Sequence complementarity between human noncoding RNAs and SARS-CoV-2 genes: What are the implications for human health?
To investigate in silico the presence of nucleotide sequence complementarity between the RNA genome of Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) and human non-coding (nc)RNA genes. The FASTA sequence (NC_045512.2) of each of the 11 SARS-CoV-2 isolate Wuhan-Hu-1 genes was retrieved...
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description | To investigate in silico the presence of nucleotide sequence complementarity between the RNA genome of Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) and human non-coding (nc)RNA genes.
The FASTA sequence (NC_045512.2) of each of the 11 SARS-CoV-2 isolate Wuhan-Hu-1 genes was retrieved from NCBI.nlm.nih.gov/gene and the Ensembl.org library interrogated for any base-pair match with human ncRNA genes. SARS-CoV-2 gene-matched human ncRNAs were screened for functional activity using bioinformatic analysis. Finally, associations between identified ncRNAs and human diseases were searched in GWAS databases.
A total of 252 matches were found between the nucleotide sequence of SARS-CoV-2 genes and human ncRNAs. With the exception of two small nuclear RNAs, all of them were long non-coding (lnc)RNAs expressed mainly in testis and central nervous system under physiological conditions. The percentage of alignment ranged from 91.30% to 100% with a mean nucleotide alignment length of 17.5 ± 2.4. Thirty-three (13.09%) of them contained predicted R-loop forming sequences, but none of these intersected the complementary sequences of SARS-CoV-2. However, in 31 cases matches fell on ncRNA regulatory sites, whose adjacent coding genes are mostly involved in cancer, immunological and neurological pathways. Similarly, several polymorphic variants of detected non-coding genes have been associated with neuropsychiatric and proliferative disorders.
This pivotal in silico study shows that SARS-CoV-2 genes have Watson-Crick nucleotide complementarity to human ncRNA sequences, potentially disrupting ncRNA epigenetic control of target genes. It remains to be elucidated whether this could result in the development of human disease in the long term.
•Viruses may establish an epigenetic crosstalk with human ncRNAs.•SARS-CoV-2 genes overlap with the transcripts of 130 human lncRNAs and 2 snRNAs.•Detected human ncRNAs may be involved in cancer and autoimmune pathways.•Such a nucleotide interaction may be at the basis of COVID-19 complications. |
doi_str_mv | 10.1016/j.bbadis.2021.166291 |
format | Article |
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The FASTA sequence (NC_045512.2) of each of the 11 SARS-CoV-2 isolate Wuhan-Hu-1 genes was retrieved from NCBI.nlm.nih.gov/gene and the Ensembl.org library interrogated for any base-pair match with human ncRNA genes. SARS-CoV-2 gene-matched human ncRNAs were screened for functional activity using bioinformatic analysis. Finally, associations between identified ncRNAs and human diseases were searched in GWAS databases.
A total of 252 matches were found between the nucleotide sequence of SARS-CoV-2 genes and human ncRNAs. With the exception of two small nuclear RNAs, all of them were long non-coding (lnc)RNAs expressed mainly in testis and central nervous system under physiological conditions. The percentage of alignment ranged from 91.30% to 100% with a mean nucleotide alignment length of 17.5 ± 2.4. Thirty-three (13.09%) of them contained predicted R-loop forming sequences, but none of these intersected the complementary sequences of SARS-CoV-2. However, in 31 cases matches fell on ncRNA regulatory sites, whose adjacent coding genes are mostly involved in cancer, immunological and neurological pathways. Similarly, several polymorphic variants of detected non-coding genes have been associated with neuropsychiatric and proliferative disorders.
This pivotal in silico study shows that SARS-CoV-2 genes have Watson-Crick nucleotide complementarity to human ncRNA sequences, potentially disrupting ncRNA epigenetic control of target genes. It remains to be elucidated whether this could result in the development of human disease in the long term.
