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The Rrp6 C-terminal domain binds RNA and activates the nuclear RNA exosome.
Wasmuth, Elizabeth V; Lima, Christopher D.
Afiliação
  • Wasmuth EV; Structural Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.
  • Lima CD; Structural Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA limac@mskcc.org.
Nucleic Acids Res ; 45(2): 846-860, 2017 01 25.
Article em En | MEDLINE | ID: mdl-27899565
The eukaryotic RNA exosome is an essential, multi-subunit complex that catalyzes RNA turnover, maturation, and quality control processes. Its non-catalytic donut-shaped core includes 9 subunits that associate with the 3' to 5' exoribonucleases Rrp6, and Rrp44/Dis3, a subunit that also catalyzes endoribonuclease activity. Although recent structures and biochemical studies of RNA bound exosomes from S. cerevisiae revealed that the Exo9 central channel guides RNA to either Rrp6 or Rrp44 using partially overlapping and mutually exclusive paths, several issues related to RNA recruitment remain. Here, we identify activities for the highly basic Rrp6 C-terminal tail that we term the 'lasso' because it binds RNA and stimulates ribonuclease activities associated with Rrp44 and Rrp6 within the 11-subunit nuclear exosome. Stimulation is dependent on the Exo9 central channel, and the lasso contributes to degradation and processing activities of exosome substrates in vitro and in vivo. Finally, we present evidence that the Rrp6 lasso may be a conserved feature of the eukaryotic RNA exosome.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: RNA / Exorribonucleases / Domínios e Motivos de Interação entre Proteínas / Complexo Multienzimático de Ribonucleases do Exossomo Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: RNA / Exorribonucleases / Domínios e Motivos de Interação entre Proteínas / Complexo Multienzimático de Ribonucleases do Exossomo Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article