The human adenovirus type 5 E1B 55kDa protein interacts with RNA promoting timely DNA replication and viral late mRNA metabolism

PLoS One. 2019 Apr 3;14(4):e0214882. doi: 10.1371/journal.pone.0214882. eCollection 2019.

Abstract

The E1B 55kDa produced by human adenovirus type 5 is a multifunctional protein that participates in the regulation of several steps during the viral replication cycle. Previous studies suggest this protein plays an important role in postranscriptional regulation of viral and cellular gene expression, as it is required for the selective accumulation of maximal levels of viral late mRNA in the cytoplasm of the infected cell; however the molecular mechanisms that are altered or regulated by this protein have not been elucidated. A ribonucleoprotein motif that could implicate the direct interaction of the protein with RNA was initially predicted and tested in vitro, but the interaction with RNA could not be detected in infected cells, suggesting the interaction may be weak or transient. Here it was determined that the E1B 55kDa interacts with RNA in the context of the viral infection in non-transformed human cells, and its contribution to the adenovirus replication cycle was evaluated. Using recombinant adenoviruses with amino acid substitutions or a deletion in the ribonucleoprotein motif the interaction of E1B 55kDa with RNA was found to correlate with timely and efficient viral DNA replication and viral late mRNA accumulation and splicing.

MeSH terms

  • Adenovirus E1B Proteins / genetics
  • Adenovirus E1B Proteins / metabolism*
  • Adenoviruses, Human / genetics
  • Adenoviruses, Human / physiology*
  • Cell Line
  • Humans
  • RNA, Viral / genetics
  • RNA, Viral / metabolism*
  • Virus Replication / genetics
  • Virus Replication / physiology*

Substances

  • Adenovirus E1B Proteins
  • RNA, Viral

Grants and funding

BT received support from Consejo Nacional de Ciencia y Tecnología (CONACyT) Scholarship 266820, México. https://www.conacyt.gob.mx; PH received support from Consejo Nacional de Ciencia y Tecnología (CONACyT) Scholarship 447442, México. https://www.conacyt.gob.mx; RAG was supported by grants from CONACyT CB-2011-01-168497 and Programa para el Desarrollo Profesional Docente-Secretaría de Educación Pública (PRODEP-SEP). http://www.dgesu.ses.sep.gob.mx/prodep.htm; TD and the Heinrich Pette Institute is supported by the Freie und Hansestadt Hamburg and the Bundesministerium für Gesundheit (BMG). https://www.bundesgesundheitsministerium.de/; R.A.G. and T.D. received support from the Research Group Linkage Program of the Alexander von Humboldt Foundation. https://www.humboldt-foundation.de/web/home.html; NO - The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.