The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs

ABSTRACT Viruses utilize several strategies to cause latent infection and evade host immune responses. Long non-coding RNA (lncRNA), a class of non-protein-encoding RNA that regulates various cellular functions by interacting with RNA-binding proteins, plays important roles for viral latency in seve...

Full description

Bibliographic Details
Main Authors: Kiyohiko Andoh, Asami Nishimori, Yuichi Matsuura
Format: Article
Language:English
Published: American Society for Microbiology 2023-10-01
Series:Microbiology Spectrum
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/spectrum.00855-23
_version_ 1827792053701967872
author Kiyohiko Andoh
Asami Nishimori
Yuichi Matsuura
author_facet Kiyohiko Andoh
Asami Nishimori
Yuichi Matsuura
author_sort Kiyohiko Andoh
collection DOAJ
description ABSTRACT Viruses utilize several strategies to cause latent infection and evade host immune responses. Long non-coding RNA (lncRNA), a class of non-protein-encoding RNA that regulates various cellular functions by interacting with RNA-binding proteins, plays important roles for viral latency in several viruses, such as herpesviruses and retroviruses, due to its lack of antigenicity. Bovine leukemia virus (BLV), which belongs to the family Retroviridae, encodes the BLV-derived lncRNA AS1-S, which is a major transcript expressed in latently infected cells. We herein identified bovine heterogeneous nuclear ribonucleoprotein M (hnRNPM), an RNA-binding protein located in the nucleus, as the binding partner of AS1-S using an RNA-protein pull-down assay. The pull-down assay using recombinant hnRNPM mutants showed that RNA recognition motifs (RRMs) 1 and 2, located in the N-terminal region of bovine hnRNPM, were responsible for the binding to AS1-S. Furthermore, RNA immunoprecipitation (RIP) assay results showed that the expression of AS1-S increased the number of mRNAs that co-immunoprecipitated with bovine hnRNPM in MDBK cells. These results suggested that AS1-S could alter the interaction between hnRNPM and host mRNAs, potentially interfering with cellular functions during the initial phase of mRNA maturation in the nucleus. Since most of the identified mRNAs that exhibited increased binding to hnRNPM were correlated with the KEGG term “Pathways in cancer,” AS1-S might affect the proliferation and expansion of BLV-infected cells and contribute to tumor progression. IMPORTANCE BLV infects bovine B cells and causes malignant lymphoma, a disease that greatly affects the livestock industry. Due to its low incidence and long latent period, the molecular mechanisms underlying the progression of lymphoma remain enigmatic. Several non-coding RNAs (ncRNAs), such as miRNA and lncRNA, have recently been discovered in the BLV genome, and the relationship between BLV pathogenesis and these ncRNAs is attracting attention. However, most of the molecular functions of these transcripts remain unidentified. To the best of our knowledge, this is the first report describing a molecular function for the BLV-derived lncRNA AS1-S. The findings reported herein reveal a novel mechanism underlying BLV pathogenesis that could provide important insights for not only BLV research but also comparative studies of retroviruses.
first_indexed 2024-03-11T17:55:22Z
format Article
id doaj.art-b5df1a45b5b94d6ab12b88336c5a3013
institution Directory Open Access Journal
issn 2165-0497
language English
last_indexed 2024-03-11T17:55:22Z
publishDate 2023-10-01
publisher American Society for Microbiology
record_format Article
series Microbiology Spectrum
