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| Registros recuperados : 21 | |
| 3. |  | AOYAGI, L. N.; CAITAR, V. S. L.; POLIZEL-PODANOSQUI, A. M.; DARBEN, L. M.; CARVALHO, M. C. D.; KUWAHARA, M. K.; MARCELINO-GUIMARÃES, F. C. Identificação e caracterização filogenética de proteínas R2R3-MYB no genoma da soja e seu perfil transcricional em resposta a patógenos. In: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 46.; REUNIÃO BRASILEIRA DE CONTROLE BIOLÓGICO, 11., 2013, Ouro Preto. [Anais...]. [Brasília]: Sociedade Brasileira de Fitopatologia, 2013. 1 CD-ROM.| Biblioteca(s): Embrapa Soja. |
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| 4. | | DARBEN, L. M.; QI, M.; YOKOYAMA, A.; CARVALHO, M. C. C. G. de; ABDELNOOR, R. V.; WHITHAM, S. A.; MARCELINO-GUIMARÃES, F. C. Functional characterization of P. pachyrhizi effector candidates. In: INTERNATIONAL CONGRESS OF PLANT MOLECULAR BIOLOGY, 11., 2015, Iguassu Falls. Abstract... Abstract: 840.pdf.| Biblioteca(s): Embrapa Soja. |
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| 5. | | UTIYAMA, A. S.; ABE, V. Y.; DARBEN, L. M.; CARVALHO, K.; CARVALHO, M. C. C. G. de; MARCELINO-GUIMARÃES, F. C. Avaliação funcional de proteínas candidatas a efetores de Phakopsora pachyrhizi por meio da análise de espécies reativas a oxigênio (ROS) e deposição de calose. In: JORNADA ACADÊMICA DA EMBRAPA SOJA, 13., 2018, Londrina. Resumos expandidos... Londrina: Embrapa Soja, 2018. p. 38-45.| Biblioteca(s): Embrapa Soja. |
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| 6. | | CAITAR, V. S. L.; NASCIMENTO, L. C.; CARVALHO, M. C. D. C. G. D.; DARBEN, L. M; PODANOSQUI, A. M. P.; DIAS, W. P.; GUIMARÃES, F. C. M. Earlier transcriptome interaction from resistant and susceptible soybean genotypes under Pratylenchus brachyurus infection revealed by RNA-seq. In: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 46.; REUNIÃO BRASILEIRA DE CONTROLE BIOLÓGICO, 11., 2013, Ouro Preto. [Anais...]. [Brasília]: Sociedade Brasileira de Fitopatologia, 2013. 1 CD-ROM.| Biblioteca(s): Embrapa Soja. |
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| 7. | | SOARES, R. M.; FANTINATO, G. G. P.; DARBEN, L. M.; MARCELINO-GUIMARÃES, F. C.; SEIXAS, C. D. S.; CARNEIRO, G. E. de S. First report of Curtobacterium flaccumfaciens pv. flaccumfaciens on soybean in Brazil. Tropical Plant Pathology, Brasília, DF, v. 38, n. 5, p. 452-454, Sept./Oct. 2013.| Biblioteca(s): Embrapa Soja. |
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| 8. | | CARVALHO, K. de; RINCÃO, M. P.; DARBEN, L. M.; CARVALHO, M. C. C. G. de; LOPES, I. de O. N.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C. External application of dsRNA targeting a Phakopsora pachyrhizi effector candidate attenuated fungal pathogenicity. In: INTERNATIONAL PLANT & ANIMAL GENOME CONFERENCE, 25., 2017, San Diego. Abstracts... [S. l.: s. n.], 2017. não paginado. PLANT AND ANIMAL GENOME XXV CONFERENCE - INTLPAG, 2017.| Biblioteca(s): Embrapa Soja. |
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| 9. | | POLIZEL-PODANOSQUI, A. M.; CARVALHO, M. C. C. G. de; ROCHA, C. S.; DARBEN, L. M.; LOPES-CAITAR, V. S.; AOYAOGI, L. N.; MARCELINO-GUIMARÃES, F. C. Temporal gene expression analysis of effector candidates of Phakopsora pachyrhizi across the infection cycle. In: INTERNATIONAL CONGRESS ON MOLECULAR PLANT-MICROBE INTERACTIONS, 16., 2014, Rhodes. [Abstracts...]. Atenas: International Society of Molecular Plant-Microbe Interactions, 2014.| Biblioteca(s): Embrapa Soja. |
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| 10. | | CASTANHO, F. M.; KUWAHARA, M. K.; FERNANDES, G. P.; DARBEN, L. M.; YOKOYAMA, A.; SILVA, D. C. G. da; ABDELNOOR, R. V.; MEYER, M. C.; MARCELINO-GUIMARÃES, F. C. Characterization of Phakopsora pachyrhizi races from a broad geographical and temporal collection. In: CONGRESSO BRASILEIRO DE SOJA, 9., 2022, Foz do iguaçu, PR. Desafios para a produtividade sustentável no Mercosul: resumos. Brasília, DF: Embrapa, 2022. Regina Maria Villas Bôas de Campos Leite, Adeney de Freitas Bueno, editores técnicos. resumo 105. p. 124.| Biblioteca(s): Embrapa Soja. |
