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Characterization of molecular attributes that influence LINE-1 restriction by all seven human APOBEC3 proteins.
Renner, Tyler Milston; Bélanger, Kasandra; Goodwin, Laura Rose; Campbell, Mark; Langlois, Marc-André.
Afiliação
  • Renner TM; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Bélanger K; Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.
  • Goodwin LR; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Campbell M; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Langlois MA; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada. Electronic address: langlois@uottawa.ca.
Virology ; 520: 127-136, 2018 07.
Article em En | MEDLINE | ID: mdl-29860216
LINE-1 (L1) is a non-long terminal repeat (LTR) retrotransposon inserted throughout the human genome. APOBEC3 (A3) proteins are part of a network of host intrinsic defenses capable of restricting retroviruses and the replication of L1 retroelements. These enzymes inactivate retroviruses primarily through deamination of single-stranded viral DNA. In contrast, only A3A deaminates L1 DNA, while the other six A3 proteins restrict L1 to varying degrees through yet poorly defined mechanisms. Here we provide further insight into the molecular attributes of L1 restriction by A3 proteins. We specifically investigated the roles of A3 protein oligomerization, interactions with RNA and their binding to the various L1 proteins. Our results show that compromising the ability of A3 proteins to oligomerize or interact with a nucleic acid substrate diminished L1 restriction to varying degrees. However the efficiency of their binding to L1 proteins did not predict restriction or the potency of the restriction.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos Nucleotídeos Longos e Dispersos / Citosina Desaminase Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Virology Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Elementos Nucleotídeos Longos e Dispersos / Citosina Desaminase Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Virology Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá