Skip to main content
Top
Published in: Archives of Virology 11/2010

01-11-2010 | Original Article

Marek’s disease virus microRNA designated Mdv1-pre-miR-M4 targets both cellular and viral genes

Authors: Benoît Muylkens, Damien Coupeau, Ginette Dambrine, Sascha Trapp, Denis Rasschaert

Published in: Archives of Virology | Issue 11/2010

Login to get access

Abstract

Mdv1-miR-M4 is one of 25 microRNAs (miRNAs) expressed by Marek’s disease virus (MDV-1), an oncogenic alphaherpesvirus that induces fatal T-cell lymphoma in chickens. Mdv1-miR-M4 was shown to be the second functional viral ortholog of miR-155, a cellular miRNA that plays a crucial role in several physiological and pathological processes in lymphocyte biology. In this study, we investigated a panel of putative mdv1-miR-M4 targets involved in gene networks affecting both cellular and viral life cycles. Using luciferase reporter assays, we showed that mdv1-miR-M4-5P and miR-155 efficiently targeted a common set of 3′ untranslated regions (3′UTR) of six cellular genes (GPM6B, RREB1, c-Myb, MAP3K7IP2, PU.1 and C/EBP). In addition, we also investigated the interactions between mdv1-miR-M4-5P and mdv1-miR-M43P and viral mRNAs encoding UL28 and UL32 in both reporter and western blot assays. Mdv1-miR-M4 specifically inhibited the translation of these two viral proteins, which are involved in the cleavage/packaging of herpesvirus DNA.
Appendix
Available only for authorised users
Literature
1.
go back to reference Pfeffer S, Zavolan M, Grasser FA, Chien M, Russo JJ, Ju J, John B, Enright AJ, Marks D, Sander C, Tuschl T (2004) Identification of virus-encoded micrornas. Science 304(5671):734–736CrossRefPubMed Pfeffer S, Zavolan M, Grasser FA, Chien M, Russo JJ, Ju J, John B, Enright AJ, Marks D, Sander C, Tuschl T (2004) Identification of virus-encoded micrornas. Science 304(5671):734–736CrossRefPubMed
2.
go back to reference Pfeffer S, Sewer A, Lagos-Quintana M, Sheridan R, Sander C, Grasser FA, van Dyk LF, Ho CK, Shuman S, Chien M, Russo JJ, Ju J, Randall G, Lindenbach BD, Rice CM, Simon V, Ho DD, Zavolan M, Tuschl T (2005) Identification of micrornas of the herpesvirus family. Nat Methods 2(4):269–276CrossRefPubMed Pfeffer S, Sewer A, Lagos-Quintana M, Sheridan R, Sander C, Grasser FA, van Dyk LF, Ho CK, Shuman S, Chien M, Russo JJ, Ju J, Randall G, Lindenbach BD, Rice CM, Simon V, Ho DD, Zavolan M, Tuschl T (2005) Identification of micrornas of the herpesvirus family. Nat Methods 2(4):269–276CrossRefPubMed
3.
go back to reference Gottwein E, Cullen BR (2008) Viral and cellular micrornas as determinants of viral pathogenesis and immunity. Cell Host Microbe 3(6):375–387CrossRefPubMed Gottwein E, Cullen BR (2008) Viral and cellular micrornas as determinants of viral pathogenesis and immunity. Cell Host Microbe 3(6):375–387CrossRefPubMed
4.
go back to reference Boss IW, Plaisance KB, Renne R (2009) Role of virus-encoded micrornas in herpesvirus biology. Trends Microbiol 17(12):544–553CrossRefPubMed Boss IW, Plaisance KB, Renne R (2009) Role of virus-encoded micrornas in herpesvirus biology. Trends Microbiol 17(12):544–553CrossRefPubMed
5.