•Viruses may establish an epigenetic crosstalk with human ncRNAs.•SARS-CoV-2 genes overlap with the transcripts of 130 human lncRNAs and 2 snRNAs.•Detected human ncRNAs may be involved in cancer and autoimmune pathways.•Such a nucleotide interaction may be at the basis of COVID-19 complications.</description><identifier>ISSN: 0925-4439</identifier><identifier>EISSN: 1879-260X</identifier><identifier>DOI: 10.1016/j.bbadis.2021.166291</identifier><identifier>PMID: 34662705</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Base Sequence ; Bioinformatics ; COVID-19 ; COVID-19 - genetics ; COVID-19 - virology ; Epigenesis, Genetic ; Epigenetics ; Genes, Viral ; Humans ; Long non-coding RNA ; Neoplasms - genetics ; RNA, Long Noncoding - genetics ; RNA, Untranslated - genetics ; SARS-CoV-2 ; SARS-CoV-2 - genetics ; Sequence Alignment ; Sequence Homology, Nucleic Acid ; Small nuclear RNA</subject><ispartof>Biochimica et biophysica acta. Molecular basis of disease, 2022-02, Vol.1868 (2), p.166291-166291, Article 166291</ispartof><rights>2021</rights><rights>Copyright © 2021. Published by Elsevier B.V.</rights><rights>2021 Published by Elsevier B.V. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-a82c7cba85a6c6485b38f6fef7eec14b1e4e60fc01c1537ffac58215fdb3a6e63</citedby><cites>FETCH-LOGICAL-c463t-a82c7cba85a6c6485b38f6fef7eec14b1e4e60fc01c1537ffac58215fdb3a6e63</cites><orcidid>0000-0001-8426-1395</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbadis.2021.166291$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34662705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Talotta, Rossella</creatorcontrib><creatorcontrib>Bahrami, Shervin</creatorcontrib><creatorcontrib>Laska, Magdalena Janina</creatorcontrib><title>Sequence complementarity between human noncoding RNAs and SARS-CoV-2 genes: What are the implications for human health?</title><title>Biochimica et biophysica acta. Molecular basis of disease</title><addtitle>Biochim Biophys Acta Mol Basis Dis</addtitle><description>To investigate in silico the presence of nucleotide sequence complementarity between the RNA genome of Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) and human non-coding (nc)RNA genes.
The FASTA sequence (NC_045512.2) of each of the 11 SARS-CoV-2 isolate Wuhan-Hu-1 genes was retrieved from NCBI.nlm.nih.gov/gene and the Ensembl.org library interrogated for any base-pair match with human ncRNA genes. SARS-CoV-2 gene-matched human ncRNAs were screened for functional activity using bioinformatic analysis. Finally, associations between identified ncRNAs and human diseases were searched in GWAS databases.
A total of 252 matches were found between the nucleotide sequence of SARS-CoV-2 genes and human ncRNAs. With the exception of two small nuclear RNAs, all of them were long non-coding (lnc)RNAs expressed mainly in testis and central nervous system under physiological conditions. The percentage of alignment ranged from 91.30% to 100% with a mean nucleotide alignment length of 17.5 ± 2.4. Thirty-three (13.09%) of them contained predicted R-loop forming sequences, but none of these intersected the complementary sequences of SARS-CoV-2. However, in 31 cases matches fell on ncRNA regulatory sites, whose adjacent coding genes are mostly involved in cancer, immunological and neurological pathways. Similarly, several polymorphic variants of detected non-coding genes have been associated with neuropsychiatric and proliferative disorders.
This pivotal in silico study shows that SARS-CoV-2 genes have Watson-Crick nucleotide complementarity to human ncRNA sequences, potentially disrupting ncRNA epigenetic control of target genes. It remains to be elucidated whether this could result in the development of human disease in the long term.
•Viruses may establish an epigenetic crosstalk with human ncRNAs.•SARS-CoV-2 genes overlap with the transcripts of 130 human lncRNAs and 2 snRNAs.•Detected human ncRNAs may be involved in cancer and autoimmune pathways.•Such a nucleotide interaction may be at the basis of COVID-19 complications.</description><subject>Base Sequence</subject><subject>Bioinformatics</subject><subject>COVID-19</subject><subject>COVID-19 - genetics</subject><subject>COVID-19 - virology</subject><subject>Epigenesis, Genetic</subject><subject>Epigenetics</subject><subject>Genes, Viral</subject><subject>Humans</subject><subject>Long non-coding RNA</subject><subject>Neoplasms - genetics</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Untranslated - genetics</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 - genetics</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Small nuclear RNA</subject><issn>0925-4439</issn><issn>1879-260X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1vEzEQhi0EomnhHyDkI5cN_lh7NxxAUQQFqQKp4etmeb3jrKNdO7WdVv33OEoocGEuPsw773jeB6EXlMwpofL1dt51undpzgijcyolW9BHaEbbZlExSX4-RjOyYKKqa744Q-cpbUkp2ZCn6IzXRd4QMUN3a7jZgzeATZh2I0zgs44u3-MO8h2Ax8N-0h774E3ond_g68_LhLXv8Xp5va5W4XvF8AY8pDf4x6Az1hFwHgC7YueMzi74hG2IJ6MB9JiHd8_QE6vHBM9P7wX69uH919XH6urL5afV8qoyteS50i0zjel0K7Q0sm5Fx1srLdgGwNC6o1CDJNYQaqjgjbXaiJZRYfuOawmSX6C3R9_dvpugN-W8qEe1i27S8V4F7dS_He8GtQm3qhW0pVwUg1cngxhKUimrySUD46g9hH1STLS8RMxqXqT1UWpiSCmCfVhDiTowU1t1ZKYOzNSRWRl7-fcXH4Z-Q_pzA5Sgbh1ElYw7MOtdBJNVH9z_N_wCzuKsbw</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Talotta, Rossella</creator><creator>Bahrami, Shervin</creator><creator>Laska, Magdalena Janina</creator><general>Elsevier B.V</general><general>Published by Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8426-1395</orcidid></search><sort><creationdate>20220201</creationdate><title>Sequence complementarity between human noncoding RNAs and SARS-CoV-2 genes: What are the implications for human health?