spelling doaj.art-b5df1a45b5b94d6ab12b88336c5a30132023-10-17T13:04:36ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972023-10-0111510.1128/spectrum.00855-23The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAsKiyohiko Andoh0Asami Nishimori1Yuichi Matsuura2National Institute of Animal Health, National Agriculture and Food Research Organization , Tsukuba, Ibaraki, JapanNational Institute of Animal Health, National Agriculture and Food Research Organization , Tsukuba, Ibaraki, JapanNational Institute of Animal Health, National Agriculture and Food Research Organization , Tsukuba, Ibaraki, JapanABSTRACT Viruses utilize several strategies to cause latent infection and evade host immune responses. Long non-coding RNA (lncRNA), a class of non-protein-encoding RNA that regulates various cellular functions by interacting with RNA-binding proteins, plays important roles for viral latency in several viruses, such as herpesviruses and retroviruses, due to its lack of antigenicity. Bovine leukemia virus (BLV), which belongs to the family Retroviridae, encodes the BLV-derived lncRNA AS1-S, which is a major transcript expressed in latently infected cells. We herein identified bovine heterogeneous nuclear ribonucleoprotein M (hnRNPM), an RNA-binding protein located in the nucleus, as the binding partner of AS1-S using an RNA-protein pull-down assay. The pull-down assay using recombinant hnRNPM mutants showed that RNA recognition motifs (RRMs) 1 and 2, located in the N-terminal region of bovine hnRNPM, were responsible for the binding to AS1-S. Furthermore, RNA immunoprecipitation (RIP) assay results showed that the expression of AS1-S increased the number of mRNAs that co-immunoprecipitated with bovine hnRNPM in MDBK cells. These results suggested that AS1-S could alter the interaction between hnRNPM and host mRNAs, potentially interfering with cellular functions during the initial phase of mRNA maturation in the nucleus. Since most of the identified mRNAs that exhibited increased binding to hnRNPM were correlated with the KEGG term “Pathways in cancer,” AS1-S might affect the proliferation and expansion of BLV-infected cells and contribute to tumor progression. IMPORTANCE BLV infects bovine B cells and causes malignant lymphoma, a disease that greatly affects the livestock industry. Due to its low incidence and long latent period, the molecular mechanisms underlying the progression of lymphoma remain enigmatic. Several non-coding RNAs (ncRNAs), such as miRNA and lncRNA, have recently been discovered in the BLV genome, and the relationship between BLV pathogenesis and these ncRNAs is attracting attention. However, most of the molecular functions of these transcripts remain unidentified. To the best of our knowledge, this is the first report describing a molecular function for the BLV-derived lncRNA AS1-S. The findings reported herein reveal a novel mechanism underlying BLV pathogenesis that could provide important insights for not only BLV research but also comparative studies of retroviruses.https://journals.asm.org/doi/10.1128/spectrum.00855-23AS1-Sbovine leukemia virushnRNPMlymphomanon-coding RNA
spellingShingle Kiyohiko Andoh
Asami Nishimori
Yuichi Matsuura
The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs
Microbiology Spectrum
AS1-S
bovine leukemia virus
hnRNPM
lymphoma
non-coding RNA
title The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs
title_full The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs
title_fullStr The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs
title_full_unstemmed The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs
title_short The bovine leukemia virus-derived long non-coding RNA AS1-S binds to bovine hnRNPM and alters the interaction between hnRNPM and host mRNAs
title_sort bovine leukemia virus derived long non coding rna as1 s binds to bovine hnrnpm and alters the interaction between hnrnpm and host mrnas
topic AS1-S
bovine leukemia virus
hnRNPM
lymphoma
non-coding RNA
url https://journals.asm.org/doi/10.1128/spectrum.00855-23
work_keys_str_mv AT kiyohikoandoh thebovineleukemiavirusderivedlongnoncodingrnaas1sbindstobovinehnrnpmandalterstheinteractionbetweenhnrnpmandhostmrnas
AT asaminishimori thebovineleukemiavirusderivedlongnoncodingrnaas1sbindstobovinehnrnpmandalterstheinteractionbetweenhnrnpmandhostmrnas
AT yuichimatsuura thebovineleukemiavirusderivedlongnoncodingrnaas1sbindstobovinehnrnpmandalterstheinteractionbetweenhnrnpmandhostmrnas
AT kiyohikoandoh bovineleukemiavirusderivedlongnoncodingrnaas1sbindstobovinehnrnpmandalterstheinteractionbetweenhnrnpmandhostmrnas
AT asaminishimori bovineleukemiavirusderivedlongnoncodingrnaas1sbindstobovinehnrnpmandalterstheinteractionbetweenhnrnpmandhostmrnas
AT yuichimatsuura bovineleukemiavirusderivedlongnoncodingrnaas1sbindstobovinehnrnpmandalterstheinteractionbetweenhnrnpmandhostmrnas