go back to reference Burnside J, Bernberg E, Anderson A, Lu C, Meyers BC, Green PJ, Jain N, Isaacs G, Morgan RW (2006) Marek’s disease virus encodes micrornas that map to meq and the latency-associated transcript. J Virol 80(17):8778–8786CrossRefPubMed Burnside J, Bernberg E, Anderson A, Lu C, Meyers BC, Green PJ, Jain N, Isaacs G, Morgan RW (2006) Marek’s disease virus encodes micrornas that map to meq and the latency-associated transcript. J Virol 80(17):8778–8786CrossRefPubMed
6.
go back to reference Burnside J, Morgan RW (2007) Genomics and marek’s disease virus. Cytogenet Genome Res 117(1–4):376–387CrossRefPubMed Burnside J, Morgan RW (2007) Genomics and marek’s disease virus. Cytogenet Genome Res 117(1–4):376–387CrossRefPubMed
7.
go back to reference Burnside J, Ouyang M, Anderson A, Bernberg E, Lu C, Meyers BC, Green PJ, Markis M, Isaacs G, Huang E, Morgan RW (2008) Deep sequencing of chicken micrornas. BMC Genomics 9:185CrossRefPubMed Burnside J, Ouyang M, Anderson A, Bernberg E, Lu C, Meyers BC, Green PJ, Markis M, Isaacs G, Huang E, Morgan RW (2008) Deep sequencing of chicken micrornas. BMC Genomics 9:185CrossRefPubMed
8.
go back to reference Morgan R, Anderson A, Bernberg E, Kamboj S, Huang E, Lagasse G, Isaacs G, Parcells M, Meyers BC, Green PJ, Burnside J (2008) Sequence conservation and differential expression of marek’s disease virus micrornas. J Virol 82(24):12213–12220CrossRefPubMed Morgan R, Anderson A, Bernberg E, Kamboj S, Huang E, Lagasse G, Isaacs G, Parcells M, Meyers BC, Green PJ, Burnside J (2008) Sequence conservation and differential expression of marek’s disease virus micrornas. J Virol 82(24):12213–12220CrossRefPubMed
9.
go back to reference Yao Y, Zhao Y, Xu H, Smith LP, Lawrie CH, Watson M, Nair V (2008) Microrna profile of marek’s disease virus-transformed t-cell line msb-1: predominance of virus-encoded micrornas. J Virol 82(8):4007–4015CrossRefPubMed Yao Y, Zhao Y, Xu H, Smith LP, Lawrie CH, Watson M, Nair V (2008) Microrna profile of marek’s disease virus-transformed t-cell line msb-1: predominance of virus-encoded micrornas. J Virol 82(8):4007–4015CrossRefPubMed
10.
go back to reference Areste C, Blackbourn DJ (2009) Modulation of the immune system by kaposi’s sarcoma-associated herpesvirus. Trends Microbiol 17(3):119–129CrossRefPubMed Areste C, Blackbourn DJ (2009) Modulation of the immune system by kaposi’s sarcoma-associated herpesvirus. Trends Microbiol 17(3):119–129CrossRefPubMed
11.
go back to reference Barth S, Pfuhl T, Mamiani A, Ehses C, Roemer K, Kremmer E, Jaker C, Hock J, Meister G, Grasser FA (2008) Epstein-barr virus-encoded microrna mir-bart2 down-regulates the viral DNA polymerase balf5. Nucleic Acids Res 36(2):666–675CrossRefPubMed Barth S, Pfuhl T, Mamiani A, Ehses C, Roemer K, Kremmer E, Jaker C, Hock J, Meister G, Grasser FA (2008) Epstein-barr virus-encoded microrna mir-bart2 down-regulates the viral DNA polymerase balf5. Nucleic Acids Res 36(2):666–675CrossRefPubMed
12.
go back to reference Stern-Ginossar N, Saleh N, Goldberg MD, Prichard M, Wolf DG, Mandelboim O (2009) Analysis of human cytomegalovirus-encoded microrna activity during infection. J Virol 83(20):10684–10693CrossRefPubMed Stern-Ginossar N, Saleh N, Goldberg MD, Prichard M, Wolf DG, Mandelboim O (2009) Analysis of human cytomegalovirus-encoded microrna activity during infection. J Virol 83(20):10684–10693CrossRefPubMed
13.
go back to reference Stern-Ginossar N, Elefant N, Zimmermann A, Wolf DG, Saleh N, Biton M, Horwitz E, Prokocimer Z, Prichard M, Hahn G, Goldman-Wohl D, Greenfield C, Yagel S, Hengel H, Altuvia Y, Margalit H, Mandelboim O (2007) Host immune system gene targeting by a viral mirna. Science 317(5836):376–381CrossRefPubMed Stern-Ginossar N, Elefant N, Zimmermann A, Wolf DG, Saleh N, Biton M, Horwitz E, Prokocimer Z, Prichard M, Hahn G, Goldman-Wohl D, Greenfield C, Yagel S, Hengel H, Altuvia Y, Margalit H, Mandelboim O (2007) Host immune system gene targeting by a viral mirna. Science 317(5836):376–381CrossRefPubMed
14.
go back to reference Xia T, O’Hara A, Araujo I, Barreto J, Carvalho E, Sapucaia JB, Ramos JC, Luz E, Pedroso C, Manrique M, Toomey NL, Brites C, Dittmer DP, Harrington WJ Jr (2008) Ebv micrornas in primary lymphomas and targeting of cxcl-11 by ebv-mir-bhrf1-3. Cancer Res 68(5):1436–1442CrossRefPubMed Xia T, O’Hara A, Araujo I, Barreto J, Carvalho E, Sapucaia JB, Ramos JC, Luz E, Pedroso C, Manrique M, Toomey NL, Brites C, Dittmer DP, Harrington WJ Jr (2008) Ebv micrornas in primary lymphomas and targeting of cxcl-11 by ebv-mir-bhrf1-3. Cancer Res 68(5):1436–1442CrossRefPubMed
15.
go back to reference Choy EY, Siu KL, Kok KH, Lung RW, Tsang CM, To KF, Kwong DL, Tsao SW, Jin DY (2008) An epstein-barr virus-encoded microrna targets puma to promote host cell survival. J Exp Med 205(11):2551–2560CrossRefPubMed Choy EY, Siu KL, Kok KH, Lung RW, Tsang CM, To KF, Kwong DL, Tsao SW, Jin DY (2008) An epstein-barr virus-encoded microrna targets puma to promote host cell survival. J Exp Med 205(11):2551–2560CrossRefPubMed
16.
go back to reference Samols MA, Skalsky RL, Maldonado AM, Riva A, Lopez MC, Baker HV, Renne R (2007) Identification of cellular genes targeted by kshv-encoded micrornas. PLoS Pathog 3(5):e65CrossRefPubMed Samols MA, Skalsky RL, Maldonado AM, Riva A, Lopez MC, Baker HV, Renne R (2007) Identification of cellular genes targeted by kshv-encoded micrornas. PLoS Pathog 3(5):e65CrossRefPubMed
17.
go back to reference Skalsky RL, Samols MA, Plaisance KB, Boss IW, Riva A, Lopez MC, Baker HV, Renne R (2007) Kaposi’s sarcoma-associated herpesvirus encodes an ortholog of mir-155. J Virol 81(23):12836–12845CrossRefPubMed Skalsky RL, Samols MA, Plaisance KB, Boss IW, Riva A, Lopez MC, Baker HV, Renne R (2007) Kaposi’s sarcoma-associated herpesvirus encodes an ortholog of mir-155. J Virol 81(23):12836–12845CrossRefPubMed
18.
