Effect of 2′-5′/3′-5′ phosphodiester linkage heterogeneity on RNA interference

Author:

Habibian Maryam1,Harikrishna S2,Fakhoury Johans1,Barton Maria3,Ageely Eman A4,Cencic Regina5,Fakih Hassan H1,Katolik Adam1,Takahashi Mayumi6,Rossi John6,Pelletier Jerry5ORCID,Gagnon Keith T34,Pradeepkumar P I2,Damha Masad J1ORCID

Affiliation:

1. Department of Chemistry, McGill University, 801 Sherbrooke St. West, Montreal, QC H3A 0B8, Canada

2. Department of Chemistry, Indian Institute of Technology Bombay, Mumbai 400076, India

3. Department of Biochemistry and Molecular Biology, Southern Illinois University School of Medicine, Carbondale, IL, USA

4. Department of Chemistry and Biochemistry, Southern Illinois University, Carbondale, IL, USA

5. Department of Biochemistry and Goodman Cancer Center, McGill University, Montreal, QC H3G 1Y6, Canada

6. Department of Molecular and Cellular Biology, Beckman Research Institute of City of Hope, Duarte, CA, USA

Abstract

Abstract We report on the synthesis of siRNAs containing both 2′-5′- and 3′-5′-internucleotide linkages and their effects on siRNA structure, function, and interaction with RNAi proteins. Screening of these siRNAs against their corresponding mRNA targets showed that 2′-5′ linkages were well tolerated in the sense strand, but only at a few positions in the antisense strand. Extensive modification of the antisense strand minimally affected 5′-phosphorylation of the siRNA by kinases, however, it negatively affected siRNA loading into human AGO2. Modelling and molecular dynamics simulations were fully consistent with these findings. Furthermore, our studies indicated that the presence of a single 5′p-rN1-(2′-5′)-N2 unit in the antisense strand does not alter the ‘clover leaf’ bend and sugar puckers that are critical for anchoring the 5′-phosphate to Ago 2 MID domain. Importantly, 2′-5′-linkages had the added benefit of abrogating immune-stimulatory activity of siRNAs. Together, these results demonstrate that 2′-5′/3′-5′-modified siRNAs, when properly designed, can offer an efficient new class of siRNAs with diminished immune-stimulatory responses.

Funder

Natural Sciences and Engineering Research Council of Canada

Drug Development and Training Program

Canadian Institutes of Health Research

Southern Illinois University School of Medicine

CIHR

IRCC

IIT Bombay

Publisher

Oxford University Press (OUP)

Subject

Genetics

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