</title><author>Talotta, Rossella ; Bahrami, Shervin ; Laska, Magdalena Janina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-a82c7cba85a6c6485b38f6fef7eec14b1e4e60fc01c1537ffac58215fdb3a6e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Base Sequence</topic><topic>Bioinformatics</topic><topic>COVID-19</topic><topic>COVID-19 - genetics</topic><topic>COVID-19 - virology</topic><topic>Epigenesis, Genetic</topic><topic>Epigenetics</topic><topic>Genes, Viral</topic><topic>Humans</topic><topic>Long non-coding RNA</topic><topic>Neoplasms - genetics</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Untranslated - genetics</topic><topic>SARS-CoV-2</topic><topic>SARS-CoV-2 - genetics</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Small nuclear RNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Talotta, Rossella</creatorcontrib><creatorcontrib>Bahrami, Shervin</creatorcontrib><creatorcontrib>Laska, Magdalena Janina</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochimica et biophysica acta. Molecular basis of disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Talotta, Rossella</au><au>Bahrami, Shervin</au><au>Laska, Magdalena Janina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequence complementarity between human noncoding RNAs and SARS-CoV-2 genes: What are the implications for human health?</atitle><jtitle>Biochimica et biophysica acta. Molecular basis of disease</jtitle><addtitle>Biochim Biophys Acta Mol Basis Dis</addtitle><date>2022-02-01</date><risdate>2022</risdate><volume>1868</volume><issue>2</issue><spage>166291</spage><epage>166291</epage><pages>166291-166291</pages><artnum>166291</artnum><issn>0925-4439</issn><eissn>1879-260X</eissn><abstract>To investigate in silico the presence of nucleotide sequence complementarity between the RNA genome of Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) and human non-coding (nc)RNA genes.
The FASTA sequence (NC_045512.2) of each of the 11 SARS-CoV-2 isolate Wuhan-Hu-1 genes was retrieved from NCBI.nlm.nih.gov/gene and the Ensembl.org library interrogated for any base-pair match with human ncRNA genes. SARS-CoV-2 gene-matched human ncRNAs were screened for functional activity using bioinformatic analysis. Finally, associations between identified ncRNAs and human diseases were searched in GWAS databases.
A total of 252 matches were found between the nucleotide sequence of SARS-CoV-2 genes and human ncRNAs. With the exception of two small nuclear RNAs, all of them were long non-coding (lnc)RNAs expressed mainly in testis and central nervous system under physiological conditions. The percentage of alignment ranged from 91.30% to 100% with a mean nucleotide alignment length of 17.5 ± 2.4. Thirty-three (13.09%) of them contained predicted R-loop forming sequences, but none of these intersected the complementary sequences of SARS-CoV-2. However, in 31 cases matches fell on ncRNA regulatory sites, whose adjacent coding genes are mostly involved in cancer, immunological and neurological pathways. Similarly, several polymorphic variants of detected non-coding genes have been associated with neuropsychiatric and proliferative disorders.
This pivotal in silico study shows that SARS-CoV-2 genes have Watson-Crick nucleotide complementarity to human ncRNA sequences, potentially disrupting ncRNA epigenetic control of target genes. It remains to be elucidated whether this could result in the development of human disease in the long term.
•Viruses may establish an epigenetic crosstalk with human ncRNAs.•SARS-CoV-2 genes overlap with the transcripts of 130 human lncRNAs and 2 snRNAs.•Detected human ncRNAs may be involved in cancer and autoimmune pathways.•Such a nucleotide interaction may be at the basis of COVID-19 complications.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34662705</pmid><doi>10.1016/j.bbadis.2021.166291</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8426-1395</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence Bioinformatics COVID-19 COVID-19 - genetics COVID-19 - virology Epigenesis, Genetic Epigenetics Genes, Viral Humans Long non-coding RNA Neoplasms - genetics RNA, Long Noncoding - genetics RNA, Untranslated - genetics SARS-CoV-2 SARS-CoV-2 - genetics Sequence Alignment Sequence Homology, Nucleic Acid Small nuclear RNA |
title | Sequence complementarity between human noncoding RNAs and SARS-CoV-2 genes: What are the implications for human health? |
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