go back to reference Gottwein E, Mukherjee N, Sachse C, Frenzel C, Majoros WH, Chi JT, Braich R, Manoharan M, Soutschek J, Ohler U, Cullen BR (2007) A viral microrna functions as an orthologue of cellular mir-155. Nature 450(7172):1096–1099CrossRefPubMed Gottwein E, Mukherjee N, Sachse C, Frenzel C, Majoros WH, Chi JT, Braich R, Manoharan M, Soutschek J, Ohler U, Cullen BR (2007) A viral microrna functions as an orthologue of cellular mir-155. Nature 450(7172):1096–1099CrossRefPubMed
19.
go back to reference Zhao Y, Yao Y, Xu H, Lambeth L, Smith LP, Kgosana L, Wang X, Nair V (2009) A functional microrna-155 ortholog encoded by the oncogenic marek’s disease virus. J Virol 83(1):489–492CrossRefPubMed Zhao Y, Yao Y, Xu H, Lambeth L, Smith LP, Kgosana L, Wang X, Nair V (2009) A functional microrna-155 ortholog encoded by the oncogenic marek’s disease virus. J Virol 83(1):489–492CrossRefPubMed
20.
go back to reference Tili E, Croce CM, Michaille JJ (2009) Mir-155: on the crosstalk between inflammation and cancer. Int Rev Immunol 28(5):264–284CrossRefPubMed Tili E, Croce CM, Michaille JJ (2009) Mir-155: on the crosstalk between inflammation and cancer. Int Rev Immunol 28(5):264–284CrossRefPubMed
21.
go back to reference Faraoni I, Antonetti FR, Cardone J, Bonmassar E (2009) Mir-155 gene: a typical multifunctional microrna. Biochim Biophys Acta Faraoni I, Antonetti FR, Cardone J, Bonmassar E (2009) Mir-155 gene: a typical multifunctional microrna. Biochim Biophys Acta
22.
go back to reference Teng G, Papavasiliou FN (2008) Shhh! silencing by microrna-155. Philos Trans R Soc Lond B Biol Sci 364(1517):631–637 Teng G, Papavasiliou FN (2008) Shhh! silencing by microrna-155. Philos Trans R Soc Lond B Biol Sci 364(1517):631–637
23.
go back to reference Pichler K, Schneider G, Grassmann R (2008) Microrna mir-146a and further oncogenesis-related cellular micrornas are dysregulated in htlv-1-transformed t lymphocytes. Retrovirology 5:100CrossRefPubMed Pichler K, Schneider G, Grassmann R (2008) Microrna mir-146a and further oncogenesis-related cellular micrornas are dysregulated in htlv-1-transformed t lymphocytes. Retrovirology 5:100CrossRefPubMed
24.
go back to reference Bolisetty MT, Dy G, Tam W, Beemon KL (2009) Reticuloendotheliosis virus strain t induces mir-155, which targets jarid2 and promotes cell survival. J Virol 83(23):12009–12017CrossRefPubMed Bolisetty MT, Dy G, Tam W, Beemon KL (2009) Reticuloendotheliosis virus strain t induces mir-155, which targets jarid2 and promotes cell survival. J Virol 83(23):12009–12017CrossRefPubMed
25.
go back to reference Lu F, Weidmer A, Liu CG, Volinia S, Croce CM, Lieberman PM (2008) Epstein-barr virus-induced mir-155 attenuates nf-kappab signaling and stabilizes latent virus persistence. J Virol 82(21):10436–10443CrossRefPubMed Lu F, Weidmer A, Liu CG, Volinia S, Croce CM, Lieberman PM (2008) Epstein-barr virus-induced mir-155 attenuates nf-kappab signaling and stabilizes latent virus persistence. J Virol 82(21):10436–10443CrossRefPubMed
27.
