Evidence map›Paper›PMID 41020503›Full record

ArticleNucleic acids research2025

Modified unlocked nucleic acid (MUNA) mitigates off-target effects of small interfering RNAs.

Shohei Mori, Dhrubajyoti Datta, Lydia Perkins, Michelle Jung, Lauren Blair Woods, Alex Eaton, June Qin, Tim Racie, MaryBeth Kim, Dale C Guenther and 6 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Shohei MoriAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.ORCID 0000-0001-8472-8055
Dhrubajyoti DattaAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Lydia PerkinsAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Michelle JungAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Lauren Blair WoodsAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Alex EatonAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
June QinAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Tim RacieAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
MaryBeth KimAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Dale C GuentherAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Adam CastorenoAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Mark K SchlegelAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.ORCID 0000-0002-0127-608X
Klaus CharisseAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Martin EgliDepartment of Biochemistry and Center for Structural Biology, Vanderbilt University, School of Medicine, Nashville, TN 37232-0146, United States.ORCID 0000-0003-4145-356X
Shigeo MatsudaAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.
Muthiah ManoharanAlnylam Pharmaceuticals, 675 West Kendall, Cambridge, MA 02142, United States.ORCID 0000-0002-7931-1172

Funding

Alnylam Pharmaceuticals
6 · The paper itself

Abstract

Unlocked nucleic acid (UNA) is a nucleic acid analog that has an acyclic ribose ring lacking the bond between C2' and C3' atoms. The base-pairing properties of UNA have been studied, and it has been used as a scaffold for conjugation, but the chemical space around UNA and its potential applications in the context of short interfering RNAs (siRNAs), which mediate RNA interference, have not been thoroughly explored. In this study, we report syntheses of methylated and methoxylated UNAs and their incorporation into siRNAs. siRNAs with 5'-(R)-methyl-UNA and with 5'-(S)-methyl-UNA in the seed region had comparable potencies but reduced off-target effects compared to siRNA modified with UNA. In mice, siRNAs with modified UNAs were of comparable potency to an siRNA of the same sequence and chemistry lacking UNA. Modeling studies indicated that the flexibilities of UNA and the modified UNAs facilitate kinking of the antisense strand when incorporated at position 7. These findings highlight the potential of modified UNA for advancing therapeutics that act through the RNA interference pathway.

Indexed as

Nucleic AcidsRNA InterferenceRNA, Small InterferingAnimalsBase PairingHumansMiceNucleic Acid ConformationNucleic AcidsRNA, Small Interfering

Identifiers

PMID41020503
PMCPMC12477598

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.