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BACKGROUND: bZIP proteins participate in the regulation of gene expression, playing crucial roles in various biological processes in plants, including response to environmental changes. Luminosity is an environmental factor of extreme importance for plant metabolism, acting as a regulator of its growth and development. Despite advances in the identification of bZIP proteins in several plant species, studies on these transcription factors in cassava are lacking. Cassava (Manihot esculenta Crantz) is one of the most important food crops in tropical and subtropical regions, mainly in developing countries, where its storage root is a major source of calories for low-income people. OBJECTIVES: Our main aim was the isolation of a cDNA sequence encoding a bZIP protein from cassava (MebZIP) as well as the in silico characterization of its nucleotide and deduced amino acid sequences. In addition, we evaluated the expression pattern of the MebZIP gene in response to light, and its possible relationship with regulation of the chalcone synthase (MeCHS) gene. METHODS: RT-PCR and 3' and 5' RACE assays were used to isolate the full-length cDNA sequence of MebZIP. Bioinformatics tools were used to characterize the nucleotide and amino acid sequences of MebZIP. Semiquantitative RT-PCR assays were used to evaluate the expression levels of MebZIP and MeCHS genes. RESULTS: We isolated the full-length cDNA sequence of MebZIP with a 1320-bp ORF encoding a deduced protein with a predicted molecular weight and isoelectric point of 47 kDa and 5.85, respectively. Comparative analyses with GenBank sequences showed high identity of MebZIP with bZIP CPRF-2 of Hevea brasiliensis (XP_021650934) and Petroselinum crispum (Q99090.2). Besides the basic region and leucine zipper domains, MebZIP contains putative conserved domains (D1- D4), found in parsley CPRF-2 and bZIP proteins closely related to this protein. Since CPRF proteins are known for their function in regulation of the CHS gene by light, we evaluated the expression levels of the MebZIP gene and the possible target gene to be regulated by MebZIP (the MeCHS gene) in cassava under light conditions. Semi-quantitative RT-PCR assays revealed that MebZIP transcription increased in response to white light, with maximum expression levels at 6 h of light exposure. On the other hand, the expression levels of the MeCHS gene were statistically constant in all samples, indicating that they were not influenced by the experimental conditions used here. CONCLUSION: The putative MebZIP protein identified in this work contains the conserved domains (bZIP, D1-D4) that indicate its functionality, thus allowing it to be considered a new member of the bZIP transcription factor CPRF-2 family. The expression levels of the MebZIP gene increased during white light exposure, indicating a potential function in light-response in cassava.

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ABSTRACT The bacurizeiro (Platonia insignis Mart.) is a tree native to the Amazon whose fruit is much used in the gastronomy in the North and Northeast regions of Brazil. Due to its great economic potential for these regions, the species is being conserved in germplasm banks to support genetic breeding programs. The aim of this work was the molecular characterization of P. insignis accessions belonging to the germplasm bank of the Embrapa Eastern Amazon research unit using ISSR (Inter Simple Sequence Repeat) markers. Seventy-eight accessions of P. insignis belonging to 16 progenies were sampled in two different localities on Marajó Island, state of Pará, Brazil. Among the 16 progenies, seven were collected in Soure and nine in Salvaterra. The 78 accessions were genotyped with 23 pre-selected primers. We obtained 121 amplified products, of which 54 were polymorphic. The most polymorphic primers were UBC 834, UBC 899 and UBC 900. Primers UBC810 and UBC884 did not amplify polymorphic bands. Forty-nine markers out of 54 were selected for genetic analyses. AMOVA within and among progenies showed low genetic differentiation (PT = 0.064, P 0.001) with higher diversity within progenies (96%), low genetic differentiation among sampling localities (PT = 0.025, P 0.013), and higher diversity within (98%) than among localities. Clustering by UPGMA based on Jaccard similarities among pairs of accessions did not separate genotypes according to progeny or sampling localitiy. We recommend that new germplasm surveys consider a greater sampling effort within sampling localitites.(AU)