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| 11. | | DARBEN, L. M.; YOKOYAMA, A.; CASTANHO, F. M.; LOPES-CAITAR, V. S.; CARVALHO, M. C. da C. G. de; GODOY, C. V.; CARVALHO, S. de; GONELA, A.; MARCELINO-GUIMARÃES, F. C. Characterization of genetic diversity and pathogenicity of Phakopsora pachyrhizi mono-uredinial isolates collected in Brazil. European Journal of Plant Pathology, v. 156, p. 355-372, 2020.| Biblioteca(s): Embrapa Soja. |
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| 12. | | CARVALHO, K.; ABE, V. Y.; DARBEN, L. M.; RINCÃO, M. P.; QI, M.; UTIYAMA, A. S.; CARVALHO, M. C. C. G.; LOPES, I. de O. N.; ABDELNOOR, R. V.; WHITHAM, S. A.; MARCELINO-GUIMARÃES, F. C. Host induced gene silencing in P. pachyrhizi effectors interfere in virulence of soybean attenuating fungal pathogenicity In: IS-MPMI Congress, 18., 2019, Glasgow. [Abstracts...]. [S. l.: s. n.], 2019.| Biblioteca(s): Embrapa Soja. |
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| 13. | | AOYAGI, L. N.; LOPES-CAITAR, V. S.; CARVALHO, M. C. C. G. de; DARBEN, L. M.; POLIZEL-PODANOSQUI, A.; KUWAHARA, M. K.; NEPOMUCENO, A. L.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C. Genomic and transcriptomic characterization of the transcription factor family R2R3-MYB in soybean and its involvement in the resistance responses to Phakopsora pachyrhizi. Plant Sciense, Limerick, v. 229, p. 32-42, Dec. 2014.| Biblioteca(s): Embrapa Soja. |
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| 14. | | KUMA, K. M.; LOPES-CAITAR, V. S.; ROMERO, C. C. T.; DARBEN, L. M.; SILVA, S. M. H.; CARVALHO, M. C. C. G. de; KUWAHARA, M. K.; OLIVEIRA, M. C. N. de; DIAS, W. P.; MARCELINO-GUIMARÃES, F. C. Functional characterization of soybean GmHsp17.6B and GmHsp22.4 genes in response to Meloidogyne javanica infection. In: WORKSHOP ON BIOTIC AND ABIOTIC STRESS TOLERANCE IN PLANTS, 2013, Ilhéus. The challenge for the 21st century: book of abstracts. [Brasília]: Embrapa: International Advanced Biology Consortium, 2013. p. 34.| Biblioteca(s): Embrapa Soja. |
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| 15. | | YOKOYAMA, A.; DARBEN, L. M.; LOPES-CAITAR, V. S.; AOYAGI, L. N.; CARVALHO, M. C. C. G. de; SOARES, R. M.; ALMEIDA, A. M. R.; MARCELINO-GUIMARÃES, F. C. Diversidade genética de isolados monouredinias de Phakopsora pachyrhizi coletados em diferentes regiões do Brasil. In: JORNADA ACADÊMICA DA EMBRAPA SOJA, 8., 2013, Londrina. Resumos expandidos... Londrina: Embrapa Soja, 2013. p. 11-15. (Embrapa Soja. Documentos, 339).| Biblioteca(s): Embrapa Soja. |
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| 16. | | DARBEN, L. M.; YOKOYAMA, A.; PARMEZAN, T. R.; KUWAHARA, M. K.; CARVALHO, M. C. C. G. de; GONELA, A.; SOARES, R. M.; ALMEIDA, A. M. R.; GODOY, C. V.; MARCELINO-GUIMARÃES, F. C. Evaluation of virulence of Phakopsora pachyrhizi monourediniais isolates collected in Brazil. In: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 47.; SIMPÓSIO BRASILEIRO DE MOFO BRANCO, 2014, Londrina. Desafios futuros: anais. Londrina: SBF, 2014. 1 CD-ROM.| Biblioteca(s): Embrapa Soja. |
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| 17. | | DARBEN, L. M.; YOKOYAMA, A.; PARMEZAN, T. R.; LOPES-CAITAR, V. S.; AOYAGI, L. N.; CARVALHO, M. C. C. G. de; GODOY, C. V.; GONELA, A.; SOARES, R. M.; ALMEIDA, A. M. R.; MARCELINO-GUIMARÃES, F. C. Molecular diversity of monouredinial Phakopsora pachyrhizi isolates collected in Brazil. In: WORKSHOP ON BIOTIC AND ABIOTIC STRESS TOLERANCE IN PLANTS, 2013, Ilhéus. The challenge for the 21st century: book of abstracts. [Brasília]: Embrapa: International Advanced Biology Consortium, 2013. p. 56.| Biblioteca(s): Embrapa Soja. |
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| 18. | | RINCÃO, M. P.; CARVALHO, M. C. da C G. de; NASCIMENTO, L. C.; LOPES-CAITAR, V. S.; CARVALHO, K. de; DARBEN, L. M.; YOKOYAMA, A.; CARAZZOLLE, M. F.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C. New insights into Phakopsora pachyrhizi infection based on transcriptome analysis in planta. Genetics and Molecular Biology, v. 41, n. 3, p. 671-691, 2018.| Biblioteca(s): Embrapa Soja. |
