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Pregled bibliografske jedinice broj: 715185

Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia


Kramer, M.F.; Jurak, Igor; Pesola, J.M.; Boissel, S.; Knipe, D.M.; Coen, D.M.
Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia // Virology, 417 (2011), 2; 239-247 doi:10.1016/j.virol.2011.06.027 (podatak o recenziji nije dostupan, prethodno priopćenje, znanstveni)


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Naslov
Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia

Autori
Kramer, M.F. ; Jurak, Igor ; Pesola, J.M. ; Boissel, S. ; Knipe, D.M. ; Coen, D.M.

Izvornik
Virology (0042-6822) 417 (2011), 2; 239-247

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, prethodno priopćenje, znanstveni

Ključne riječi
miRNA latency; Herpes simplex virus; microRNAs; latency; gene regulation

Sažetak
Several herpes simplex virus 1 microRNAs are encoded within or near the latency associated transcript (LAT) locus, and are expressed abundantly during latency. Some of these microRNAs can repress the expression of important viral proteins and are hypothesized to play important roles in establishing and/or maintaining latent infections. We found that in lytically infected cells and in acutely infected mouse ganglia, expression of LAT-encoded microRNAs was weak and unaffected by a deletion that includes the LAT promoter. In mouse ganglia latently infected with wild type virus, the microRNAs accumulated to high levels, but deletions of the LAT promoter markedly reduced expression of LAT-encoded microRNAs and also miR-H6, which is encoded upstream of LAT and can repress expression of ICP4. Because these LAT deletion mutants establish and maintain latent infections, these microRNAs are not essential for latency, at least in mouse trigeminal ganglia, but may help promote it.

Izvorni jezik
Engleski



POVEZANOST RADA


Profili:

Avatar Url Igor Jurak (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com

Citiraj ovu publikaciju:

Kramer, M.F.; Jurak, Igor; Pesola, J.M.; Boissel, S.; Knipe, D.M.; Coen, D.M.
Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia // Virology, 417 (2011), 2; 239-247 doi:10.1016/j.virol.2011.06.027 (podatak o recenziji nije dostupan, prethodno priopćenje, znanstveni)
Kramer, M., Jurak, I., Pesola, J., Boissel, S., Knipe, D. & Coen, D. (2011) Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia. Virology, 417 (2), 239-247 doi:10.1016/j.virol.2011.06.027.
@article{article, author = {Kramer, M.F. and Jurak, Igor and Pesola, J.M. and Boissel, S. and Knipe, D.M. and Coen, D.M.}, year = {2011}, pages = {239-247}, DOI = {10.1016/j.virol.2011.06.027}, keywords = {miRNA latency, Herpes simplex virus, microRNAs, latency, gene regulation}, journal = {Virology}, doi = {10.1016/j.virol.2011.06.027}, volume = {417}, number = {2}, issn = {0042-6822}, title = {Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia}, keyword = {miRNA latency, Herpes simplex virus, microRNAs, latency, gene regulation} }
@article{article, author = {Kramer, M.F. and Jurak, Igor and Pesola, J.M. and Boissel, S. and Knipe, D.M. and Coen, D.M.}, year = {2011}, pages = {239-247}, DOI = {10.1016/j.virol.2011.06.027}, keywords = {miRNA latency, Herpes simplex virus, microRNAs, latency, gene regulation}, journal = {Virology}, doi = {10.1016/j.virol.2011.06.027}, volume = {417}, number = {2}, issn = {0042-6822}, title = {Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia}, keyword = {miRNA latency, Herpes simplex virus, microRNAs, latency, gene regulation} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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