go back to reference Yao Y, Zhao Y, Smith LP, Lawrie CH, Saunders NJ, Watson M, Nair V (2009) Differential expression of micrornas in marek’s disease virus-transformed t-lymphoma cell lines. J Gen Virol 90(Pt 7):1551–1559CrossRefPubMed Yao Y, Zhao Y, Smith LP, Lawrie CH, Saunders NJ, Watson M, Nair V (2009) Differential expression of micrornas in marek’s disease virus-transformed t-lymphoma cell lines. J Gen Virol 90(Pt 7):1551–1559CrossRefPubMed
29.
go back to reference Tam W, Ben-Yehuda D, Hayward WS (1997) Bic, a novel gene activated by proviral insertions in avian leukosis virus-induced lymphomas, is likely to function through its noncoding rna. Mol Cell Biol 17(3):1490–1502PubMed Tam W, Ben-Yehuda D, Hayward WS (1997) Bic, a novel gene activated by proviral insertions in avian leukosis virus-induced lymphomas, is likely to function through its noncoding rna. Mol Cell Biol 17(3):1490–1502PubMed
30.
go back to reference Tam W, Hughes SH, Hayward WS, Besmer P (2002) Avian bic, a gene isolated from a common retroviral site in avian leukosis virus-induced lymphomas that encodes a noncoding rna, cooperates with c-myc in lymphomagenesis and erythroleukemogenesis. J Virol 76(9):4275–4286CrossRefPubMed Tam W, Hughes SH, Hayward WS, Besmer P (2002) Avian bic, a gene isolated from a common retroviral site in avian leukosis virus-induced lymphomas that encodes a noncoding rna, cooperates with c-myc in lymphomagenesis and erythroleukemogenesis. J Virol 76(9):4275–4286CrossRefPubMed
31.
go back to reference Akiyama Y, Kato S, Iwa N (1973) Continuous cell culture from lymphoma of marek’s disease. Biken J 16(4):177–179PubMed Akiyama Y, Kato S, Iwa N (1973) Continuous cell culture from lymphoma of marek’s disease. Biken J 16(4):177–179PubMed
32.
go back to reference Hirai K, Yamada M, Arao Y, Kato S, Nii S (1990) Replicating marek’s disease virus (mdv) serotype 2 DNA with inserted mdv serotype 1 DNA sequences in a marek’s disease lymphoblastoid cell line msb1-41c. Arch Virol 114(3–4):153–165CrossRefPubMed Hirai K, Yamada M, Arao Y, Kato S, Nii S (1990) Replicating marek’s disease virus (mdv) serotype 2 DNA with inserted mdv serotype 1 DNA sequences in a marek’s disease lymphoblastoid cell line msb1-41c. Arch Virol 114(3–4):153–165CrossRefPubMed
33.
go back to reference Clop A, Marcq F, Takeda H, Pirottin D, Tordoir X, Bibe B, Bouix J, Caiment F, Elsen JM, Eychenne F, Larzul C, Laville E, Meish F, Milenkovic D, Tobin J, Charlier C, Georges M (2006) A mutation creating a potential illegitimate microrna target site in the myostatin gene affects muscularity in sheep. Nat Genet 38(7):813–818CrossRefPubMed Clop A, Marcq F, Takeda H, Pirottin D, Tordoir X, Bibe B, Bouix J, Caiment F, Elsen JM, Eychenne F, Larzul C, Laville E, Meish F, Milenkovic D, Tobin J, Charlier C, Georges M (2006) A mutation creating a potential illegitimate microrna target site in the myostatin gene affects muscularity in sheep. Nat Genet 38(7):813–818CrossRefPubMed
34.
go back to reference Fragnet L, Kut E, Rasschaert D (2005) Comparative functional study of the viral telomerase rna based on natural mutations. J Biol Chem 280(25):23502–23515CrossRefPubMed Fragnet L, Kut E, Rasschaert D (2005) Comparative functional study of the viral telomerase rna based on natural mutations. J Biol Chem 280(25):23502–23515CrossRefPubMed
35.