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| 19. | | CARVALHO, M. C. D.; NASCIMENTO, L. C.; ROCHA, C. S.; CARAZZOLE, M. F.; DARBEN, L. M.; POLIZEL-PODANOSQUI, A. M.; PEREIRA, G. A.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C. Prediction of the secretome and effectors candidates of Phakopsora pachyrhizi during the course of infection in soybean. In: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 46.; REUNIÃO BRASILEIRA DE CONTROLE BIOLÓGICO, 11., 2013, Ouro Preto. [Anais...]. [Brasília]: Sociedade Brasileira de Fitopatologia, 2013. 1 CD-ROM.| Biblioteca(s): Embrapa Soja. |
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| 20. | | CARVALHO, M. C. C. G. de; NASCIMENTO, L. C.; POLIZEL-PODANOSQUI, A. M.; ROCHA, C. S.; DARBEN, L. M.; LOPES-CAITAR, V. S.; CARAZZOLLE, M. F.; OLIVEIRA, M. L. C. S.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C. The transcriptome interactions between Phakopsora pachykopsora pachyrhizi-soybean. In: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 47.; SIMPÓSIO BRASILEIRO DE MOFO BRANCO, 2014, Londrina. Desafios futuros: anais. Londrina: SBF, 2014. 1 CD-ROM.| Biblioteca(s): Embrapa Soja. |
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| Registros recuperados : 21 | |
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Registro Completo
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
09/03/2015 |
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Data da última atualização: |
28/01/2019 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
CARVALHO, M. C. C. G. de; NASCIMENTO, L. C.; POLIZEL-PODANOSQUI, A. M.; ROCHA, C. S.; DARBEN, L. M.; LOPES-CAITAR, V. S.; CARAZZOLLE, M. F.; OLIVEIRA, M. L. C. S.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C. |
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Afiliação: |
UENP; UNICAMP; UNICAMP; UNESP; RICARDO VILELA ABDELNOOR, CNPSO; FRANCISMAR CORREA MARCELINO GUIMARA, CNPSO. |
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Título: |
The transcriptome interactions between Phakopsora pachykopsora pachyrhizi-soybean. |
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Ano de publicação: |
2014 |
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Fonte/Imprenta: |
In: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 47.; SIMPÓSIO BRASILEIRO DE MOFO BRANCO, 2014, Londrina. Desafios futuros: anais. Londrina: SBF, 2014. 1 CD-ROM. |
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Idioma: |
Inglês |
|
Conteúdo: |
The soybean rust caused by the fungus Phakopsora pachyrhizi, has caused serious damage to soybean culture since 2001 in Brazil. Several sources of rust resistance have already been identified; however no cultivar has shown stable resistance to rust. Plants are commonly infected by one or more strains of the fungus causing the breakdown of resistance acquired with the introduction of only one or a few resistance genes. In the last years, different study strategies have allowed the simultaneous monitoring of gene expression in plant-pathogen interaction, broadening our understanding of the molecular mechanisms underlying compatibility and incompatibility responses of soybean to P. pachyrhizi creating new perspectives for the development of a more durable resistance. In this work, we used laser capture microdissection (LCM) to isolate the foliar mesophyll cells of rust infection sites and access site specific processes and regulators in tolerant (compatible interaction) (BRS231) and resistant (incompatible interaction) (PI561356) soybean genotypes. RNA was extracted from the isolated cells, amplified, and sequenced with Solexa plataform. The generated paired-end sequences (54 bp) were mapped to the soybean genome and gene models (http://www.phytozome.net) for the identification of expressed genes and splicing variants. A total of 28,572 and 30,743 genes (RPKM>3) were identified for BRS231 and PI561356, respectively. The remaining reads were used to perform an ab initio assembly of P. pachyrhizi transcripts expressed at 10 dpi in planta. To improve the quality of assembly, P. pachyrhizi sequences from Sanger sequencing reads available at NCBI were trimmed and assembled into contigs and singlets. The two assemblies were merged to form PPGC1.0 comprising 36,350 unique P. pachyrhizi sequences (unisequences) expressed at 10 dpi in planta. By combining LCM with a high performance sequencing (RNA-seq) we were able to access the expression profile of a large number of genes in rust infection sites, including those related to the fungal invasion, and access new transcripts involved in soybean-rust interaction in both, compatible and incompatible interaction. Among the genes identified, the 100 soybean most expressed transcripts (RPKM) in PI561356 and BRS231 rust infection sites were stress-induced genes like cystein proteases, metallothioneins, transcription factors and genes related to protein degradation. Functional annotation of P. pachyrhizi expressed genes was done using the Blast2GO tool resulting in 3,976 transcripts associated with Gene Ontology (GO) terms, and 2,902 to biological process ontology. Biological process ontology was mainly represented by three classes of parent terms: cellular component organization or biogenesis, localization and cellular process. In the last one, two terms: response to stimulus and metabolic process were the most enriched biological process categories. Phakopsora pachyrhizi metabolic processes were strongly represented by sequences with probable function in glycogen and lipid catabolism (debranching enzymes), carbohydrate metabolism (invertases, mannitol dehydrogenases) and nitrogen metabolism (trehalose 6-phosphate synthase). Among sequences associated to response to stimulus were a great number of GO terms also linked to the symbiosis, encompassing mutualism through parasitism term (GO:0044403) including proteins involved in nucleotide binding and DNA metabolic process (nucleases and response to DNA damage stimulus), thiamin metabolic process, proteolysis, response to reactive oxygen species, GTPase mediated signal transduction, inositol-lipid mediated signaling and calmodulin signaling. Using a combination of approaches based on Blast similarities against local databases and an initio prediction, we generated a list of 905 putative secreted proteins from the total of 36,350 unique P. pachyrhizi unisequences. To identify a set of candidate P. pachyrhizi effectors, we grouped the predicted secretome into tribes or families to find those unisequences associated to expanded families. Of the 100 tribes formed, 50 of them contained more than three unisequences. A list of the 169 unisequences were obtained, that combine defining features to be common between effectors, such as small open reading frame ORF size (<250aa), no intracellular function described, enrichement of cystein residues (>3%), and presence of the previously described Y/F/WxC motif. These characteristics are mostly observed among the members of tribes 1, 2 and 17. A temporal expression of 58 candidate effector genes was characterized from spores, germinated spores and infected soybean leaves at 0, 6, 12, 24, 36, 48, 72, 96, 192 and 240 hours after inoculation (hai) using RT-qPCR. Expression analysis showed differential temporal gene expression of these candidate effectors. Heat map analysis revealed three main clusters with coordinated expression of candidates across the infection cycle. The first has candidates expressed in specific steps of infection and almost sequences have motifs common of the effectors as Y/F/WxC. Second cluster has candidates expressed during initial steps of infection that matches germ tube and appressoria formation (0 ? 