The Rb binding domain of HPV31 E7 is required to maintain high levels of DNA repair factors in infected cells

Bryan Johnson, Heather L. Aloor, Cary A. Moody

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Human papillomaviruses (HPV) exhibit constitutive activation of ATM and ATR DNA damage response (DDR) pathways, which are required for productive viral replication. Expression of HPV31 E7 alone is sufficient to activate the DDR through an unknown mechanism. Here, we demonstrate that the E7 Rb binding domain is required to increase levels of many DDR proteins, including ATM, Chk2, Chk1, the MRN components MRE11, Rad50, and NBS1, as well as the homologous recombination repair proteins BRCA1 and Rad51. Interestingly, we have found that the increase in these DNA repair proteins does not occur solely at the level of transcription, but that E7 broadly increases the half-life of these DDR factors, a phenotype that is lost in the E7 Rb binding mutant. These data suggest that HPV-31 upregulates DNA repair factors necessary for replication by increasing protein half-life in a manner requiring the E7 Rb binding domain.

Original languageEnglish (US)
Pages (from-to)22-34
Number of pages13
JournalVirology
Volume500
DOIs
StatePublished - Jan 1 2017
Externally publishedYes

Fingerprint

DNA Repair
DNA Damage
Half-Life
Human papillomavirus 31
Ataxia Telangiectasia Mutated Proteins
BRCA1 Protein
Recombinational DNA Repair
Proteins
Up-Regulation
Phenotype

Keywords

  • DNA damage response
  • Human papillomavirus
  • Replication
  • Virus

ASJC Scopus subject areas

  • Virology

Cite this

The Rb binding domain of HPV31 E7 is required to maintain high levels of DNA repair factors in infected cells. / Johnson, Bryan; Aloor, Heather L.; Moody, Cary A.

In: Virology, Vol. 500, 01.01.2017, p. 22-34.

Research output: Contribution to journalArticle

Johnson, Bryan ; Aloor, Heather L. ; Moody, Cary A. / The Rb binding domain of HPV31 E7 is required to maintain high levels of DNA repair factors in infected cells. In: Virology. 2017 ; Vol. 500. pp. 22-34.
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