go back to reference Djeraba-AitLounis A, Soubieux D, Klapper W, Rasschaert D (2004) Induction of telomerase activity in avian lymphoblastoid cell line transformed by marek’s disease virus, mdcc-msb1. Vet Pathol 41(4):405–407CrossRefPubMed Djeraba-AitLounis A, Soubieux D, Klapper W, Rasschaert D (2004) Induction of telomerase activity in avian lymphoblastoid cell line transformed by marek’s disease virus, mdcc-msb1. Vet Pathol 41(4):405–407CrossRefPubMed
36.
go back to reference Lewis BP, Burge CB, Bartel DP (2005) Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microrna targets. Cell 120(1):15–20CrossRefPubMed Lewis BP, Burge CB, Bartel DP (2005) Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microrna targets. Cell 120(1):15–20CrossRefPubMed
37.
go back to reference Ceppi M, Pereira PM, Dunand-Sauthier I, Barras E, Reith W, Santos MA, Pierre P (2009) Microrna-155 modulates the interleukin-1 signaling pathway in activated human monocyte-derived dendritic cells. Proc Natl Acad Sci USA 106(8):2735–2740CrossRefPubMed Ceppi M, Pereira PM, Dunand-Sauthier I, Barras E, Reith W, Santos MA, Pierre P (2009) Microrna-155 modulates the interleukin-1 signaling pathway in activated human monocyte-derived dendritic cells. Proc Natl Acad Sci USA 106(8):2735–2740CrossRefPubMed
38.
go back to reference Tay Y, Zhang J, Thomson AM, Lim B, Rigoutsos I (2008) Micrornas to nanog, oct4 and sox2 coding regions modulate embryonic stem cell differentiation. Nature 455(7216):1124–1128CrossRefPubMed Tay Y, Zhang J, Thomson AM, Lim B, Rigoutsos I (2008) Micrornas to nanog, oct4 and sox2 coding regions modulate embryonic stem cell differentiation. Nature 455(7216):1124–1128CrossRefPubMed
39.
go back to reference Yeung ML, Yasunaga J, Bennasser Y, Dusetti N, Harris D, Ahmad N, Matsuoka M, Jeang KT (2008) Roles for micrornas, mir-93 and mir-130b, and tumor protein 53-induced nuclear protein 1 tumor suppressor in cell growth dysregulation by human t-cell lymphotrophic virus 1. Cancer Res 68(21):8976–8985CrossRefPubMed Yeung ML, Yasunaga J, Bennasser Y, Dusetti N, Harris D, Ahmad N, Matsuoka M, Jeang KT (2008) Roles for micrornas, mir-93 and mir-130b, and tumor protein 53-induced nuclear protein 1 tumor suppressor in cell growth dysregulation by human t-cell lymphotrophic virus 1. Cancer Res 68(21):8976–8985CrossRefPubMed
40.
go back to reference O’Hara AJ, Chugh P, Wang L, Netto EM, Luz E, Harrington WJ, Dezube BJ, Damania B, Dittmer DP (2009) Pre-micro rna signatures delineate stages of endothelial cell transformation in kaposi sarcoma. PLoS Pathog 5(4):e1000389CrossRefPubMed O’Hara AJ, Chugh P, Wang L, Netto EM, Luz E, Harrington WJ, Dezube BJ, Damania B, Dittmer DP (2009) Pre-micro rna signatures delineate stages of endothelial cell transformation in kaposi sarcoma. PLoS Pathog 5(4):e1000389CrossRefPubMed
41.
go back to reference Umbach JL, Cullen BR (2009) In-depth analysis of kaposi’s sarcoma-associated herpesvirus microrna expression provides insights into the mammalian microrna-processing machinery. J Virol 84(2):695–703CrossRefPubMed Umbach JL, Cullen BR (2009) In-depth analysis of kaposi’s sarcoma-associated herpesvirus microrna expression provides insights into the mammalian microrna-processing machinery. J Virol 84(2):695–703CrossRefPubMed
42.