24 hai) and almost sequences have ?3 cysteine residues, other common features of the effectors. Third cluster has candidates expressed only in contact with the host, suggesting that these candidates are host-induced. This last cluster has a sequence with CFEM domain associated with pathogenicity. Functional analyses are in progress with more promising candidates effectors from second and third cluster to better understand this potential effectors in soybean rust. MenosThe soybean rust caused by the fungus Phakopsora pachyrhizi, has caused serious damage to soybean culture since 2001 in Brazil. Several sources of rust resistance have already been identified; however no cultivar has shown stable resistance to rust. Plants are commonly infected by one or more strains of the fungus causing the breakdown of resistance acquired with the introduction of only one or a few resistance genes. In the last years, different study strategies have allowed the simultaneous monitoring of gene expression in plant-pathogen interaction, broadening our understanding of the molecular mechanisms underlying compatibility and incompatibility responses of soybean to P. pachyrhizi creating new perspectives for the development of a more durable resistance. In this work, we used laser capture microdissection (LCM) to isolate the foliar mesophyll cells of rust infection sites and access site specific processes and regulators in tolerant (compatible interaction) (BRS231) and resistant (incompatible interaction) (PI561356) soybean genotypes. RNA was extracted from the isolated cells, amplified, and sequenced with Solexa plataform. The generated paired-end sequences (54 bp) were mapped to the soybean genome and gene models (http://www.phytozome.net) for the identification of expressed genes and splicing variants. A total of 28,572 and 30,743 genes (RPKM>3) were identified for BRS231 and PI561356, respectively. The remaining reads were used to perform an ab initio assembly... Mostrar Tudo |
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Thesagro: |
Doença de Planta; Ferrugem; Soja. |
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Thesaurus NAL: |
Plant diseases and disorders; Soybean rust; Soybeans. |
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Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/119824/1/PALESTRA18.pdf
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Marc: |
LEADER 06688nam a2200289 a 4500
001 2010927
005 2019-01-28
008 2014 bl uuuu u00u1 u #d
100 1 $aCARVALHO, M. C. C. G. de
245 $aThe transcriptome interactions between Phakopsora pachykopsora pachyrhizi-soybean.$h[electronic resource]
260 $aIn: CONGRESSO BRASILEIRO DE FITOPATOLOGIA, 47.; SIMPÓSIO BRASILEIRO DE MOFO BRANCO, 2014, Londrina. Desafios futuros: anais. Londrina: SBF, 2014. 1 CD-ROM.$c2014
520 $aThe soybean rust caused by the fungus Phakopsora pachyrhizi, has caused serious damage to soybean culture since 2001 in Brazil. Several sources of rust resistance have already been identified; however no cultivar has shown stable resistance to rust. Plants are commonly infected by one or more strains of the fungus causing the breakdown of resistance acquired with the introduction of only one or a few resistance genes. In the last years, different study strategies have allowed the simultaneous monitoring of gene expression in plant-pathogen interaction, broadening our understanding of the molecular mechanisms underlying compatibility and incompatibility responses of soybean to P. pachyrhizi creating new perspectives for the development of a more durable resistance. In this work, we used laser capture microdissection (LCM) to isolate the foliar mesophyll cells of rust infection sites and access site specific processes and regulators in tolerant (compatible interaction) (BRS231) and resistant (incompatible interaction) (PI561356) soybean genotypes. RNA was extracted from the isolated cells, amplified, and sequenced with Solexa plataform. The generated paired-end sequences (54 bp) were mapped to the soybean genome and gene models (http://www.phytozome.net) for the identification of expressed genes and splicing variants. A total of 28,572 and 30,743 genes (RPKM>3) were identified for BRS231 and PI561356, respectively. The remaining reads were used to perform an ab initio assembly of P. pachyrhizi transcripts expressed at 10 dpi in planta. To improve the quality of assembly, P. pachyrhizi sequences from Sanger sequencing reads available at NCBI were trimmed and assembled into contigs and singlets. The two assemblies were merged to form PPGC1.0 comprising 36,350 unique P. pachyrhizi sequences (unisequences) expressed at 10 dpi in planta. By combining LCM with a high performance sequencing (RNA-seq) we were able to access the expression