2B.V demarcates divergent strand-switch regions, some tDNA loci, and genome compartments in Trypanosoma cruzi and affects parasite differentiation and host cell invasio

Autor(es):Mostrar menos -

Roson, Juliana Nunes ^{[1, 2, 3]} ; Vitarelli, Marcela de Oliveira J. ^{[2, 3]} ; Costa-Silva, Hellida Marina ^{[2, 3]} ; Pereira, Kamille Schmitt ^{[4, 5]} ; Pires, David da Silva ^{[2, 3]} ; Lopes, Leticia de Sousa ^{[2, 3]} ; Cordeiro, Barbara ^{[2, 3]} ; Kraus, Amelie ^{[6, 7]} ; Cruz, Karin Navarro Tozzi ^{[2, 3]} ; Calderano, Simone Guedes ^{[2, 3]} ; Fragoso, Stenio Perdigao ^{[4, 5]} ; Siegel, T. Nicolai ^{[6, 7]} ; Elias, Maria Carolina ^{[2, 3]} ; da Cunha, Julia Pinheiro Chagas ^{[2, 3]}

Afiliação do(s) autor(es)

^[1] Escola Paulista Med UNIFESP, Dept Microbiol Immunol & Parasitol, Sao Paulo - Brazil

^[2] Butantan Inst, Lab Cell Cycle, Sao Paulo - Brazil

^[3] Butantan Inst, Ctr Toxins Immune Response & Cell Signaling CeTIC, Sao Paulo - Brazil

^[4] Univ Fed Parana, Dept Bioproc & Biotechnol, Curitiba, Parana - Brazil

^[5] Fiocruz MS, Carlos Chagas Inst, Lab Mol & Syst Biol Trypanosomatids, Curitiba, Parana - Brazil

^[6] Ludwig Maximilians Univ Munchen, Div Expt Parasitol, Fac Vet Med, Munich - Germany

^[7] Ludwig Maximilians Univ Munch, Div Physiol Chem, Biomed Ctr, Fac Med, Munich - Germany

• Tipo de documento: Artigo Científico
• Fonte: PLOS PATHOGENS; v. 18, n. 2 FEB 2022.
• Citações Web of Science: 0

Resumo

Author summaryTrypanosomatids have to adapt to different environmental conditions, changing their morphology, gene expression and metabolism. These organisms have many unique features in terms of gene expression regulation. The genomic organization includes polycistronic regions with the absence of well-defined transcription start sites. In T. brucei, histone variants mark the start and ending sites of transcription; however, little is known about whether these proteins change their genome location, expression levels and interactors along life forms and what the impact is of these changes on parasite differentiation and infection. In T. cruzi, the causative agent of Chagas disease, we previously found that the histone variant of H2B is enriched in TCT forms, a nonreplicative and infective form, suggesting that this variant may contribute to the differences in chromatin structure and global transcription rates observed among these life forms. Here, we aimed to go one step further and performed the first histone ChIP-seq analysis in T. cruzi, in which we found that H2B.V was enriched at divergent strand switch regions, some tDNA loci and other critical genomic regions associated with T. cruzi genome compartments. We found that H2B.V interacts with a bromodomain factor, suggesting an intricate network involving chromatin acetylation around H2B.V enriched sites. Moreover, parasites expressing reduced H2B.V levels were associated with higher rates of differentiation and mammalian cell infectivity. Histone variants play a crucial role in chromatin structure organization and gene expression. Trypanosomatids have an unusual H2B variant (H2B.V) that is known to dimerize with the variant H2A.Z generating unstable nucleosomes. Previously, we found that H2B.V protein is enriched in tissue-derived trypomastigote (TCT) life forms, a nonreplicative stage of Trypanosoma cruzi, suggesting that this variant may contribute to the differences in chromatin structure and global transcription rates observed among parasite life forms. Here, we performed the first genome-wide profiling of histone localization in T. cruzi using epimastigotes and TCT life forms, and we found that H2B.V was preferentially located at the edges of divergent transcriptional strand switch regions, which encompass putative transcriptional start regions; at some tDNA loci; and between the conserved and disrupted genome compartments, mainly at trans-sialidase, mucin and MASP genes. Remarkably, the chromatin of TCT forms was depleted of H2B.V-enriched peaks in comparison to epimastigote forms. Interactome assays indicated that H2B.V associated specifically with H2A.Z, bromodomain factor 2, nucleolar proteins and a histone chaperone, among others. Parasites expressing reduced H2B.V levels were associated with higher rates of parasite differentiation and mammalian cell infectivity. Taken together, H2B.V demarcates critical genomic regions and associates with regulatory chromatin proteins, suggesting a scenario wherein local chromatin structures associated with parasite differentiation and invasion are regulated during the parasite life cycle. (AU)

• Processo FAPESP: 18/15553-9 - Indo a fundo na regulação da cromatina de Trypanosoma cruzi: identificação de novas moléculas e questionando seu possível impacto no controle da transcrição
• Beneficiário: Julia Pinheiro Chagas da Cunha
• Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores - Fase 2
• Processo FAPESP: 16/50050-2 - How do common and diverged features of the replicative stress response shape the biology of TriTryp parasites?
• Beneficiário: Maria Carolina Quartim Barbosa Elias Sabbaga
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 17/06104-3 - Análise funcional da histona H2B variante de Trypanosoma cruzi
• Beneficiário: Julia Pinheiro Chagas da Cunha
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 19/04483-2 - Dinâmica funcional da proteína Orc1b: análise por ChIP-seq
• Beneficiário: Marcela de Oliveira Vitarelli
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Doutorado
• Processo FAPESP: 19/16033-1 - Estudo nos sítios de início e final de transcrição da RNA polimerase II de Trypanosoma cruzi
• Beneficiário: Juliana Nunes Rosón
• Modalidade de apoio: Bolsas no Brasil - Doutorado
• Processo FAPESP: 13/07467-1 - CeTICS - Centro de Toxinas, Imuno-Resposta e Sinalização Celular
• Beneficiário: Hugo Aguirre Armelin
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
• Processo FAPESP: 19/19834-5 - Descrevendo novas moléculas na cromatina de Trypanosoma cruzi por imunoprecipitação de cromatina locus específica
• Beneficiário: Hellida Marina Costa Silva
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado