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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Human RNF113A participates of pre-mRNA splicing in vitro

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Autor(es):
Gatti da Silva, Guilherme H. [1] ; Jurica, Melissa S. [2] ; Chagas da Cunha, Julia P. [3] ; Oliveira, Carla C. [4] ; Coltri, Patricia P. [4, 2, 1]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Cell & Dev Biol, Av Prof Lineu Prestes 1524, S425-ICB-1, BR-05508000 Sao Paulo - Brazil
[2] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 - USA
[3] Butantan Inst, Special Lab Cell Cycle, Sao Paulo - Brazil
[4] Univ Sao Paulo, Inst Chem, Dept Biochem, Sao Paulo - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: Journal of Cellular Biochemistry; v. 120, n. 5, p. 8764-8774, MAY 2019.
Citações Web of Science: 1
Resumo

Pre-messenger RNA (mRNA) splicing is an essential step in the control of eukaryotic gene expression. During splicing, the introns are removed from the gene transcripts as the exons are ligated to create mature mRNA sequences. Splicing is performed by the spliceosome, which is a macromolecular complex composed of five small nuclear RNAs (snRNAs) and more than 100 proteins. Except for the core snRNP proteins, most spliceosome proteins are transiently associated and presumably involved with the regulation of spliceosome activity. In this study, we explored the association and participation of the human protein RNF113A in splicing. The addition of excess recombinant RNF113A to in vitro splicing reactions results in splicing inhibition. In whole-cell lysates, RNF113A co-immunoprecipitated with U2, U4, and U6 snRNAs, which are components of the tri-snRNP, and with proteins PRP19 and BRR2. When HeLa cells were CRISPR-edited to reduce the RNF113A levels, the in vitro splicing efficiency was severely affected. Consistently, the splicing activity was partially restored after the addition of the recombinant GST-RNF113A. On the basis on these results, we propose a model in which RNF113A associates with the spliceosome by interacting with PRP19, promoting essential rearrangements that lead to splicing. (AU)

Processo FAPESP: 10/51842-3 - SMOLBNET2: estudo de estrutura de proteínas componentes e reguladoras do exossomo de Archaea e de levedura
Beneficiário:Carla Columbano de Oliveira
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 13/02738-7 - Caracterização do papel de proteínas reguladoras do splicing em eucariotos
Beneficiário:Patricia Pereira Coltri
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 11/20664-5 - Caracterização funcional da proteína ZNF183 no spliceossomo em mamíferos
Beneficiário:Patricia Pereira Coltri
Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Pós-Doutorado
Processo FAPESP: 17/06994-9 - Regulação do splicing de microRNAs em eucariotos
Beneficiário:Patricia Pereira Coltri
Modalidade de apoio: Auxílio à Pesquisa - Regular