RESUMO O bacurizeiro (Platonia insignis Mart.) é uma espécie frutífera nativa da Amazônia muito utilizada na cultura alimentar nas regiões Norte e Nordeste do Brasil. Devido a seu grande potencial econômico regional, a espécie vem sendo conservada em bancos ativos de germoplasma (BAG) para apoiar programas de melhoramento genético. Dessa forma, o objetivo deste trabalho foi caracterizar molecularmente acessos de P. insignis pertencentes ao BAG da Embrapa Amazônia Oriental por meio de marcadores ISSR (Inter Simple Sequence Repeat). Foram coletados 78 acessos de P. insignis pertencentes a 16 progênies coletadas em dois locais diferentes na Ilha de Marajó, PA. Das 16 progênies, sete foram coletadas em Soure e nove em Salvaterra. Os 78 acessos foram genotipados com 23 primers ISSR pré-selecionados. Obteve-se 121 produtos amplificados, dos quais 54 foram polimórficos. Os primers mais polimórficos foram UBC 834, UBC 899 e UBC 900. Já os primers UBC810 e UBC884 não apresentaram bandas polimórficas. Das 54 marcas, 49 foram selecionadas para as análises genéticas. A AMOVA entre e dentro de progênies identificou baixa diferenciação genética (PT = 0,064, P 0,001) com maior diversidade dentro de progênies (96%), bem como baixa diferenciação genética entre os locais de coleta (PT = 0,025, P 0,013), com maior diversidade dentro (98%) do que entre locais. O agrupamento pelo método UPGMA, com base nas similaridades de Jaccard entre os acessos, não separou as amostras por progênie ou local de coleta. Recomenda-se que novas coletas de germoplasma considerem maior esforço de coleta em cada local amostrado.(AU)

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RESUMO

ABSTRACT The bacurizeiro (Platonia insignis Mart.) is a tree native to the Amazon whose fruit is much used in the gastronomy in the North and Northeast regions of Brazil. Due to its great economic potential for these regions, the species is being conserved in germplasm banks to support genetic breeding programs. The aim of this work was the molecular characterization of P. insignis accessions belonging to the germplasm bank of the Embrapa Eastern Amazon research unit using ISSR (Inter Simple Sequence Repeat) markers. Seventy-eight accessions of P. insignis belonging to 16 progenies were sampled in two different localities on Marajó Island, state of Pará, Brazil. Among the 16 progenies, seven were collected in Soure and nine in Salvaterra. The 78 accessions were genotyped with 23 pre-selected primers. We obtained 121 amplified products, of which 54 were polymorphic. The most polymorphic primers were UBC 834, UBC 899 and UBC 900. Primers UBC810 and UBC884 did not amplify polymorphic bands. Forty-nine markers out of 54 were selected for genetic analyses. AMOVA within and among progenies showed low genetic differentiation (ΦPT = 0.064, P<0.001) with higher diversity within progenies (96%), low genetic differentiation among sampling localities (ΦPT = 0.025, P<0.013), and higher diversity within (98%) than among localities. Clustering by UPGMA based on Jaccard similarities among pairs of accessions did not separate genotypes according to progeny or sampling localitiy. We recommend that new germplasm surveys consider a greater sampling effort within sampling localitites.

RESUMO O bacurizeiro (Platonia insignis Mart.) é uma espécie frutífera nativa da Amazônia muito utilizada na cultura alimentar nas regiões Norte e Nordeste do Brasil. Devido a seu grande potencial econômico regional, a espécie vem sendo conservada em bancos ativos de germoplasma (BAG) para apoiar programas de melhoramento genético. Dessa forma, o objetivo deste trabalho foi caracterizar molecularmente acessos de P. insignis pertencentes ao BAG da Embrapa Amazônia Oriental por meio de marcadores ISSR (Inter Simple Sequence Repeat). Foram coletados 78 acessos de P. insignis pertencentes a 16 progênies coletadas em dois locais diferentes na Ilha de Marajó, PA. Das 16 progênies, sete foram coletadas em Soure e nove em Salvaterra. Os 78 acessos foram genotipados com 23 primers ISSR pré-selecionados. Obteve-se 121 produtos amplificados, dos quais 54 foram polimórficos. Os primers mais polimórficos foram UBC 834, UBC 899 e UBC 900. Já os primers UBC810 e UBC884 não apresentaram bandas polimórficas. Das 54 marcas, 49 foram selecionadas para as análises genéticas. A AMOVA entre e dentro de progênies identificou baixa diferenciação genética (ΦPT = 0,064, P<0,001) com maior diversidade dentro de progênies (96%), bem como baixa diferenciação genética entre os locais de coleta (ΦPT = 0,025, P<0,013), com maior diversidade dentro (98%) do que entre locais. O agrupamento pelo método UPGMA, com base nas similaridades de Jaccard entre os acessos, não separou as amostras por progênie ou local de coleta. Recomenda-se que novas coletas de germoplasma considerem maior esforço de coleta em cada local amostrado.

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