go back to reference Godshalk SE, Bhaduri-McIntosh S, Slack FJ (2008) Epstein-barr virus-mediated dysregulation of human microrna expression. Cell Cycle 7(22):3595–3600PubMed Godshalk SE, Bhaduri-McIntosh S, Slack FJ (2008) Epstein-barr virus-mediated dysregulation of human microrna expression. Cell Cycle 7(22):3595–3600PubMed
43.
go back to reference Cameron JE, Fewell C, Yin Q, McBride J, Wang X, Lin Z, Flemington EK (2008) Epstein-barr virus growth/latency iii program alters cellular microrna expression. Virology 382(2):257–266CrossRefPubMed Cameron JE, Fewell C, Yin Q, McBride J, Wang X, Lin Z, Flemington EK (2008) Epstein-barr virus growth/latency iii program alters cellular microrna expression. Virology 382(2):257–266CrossRefPubMed
44.
go back to reference Wang FZ, Weber F, Croce C, Liu CG, Liao X, Pellett PE (2008) Human cytomegalovirus infection alters the expression of cellular microrna species that affect its replication. J Virol 82(18):9065–9074CrossRefPubMed Wang FZ, Weber F, Croce C, Liu CG, Liao X, Pellett PE (2008) Human cytomegalovirus infection alters the expression of cellular microrna species that affect its replication. J Virol 82(18):9065–9074CrossRefPubMed
45.
go back to reference Okamura K, Phillips MD, Tyler DM, Duan H, Chou YT, Lai EC (2008) The regulatory activity of microrna* species has substantial influence on microrna and 3’ utr evolution. Nat Struct Mol Biol 15(4):354–363CrossRefPubMed Okamura K, Phillips MD, Tyler DM, Duan H, Chou YT, Lai EC (2008) The regulatory activity of microrna* species has substantial influence on microrna and 3’ utr evolution. Nat Struct Mol Biol 15(4):354–363CrossRefPubMed
46.
go back to reference Okamura K, Liu N, Lai EC (2009) Distinct mechanisms for microrna strand selection by drosophila argonautes. Mol Cell 36(3):431–444CrossRefPubMed Okamura K, Liu N, Lai EC (2009) Distinct mechanisms for microrna strand selection by drosophila argonautes. Mol Cell 36(3):431–444CrossRefPubMed
47.
48.
go back to reference Lin EA, Kong L, Bai XH, Luan Y, Liu CJ (2009) Mir-199a, a bone morphogenic protein 2-responsive microrna, regulates chondrogenesis via direct targeting to smad1. J Biol Chem 284(17):11326–11335CrossRefPubMed Lin EA, Kong L, Bai XH, Luan Y, Liu CJ (2009) Mir-199a, a bone morphogenic protein 2-responsive microrna, regulates chondrogenesis via direct targeting to smad1. J Biol Chem 284(17):11326–11335CrossRefPubMed
49.
go back to reference Ro S, Park C, Young D, Sanders KM, Yan W (2007) Tissue-dependent paired expression of mirnas. Nucleic Acids Res 35(17):5944–5953CrossRefPubMed Ro S, Park C, Young D, Sanders KM, Yan W (2007) Tissue-dependent paired expression of mirnas. Nucleic Acids Res 35(17):5944–5953CrossRefPubMed
50.
51.
52.
go back to reference Umbach JL, Kramer MF, Jurak I, Karnowski HW, Coen DM, Cullen BR (2008) Micrornas expressed by herpes simplex virus 1 during latent infection regulate viral mrnas. Nature 454(7205):780–783PubMed Umbach JL, Kramer MF, Jurak I, Karnowski HW, Coen DM, Cullen BR (2008) Micrornas expressed by herpes simplex virus 1 during latent infection regulate viral mrnas. Nature 454(7205):780–783PubMed
55.