profile of a large number of genes in rust infection sites, including those related to the fungal invasion, and access new transcripts involved in soybean-rust interaction in both, compatible and incompatible interaction. Among the genes identified, the 100 soybean most expressed transcripts (RPKM) in PI561356 and BRS231 rust infection sites were stress-induced genes like cystein proteases, metallothioneins, transcription factors and genes related to protein degradation. Functional annotation of P. pachyrhizi expressed genes was done using the Blast2GO tool resulting in 3,976 transcripts associated with Gene Ontology (GO) terms, and 2,902 to biological process ontology. Biological process ontology was mainly represented by three classes of parent terms: cellular component organization or biogenesis, localization and cellular process. In the last one, two terms: response to stimulus and metabolic process were the most enriched biological process categories. Phakopsora pachyrhizi metabolic processes were strongly represented by sequences with probable function in glycogen and lipid catabolism (debranching enzymes), carbohydrate metabolism (invertases, mannitol dehydrogenases) and nitrogen metabolism (trehalose 6-phosphate synthase). Among sequences associated to response to stimulus were a great number of GO terms also linked to the symbiosis, encompassing mutualism through parasitism term (GO:0044403) including proteins involved in nucleotide binding and DNA metabolic process (nucleases and response to DNA damage stimulus), thiamin metabolic process, proteolysis, response to reactive oxygen species, GTPase mediated signal transduction, inositol-lipid mediated signaling and calmodulin signaling. Using a combination of approaches based on Blast similarities against local databases and an initio prediction, we generated a list of 905 putative secreted proteins from the total of 36,350 unique P. pachyrhizi unisequences. To identify a set of candidate P. pachyrhizi effectors, we grouped the predicted secretome into tribes or families to find those unisequences associated to expanded families. Of the 100 tribes formed, 50 of them contained more than three unisequences. A list of the 169 unisequences were obtained, that combine defining features to be common between effectors, such as small open reading frame ORF size (<250aa), no intracellular function described, enrichement of cystein residues (>3%), and presence of the previously described Y/F/WxC motif. These characteristics are mostly observed among the members of tribes 1, 2 and 17. A temporal expression of 58 candidate effector genes was characterized from spores, germinated spores and infected soybean leaves at 0, 6, 12, 24, 36, 48, 72, 96, 192 and 240 hours after inoculation (hai) using RT-qPCR. Expression analysis showed differential temporal gene expression of these candidate effectors. Heat map analysis revealed three main clusters with coordinated expression of candidates across the infection cycle. The first has candidates expressed in specific steps of infection and almost sequences have motifs common of the effectors as Y/F/WxC. Second cluster has candidates expressed during initial steps of infection that matches germ tube and appressoria formation (0 ? 24 hai) and almost sequences have ?3 cysteine residues, other common features of the effectors. Third cluster has candidates expressed only in contact with the host, suggesting that these candidates are host-induced. This last cluster has a sequence with CFEM domain associated with pathogenicity. Functional analyses are in progress with more promising candidates effectors from second and third cluster to better understand this potential effectors in soybean rust.
650 $aPlant diseases and disorders
650 $aSoybean rust
650 $aSoybeans
650 $aDoença de Planta
650 $aFerrugem
650 $aSoja
700 1 $aNASCIMENTO, L. C.
700 1 $aPOLIZEL-PODANOSQUI, A. M.
700 1 $aROCHA, C. S.
700 1 $aDARBEN, L. M.
700 1 $aLOPES-CAITAR, V. S.
700 1 $aCARAZZOLLE, M. F.
700 1 $aOLIVEIRA, M. L. C. S.
700 1 $aABDELNOOR, R. V.
700 1 $aMARCELINO-GUIMARÃES, F. C.
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