraoka (Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan) P Priyanka Uttamrao Deshmukh (Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan) N Naoyuki Yamane (Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan) N Noriaki Matsubara (Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan) Y Yasuaki Kimura F Fumitaka Hashiya H Hiroshi Abe

Abstract

Abstract We investigated the relationship between mRNA structure and translation activity using our recently developed chemical method to add a cap structure to an oligonucleotide and a technique for purifying capped mRNAs via reversed‐phase high‐performance liquid chromatography (HPLC) employing a photoreactive tag. Specifically, we designed and synthesized mRNA constructs in which the typical eukaryotic elements—the 5′ cap and the 3′ poly(A) tail—were interchanged in position. We examined how this inversion affected translation efficiency. The results revealed that this reversed configuration abolished the synergistic enhancement of translation typically observed with correctly positioned cap and poly(A) tail, resulting in a substantial decrease in activity compared to the native orientation. Interestingly, focusing solely on the cap structure, capping at the 3′ end—though less effective than at the 5′ end—still promoted a measurable increase in translation. Moreover, the poly(A) sequence placed at the 5′ end was found to suppress translation. We also prepared mRNAs containing a poly(A) tail with reversed 3′–5′ orientation and demonstrated that this inverted poly(A) could still enhance protein synthesis.

Article Details

Volume / Issue Vol. 64, Issue 50
Published December 08, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

M

Mizuki Tada

Department of Chemistry, Graduate School of Science, Research Center for Materials Science, and Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University, Nagoya, Aichi 464-8602, Japan

N

Naoko Abe

M

Masahito Inagaki

Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan

Y

Yuko Nakashima

S

Sana Ohashi

Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan

H

Haruka Hiraoka

Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan

P

Priyanka Uttamrao Deshmukh

Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan

N

Naoyuki Yamane

Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan

N

Noriaki Matsubara

Department of Chemistry Graduate School of Science Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8602 Japan

Y

Yasuaki Kimura

F

Fumitaka Hashiya

H

Hiroshi Abe