Replication origin location might contribute to genetic variability in Trypanosoma cruzi

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dc.contributor(LCC) Lab. Ciclo Celularpt_BR
dc.contributor(CeTICS) Centro de Toxinas, Resposta-imune e Sinalização Celularpt_BR
dc.contributor(LETA) Lab. Toxinologia Aplicadapt_BR
dc.contributor.authorde Araujo, Christiane Bezerrapt_BR
dc.contributor.authorda Cunha, Julia Pinheiro Chagaspt_BR
dc.contributor.authorInada, Davi Toshiopt_BR
dc.contributor.authorDamasceno, Jezielpt_BR
dc.contributor.authorLima, Alex Ranieri Jerônimopt_BR
dc.contributor.authorHiraiwa, Priscilapt_BR
dc.contributor.authorMarques, Catarinapt_BR
dc.contributor.authorGonçalves, Evonnildopt_BR
dc.contributor.authorNishiyama Junior, Milton Yutakapt_BR
dc.contributor.authorMcCulloch, Richard D.pt_BR
dc.contributor.authorElias, Maria Carolinapt_BR
dc.date.accessioned2020-07-09T21:28:14Z-
dc.date.available2020-07-09T21:28:14Z-
dc.date.issued2020pt_BR
dc.identifier.citationde Araujo CB, da Cunha JPC, Inada DT, Damasceno J, Lima ARJ, Hiraiwa P, et al. Replication origin location might contribute to genetic variability in Trypanosoma cruzi. BMC Genomics. 2020 Jun;21:414. doi:10.1186/s12864-020-06803-8.pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/3076-
dc.description.abstractBackground DNA replication in trypanosomatids operates in a uniquely challenging environment, since most of their genomes are constitutively transcribed. Trypanosoma cruzi, the etiological agent of Chagas disease, presents high variability in both chromosomes size and copy number among strains, though the underlying mechanisms are unknown. Results Here we have mapped sites of DNA replication initiation across the T. cruzi genome using Marker Frequency Analysis, which has previously only been deployed in two related trypanosomatids. The putative origins identified in T. cruzi show a notable enrichment of GC content, a preferential position at subtelomeric regions, coinciding with genes transcribed towards the telomeres, and a pronounced enrichment within coding DNA sequences, most notably in genes from the Dispersed Gene Family 1 (DGF-1). Conclusions These findings suggest a scenario where collisions between DNA replication and transcription are frequent, leading to increased genetic variability, as seen by the increase SNP levels at chromosome subtelomeres and in DGF-1 genes containing putative origins.pt_BR
dc.description.sponsorship(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulopt_BR
dc.description.sponsorship(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológicopt_BR
dc.description.sponsorship(BBSRC) Biotechnology and Biological Sciences Research Councilpt_BR
dc.description.sponsorshipWellcome Trustpt_BR
dc.description.sponsorship(FCT) Fundação para a Ciência e a Tecnologiapt_BR
dc.description.sponsorship(EC) European Commissionpt_BR
dc.format.extent414pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofBMC Genomicspt_BR
dc.rightsOpen accesspt_BR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_BR
dc.titleReplication origin location might contribute to genetic variability in Trypanosoma cruzipt_BR
dc.typeArticlept_BR
dc.rights.licenseCC BYpt_BR
dc.identifier.doi10.1186/s12864-020-06803-8pt_BR
dc.identifier.urlhttps://doi.org/10.1186/s12864-020-06803-8pt_BR
dc.contributor.externalUniversity of Glasgowpt_BR
dc.contributor.external(UFPA) Universidade Federal do Parápt_BR
dc.contributor.external(ICC-FIOCRUZ) Instituto Carlos Chagaspt_BR
dc.identifier.citationvolume21pt_BR
dc.subject.keywordreplication originspt_BR
dc.subject.keywordTrypanosoma cruzipt_BR
dc.subject.keywordgenetic variabilitypt_BR
dc.subject.keywordDGF-1pt_BR
dc.relation.ispartofabbreviatedBMC Genomicspt_BR
dc.identifier.citationabntv. 21, 414, jun. 2020pt_BR
dc.identifier.citationvancouver2020 Jun;21:414pt_BR
dc.contributor.butantanDe Araujo, Christiane Bezerra|:Aluno|:LCC - Laboratório de Ciclo Celular|:PrimeiroAutorpt_BR
dc.contributor.butantanda Cunha, Julia Pinheiro Chagas|:Pesquisador|:LCC - Laboratório de Ciclo Celular:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS)|:Autor de correspondênciapt_BR
dc.contributor.butantanInada, Davi Toshio|:Aluno|:LCC - Laboratório de Ciclo Celular:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS)|:pt_BR
dc.contributor.butantanNishiyama Junior, Milton Yutaka|:Pesquisador|:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS):(LETA) Lab. Toxinologia Aplicada|:pt_BR
dc.contributor.butantanElias, Maria Carolina|:Pesquisador|:LCC - Laboratório de Ciclo Celular:Centro de Toxinas, Resposta-imune e Sinalização Celular (CeTICS)|:Autor de correspondênciapt_BR
dc.contributor.butantanLima, Alex Ranieri Jerônimo|:LCC - Laboratório de Ciclo Celularpt_BR
dc.sponsorship.butantanBiotechnology and Biological Sciences Research Council (BBSRC)¦¦BB/N016165/1pt_BR
dc.sponsorship.butantanConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)¦¦304329/2015–0pt_BR
dc.sponsorship.butantanEuropean Commission (EC)¦¦750259pt_BR
dc.sponsorship.butantanFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)¦¦2013/07467–1pt_BR
dc.sponsorship.butantanFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)¦¦2016/50050–2pt_BR
dc.sponsorship.butantanFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)¦¦2014/24170–5pt_BR
dc.sponsorship.butantanFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)¦¦2014/13375–5pt_BR
dc.sponsorship.butantanFundação para a Ciência e a Tecnologia (FCT)¦¦SFRH/BD/68784/2010pt_BR
dc.sponsorship.butantanWellcome Trust¦¦083485pt_BR
dc.sponsorship.butantanWellcome Trust¦¦104111pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
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