6mer Seed Toxicity in Viral microRNAs

Summary: MicroRNAs (miRNAs) are short double-stranded noncoding RNAs (19-23 nucleotides) that regulate gene expression by suppressing mRNAs through RNA interference. Targeting is determined by the seed sequence (position 2-7/8) of the mature miRNA. A minimal G-rich seed of just six nucleotides is hi...

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Main Authors: Andrea E. Murmann, Elizabeth T. Bartom, Matthew J. Schipma, Jacob Vilker, Siquan Chen, Marcus E. Peter
Format: Article
Language:English
Published: Elsevier 2020-02-01
Series:iScience
Online Access:http://www.sciencedirect.com/science/article/pii/S258900421930481X
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spelling doaj-d9db1aba7711450a8d10d6d04a2006762020-11-25T02:04:15ZengElsevieriScience2589-00422020-02-012326mer Seed Toxicity in Viral microRNAsAndrea E. Murmann0Elizabeth T. Bartom1Matthew J. Schipma2Jacob Vilker3Siquan Chen4Marcus E. Peter5Division Hematology/Oncology, Department of Medicine, Northwestern University, Chicago, IL 60611, USADepartment of Biochemistry and Molecular Genetics, Northwestern University, Chicago, IL 60611, USADepartment of Biochemistry and Molecular Genetics, Northwestern University, Chicago, IL 60611, USADivision Hematology/Oncology, Department of Medicine, Northwestern University, Chicago, IL 60611, USACellular Screening Center, Institute for Genomics & Systems Biology, The University of Chicago, Chicago, IL 60637, USADivision Hematology/Oncology, Department of Medicine, Northwestern University, Chicago, IL 60611, USA; Department of Biochemistry and Molecular Genetics, Northwestern University, Chicago, IL 60611, USA; Corresponding authorSummary: MicroRNAs (miRNAs) are short double-stranded noncoding RNAs (19-23 nucleotides) that regulate gene expression by suppressing mRNAs through RNA interference. Targeting is determined by the seed sequence (position 2-7/8) of the mature miRNA. A minimal G-rich seed of just six nucleotides is highly toxic to cells by targeting genes essential for cell survival. A screen of 215 miRNAs encoded by 17 human pathogenic viruses (v-miRNAs) now suggests that a number of v-miRNAs can kill cells through a G-rich 6mer sequence embedded in their seed. Specifically, we demonstrate that miR-K12-6-5p, an oncoviral mimic of the tumor suppressive miR-15/16 family encoded by human Kaposi sarcoma-associated herpes virus, harbors a noncanonical toxic 6mer seed (position 3-8) and that v-miRNAs are more likely than cellular miRNAs to utilize a noncanonical 6mer seed. Our data suggest that during evolution viruses evolved to use 6mer seed toxicity to kill cells. : Molecular Genetics; Virology; Bioinformatics Subject Areas: Molecular Genetics, Virology, Bioinformaticshttp://www.sciencedirect.com/science/article/pii/S258900421930481X
collection DOAJ
language English
format Article
sources DOAJ
author Andrea E. Murmann
Elizabeth T. Bartom
Matthew J. Schipma
Jacob Vilker
Siquan Chen
Marcus E. Peter
spellingShingle Andrea E. Murmann
Elizabeth T. Bartom
Matthew J. Schipma
Jacob Vilker
Siquan Chen
Marcus E. Peter
6mer Seed Toxicity in Viral microRNAs
iScience
author_facet Andrea E. Murmann
Elizabeth T. Bartom
Matthew J. Schipma
Jacob Vilker
Siquan Chen
Marcus E. Peter
author_sort Andrea E. Murmann
title 6mer Seed Toxicity in Viral microRNAs
title_short 6mer Seed Toxicity in Viral microRNAs
title_full 6mer Seed Toxicity in Viral microRNAs
title_fullStr 6mer Seed Toxicity in Viral microRNAs
title_full_unstemmed 6mer Seed Toxicity in Viral microRNAs
title_sort 6mer seed toxicity in viral micrornas
publisher Elsevier
series iScience
issn 2589-0042
publishDate 2020-02-01
description Summary: MicroRNAs (miRNAs) are short double-stranded noncoding RNAs (19-23 nucleotides) that regulate gene expression by suppressing mRNAs through RNA interference. Targeting is determined by the seed sequence (position 2-7/8) of the mature miRNA. A minimal G-rich seed of just six nucleotides is highly toxic to cells by targeting genes essential for cell survival. A screen of 215 miRNAs encoded by 17 human pathogenic viruses (v-miRNAs) now suggests that a number of v-miRNAs can kill cells through a G-rich 6mer sequence embedded in their seed. Specifically, we demonstrate that miR-K12-6-5p, an oncoviral mimic of the tumor suppressive miR-15/16 family encoded by human Kaposi sarcoma-associated herpes virus, harbors a noncanonical toxic 6mer seed (position 3-8) and that v-miRNAs are more likely than cellular miRNAs to utilize a noncanonical 6mer seed. Our data suggest that during evolution viruses evolved to use 6mer seed toxicity to kill cells. : Molecular Genetics; Virology; Bioinformatics Subject Areas: Molecular Genetics, Virology, Bioinformatics
url http://www.sciencedirect.com/science/article/pii/S258900421930481X
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