go back to reference Vigorito E, Perks KL, Abreu-Goodger C, Bunting S, Xiang Z, Kohlhaas S, Das PP, Miska EA, Rodriguez A, Bradley A, Smith KG, Rada C, Enright AJ, Toellner KM, Maclennan IC, Turner M (2007) Microrna-155 regulates the generation of immunoglobulin class-switched plasma cells. Immunity 27(6):847–859CrossRefPubMed Vigorito E, Perks KL, Abreu-Goodger C, Bunting S, Xiang Z, Kohlhaas S, Das PP, Miska EA, Rodriguez A, Bradley A, Smith KG, Rada C, Enright AJ, Toellner KM, Maclennan IC, Turner M (2007) Microrna-155 regulates the generation of immunoglobulin class-switched plasma cells. Immunity 27(6):847–859CrossRefPubMed
56.
go back to reference Djeraba A, Bernardet N, Dambrine G, Quere P (2000) Nitric oxide inhibits marek’s disease virus replication but is not the single decisive factor in interferon-gamma-mediated viral inhibition. Virology 277(1):58–65CrossRefPubMed Djeraba A, Bernardet N, Dambrine G, Quere P (2000) Nitric oxide inhibits marek’s disease virus replication but is not the single decisive factor in interferon-gamma-mediated viral inhibition. Virology 277(1):58–65CrossRefPubMed
57.
go back to reference He M, Xu Z, Ding T, Kuang DM, Zheng L (2009) Microrna-155 regulates inflammatory cytokine production in tumor-associated macrophages via targeting c/ebpbeta. Cell Mol Immunol 6(5):343–352CrossRefPubMed He M, Xu Z, Ding T, Kuang DM, Zheng L (2009) Microrna-155 regulates inflammatory cytokine production in tumor-associated macrophages via targeting c/ebpbeta. Cell Mol Immunol 6(5):343–352CrossRefPubMed
58.
go back to reference Wang X, Zhao Q, Matta R, Meng X, Liu X, Liu CG, Nelin LD, Liu Y (2009) Inducible nitric-oxide synthase expression is regulated by mitogen-activated protein kinase phosphatase-1. J Biol Chem 284(40):27123–27134CrossRefPubMed Wang X, Zhao Q, Matta R, Meng X, Liu X, Liu CG, Nelin LD, Liu Y (2009) Inducible nitric-oxide synthase expression is regulated by mitogen-activated protein kinase phosphatase-1. J Biol Chem 284(40):27123–27134CrossRefPubMed
59.
go back to reference Schat KA, Nair V (2008) Marek’s disease. In: SY M (ed) Disease of poultry, chapter 15, Neoplastic Diseases, pp 452–514 Schat KA, Nair V (2008) Marek’s disease. In: SY M (ed) Disease of poultry, chapter 15, Neoplastic Diseases, pp 452–514
60.
go back to reference Murphy E, Vanicek J, Robins H, Shenk T, Levine AJ (2008) Suppression of immediate-early viral gene expression by herpesvirus-coded micrornas: implications for latency. Proc Natl Acad Sci USA 105(14):5453–5458CrossRefPubMed Murphy E, Vanicek J, Robins H, Shenk T, Levine AJ (2008) Suppression of immediate-early viral gene expression by herpesvirus-coded micrornas: implications for latency. Proc Natl Acad Sci USA 105(14):5453–5458CrossRefPubMed
Metadata
Title
Marek’s disease virus microRNA designated Mdv1-pre-miR-M4 targets both cellular and viral genes
Authors
Benoît Muylkens
Damien Coupeau
Ginette Dambrine
Sascha Trapp
Denis Rasschaert
Publication date
01-11-2010
Publisher
Springer Vienna
Published in
Archives of Virology / Issue 11/2010
Print ISSN: 0304-8608
Electronic ISSN: 1432-8798
DOI
https://doi.org/10.1007/s00705-010-0777-y

Other articles of this Issue 11/2010

Archives of Virology 11/2010 Go to the issue