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Trypanosoma brucei RRP44 is involved in an early stage of large ribosomal subunit RNA maturation.
Cesaro, Giovanna; Carneiro, Flávia Raquel Gonçalves; Ávila, Andréa Rodrigues; Zanchin, Nilson Ivo Tonin; Guimarães, Beatriz Gomes.
Afiliação
  • Cesaro G; a Carlos Chagas Institute , Oswaldo Cruz Foundation, FIOCRUZ-PR , Curitiba , Brazil.
  • Carneiro FRG; b Biochemsitry Postgraduate Program , Federal University of Parana , Curitiba , Brazil.
  • Ávila AR; a Carlos Chagas Institute , Oswaldo Cruz Foundation, FIOCRUZ-PR , Curitiba , Brazil.
  • Zanchin NIT; c Center for Technology Development in Healthcare , Oswaldo Cruz Foundation , Rio de Janeiro , Brazil.
  • Guimarães BG; a Carlos Chagas Institute , Oswaldo Cruz Foundation, FIOCRUZ-PR , Curitiba , Brazil.
RNA Biol ; 16(1): 133-143, 2019 01.
Article em En | MEDLINE | ID: mdl-30593255
ABSTRACT
Ribosomal RNA precursors undergo a series of structural and chemical modifications to generate matured RNA molecules that will comprise ribosomes. This maturation process involves a large set of accessory proteins as well as ribonucleases, responsible for removal of the external and internal transcribed spacers from the pre-rRNA. Early-diverging eukaryotes belonging to the Kinetoplastida class display several unique characteristics, in particular in terms of RNA synthesis and maturation. These peculiarities include the rRNA biogenesis and the extensive fragmentation of the large ribosomal subunit (LSU) rRNA. The role of specific endo- and exonucleases in the maturation of the unusual rRNA precursor of trypanosomatids remains largely unknown. One of the nucleases involved in rRNA processing is Rrp44, an exosome associated ribonuclease in yeast, which is involved in several metabolic RNA pathways. Here, we investigated the function of Trypanosoma brucei RRP44 orthologue (TbRRP44) in rRNA processing. Our results revealed that TbRRP44 depletion causes unusual polysome profile and accumulation of the complete LSU rRNA precursor, in addition to 5.8S maturation impairment. We also determined the crystal structure of TbRRP44 endonucleolytic domain. Structural comparison with Saccharomyces cerevisiae Rrp44 revealed differences in the catalytic site and substitutions of surface residues, which could provide molecular bases for the lack of interaction of RRP44 with the exosome complex in T. brucei.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma brucei brucei / RNA Ribossômico / Proteínas de Protozoários / Processamento Pós-Transcricional do RNA / Complexo Multienzimático de Ribonucleases do Exossomo / Interações Hospedeiro-Parasita Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: RNA Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma brucei brucei / RNA Ribossômico / Proteínas de Protozoários / Processamento Pós-Transcricional do RNA / Complexo Multienzimático de Ribonucleases do Exossomo / Interações Hospedeiro-Parasita Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: RNA Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil