RESUMO
Mlo gene encodes a plant-specific seven-transmembrane domain protein involved in a variety of cellular processes. In this study, a novel Mlo gene from rubber tree (Hevea brasiliensis), designated HbMlo1, was cloned by RT-PCR in rubber tree. The ORF of HbMlo1 was 1551bp in length, encoding a putative protein of 516 amino acids. HbMlo1 was a typical Mlo protein with seven-transmembrane domain. Sequence comparison between HbMlo1 and other Mlo proteins demonstrated that HbMlo1 shared the highest similarity with the Cucumis melo CmMlo1 and Arabidopsis thaliana AtMlo1 with 75.1% and 71.3% sequence identity, respectively. Phylogenetic analysis revealed that HbMlo1, CmMlo1, AtMlo1, AtMlo13, and AtMlo15 formed into the phylogenetic clade II with 100% bootstrap support value. HbMlo1 transcript exhibited tissue specificity, and it was preferentially expressed in leaf. Furthermore, the amount of HbMlo1 transcript was significantly induced by various phytohormones (including ethephon, methyl jasmonate, salicylic acid, abscisic acid, indole-3-acetic acid, and gibberellic acid), H2O2, and wounding treatments. Under drought stress, HbMlo1 exhibited a complex pattern of regulation. However, HbMlo1 expression did not significantly change during powdery mildew infection. These results suggested that HbMlo1 might play a role in phytohormone signaling and abiotic stress response processes in rubber tree.
Assuntos
Regulação da Expressão Gênica de Plantas , Hevea/enzimologia , Reguladores de Crescimento de Plantas/farmacologia , Transdução de Sinais , Sequência de Aminoácidos , Clonagem Molecular , Hevea/genética , Hevea/fisiologia , Peróxido de Hidrogênio/metabolismo , Dados de Sequência Molecular , Especificidade de Órgãos , Filogenia , Folhas de Planta/enzimologia , Folhas de Planta/genética , Folhas de Planta/fisiologia , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Alinhamento de Sequência , Estresse FisiológicoRESUMO
The Rad6 gene of Saccharomyces cerevisiae encodes an ubiquitin-conjugating enzyme (E2) which is required for DNA repair, damage-induced mutagenesis, sporulation, etc. In this study, one Rad6 homolog, designated HbRad6, was cloned in rubber tree (Hevea brasiliensis). The putative protein sequence of HbRad6 contains 152 amino acids, a conserved UBC domain, and a conserved active-site cysteine in the UBC domain, which is required for E2 enzymes catalytic activity. HbRad6 shared high similarity with Rad6 from other species. It shared the highest similarity with rice OsRad6 and Arabidopsis thaliana AtUBC2 with 96.05% identical residues, and 63.16% sequence identity with yeast Rad6 (excluding the acidic tail). Comparing expression among different Hevea tissues demonstrated that HbRad6 was ubiquitously expressed in all tissues, but it revealed a preferential expression in the latex. Furthermore, HbRad6 expression was markedly induced by DNA-damaging agent H2O2, the latex stimulator ethephon (ET), and methyl jasmonate (MeJA), while NaCl and wounding treatments had relatively minor effect upon its expression. Genetic complementation experiment revealed that HbRad6 had minor effects on the complementation of the UV sensitivity of yeast rad6 null mutant, indicating that the Hevea Rad6 protein may partially suppress the UV sensitivity of the yeast rad6 mutant. These results suggested that HbRad6 was a multifunction gene involved in DNA damage repair, hormones and stress responses in rubber tree.
Assuntos
Reparo do DNA , Genes de Plantas , Hevea/genética , Proteínas de Saccharomyces cerevisiae/metabolismo , Saccharomyces cerevisiae/genética , Enzimas de Conjugação de Ubiquitina/metabolismo , Acetatos/farmacologia , Sequência de Aminoácidos , Clonagem Molecular , Ciclopentanos/farmacologia , Dano ao DNA , Evolução Molecular , Regulação da Expressão Gênica/efeitos dos fármacos , Teste de Complementação Genética , Hevea/metabolismo , Peróxido de Hidrogênio/farmacologia , Compostos Organofosforados/farmacologia , Oxilipinas/farmacologia , Filogenia , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Saccharomyces cerevisiae/metabolismo , Proteínas de Saccharomyces cerevisiae/genética , Alinhamento de Sequência , Cloreto de Sódio/farmacologia , Estresse Mecânico , Enzimas de Conjugação de Ubiquitina/genética , Raios UltravioletaRESUMO
The translationally controlled tumor protein (TCTP) is a multi-functioning protein that carries out vital roles in various life processes. In this study, a new TCTP gene, designated as HbTCTP1, was isolated in Hevea brasiliensis. The full-length complementary DNA (cDNA) of HbTCTP1 contained a maximum open reading frame (ORF) of 507base pair (bp) encoding 168 amino acids. The sequence comparison showed that the deduced HbTCTP1 indicated high identities to plant TCTP proteins, and clustered in the dicot cluster of plant TCTPs. Although HbTCTP1 and human TCTP proteins did not parallel in overall sequence similarity, they indicated highly similar 3D structures with a nearly identical spatial organization of α-helices, ß-sheets, and coil regions. Real time reverse-transcription PCR (RT-PCR) analyses showed that HbTCTP1 was expressed throughout different tissues and developmental stages of leaves. Besides being related to tapping panel dryness (TPD), the HbTCTP1 transcripts were regulated by various treatments, including drought, low temperature, high salt, ethrel (ET), wounding, H2O2, and methyl jasmonate (Me-JA) treatments. The recombinant HbTCTP1 fusion protein was shown to protect supercoiled plasmid DNA from damages induced by metal-catalyzed generation of reactive oxygen species. The (45)Ca(2+)-overlay assay showed that HbTCTP1 was a calcium-binding protein. Our results are greatly helpful in understanding the molecular characterization and expression profiles of HbTCTP1, and lay the foundation for further analyzing the function of HbTCTP1 in rubber tree.
Assuntos
Biomarcadores Tumorais/genética , Perfilação da Expressão Gênica , Regulação da Expressão Gênica de Plantas , Hevea/genética , Borracha/metabolismo , Sequência de Bases , Biomarcadores Tumorais/química , Biomarcadores Tumorais/metabolismo , Proteínas de Ligação ao Cálcio/metabolismo , Clonagem Molecular , DNA Complementar/genética , DNA Super-Helicoidal/metabolismo , Humanos , Dados de Sequência Molecular , Proteínas de Plantas/química , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Reação em Cadeia da Polimerase em Tempo Real , Proteínas Recombinantes de Fusão/isolamento & purificação , Proteínas Recombinantes de Fusão/metabolismo , Análise de Sequência de DNA , Proteína Tumoral 1 Controlada por TraduçãoRESUMO
BACKGROUND: In rubber tree, bark is one of important agricultural and biological organs. However, the molecular mechanism involved in the bark formation and development in rubber tree remains largely unknown, which is at least partially due to lack of bark transcriptomic and genomic information. Therefore, it is necessary to carried out high-throughput transcriptome sequencing of rubber tree bark to generate enormous transcript sequences for the functional characterization and molecular marker development. RESULTS: In this study, more than 30 million sequencing reads were generated using Illumina paired-end sequencing technology. In total, 22,756 unigenes with an average length of 485 bp were obtained with de novo assembly. The similarity search indicated that 16,520 and 12,558 unigenes showed significant similarities to known proteins from NCBI non-redundant and Swissprot protein databases, respectively. Among these annotated unigenes, 6,867 and 5,559 unigenes were separately assigned to Gene Ontology (GO) and Clusters of Orthologous Group (COG). When 22,756 unigenes searched against the Kyoto Encyclopedia of Genes and Genomes Pathway (KEGG) database, 12,097 unigenes were assigned to 5 main categories including 123 KEGG pathways. Among the main KEGG categories, metabolism was the biggest category (9,043, 74.75%), suggesting the active metabolic processes in rubber tree bark. In addition, a total of 39,257 EST-SSRs were identified from 22,756 unigenes, and the characterizations of EST-SSRs were further analyzed in rubber tree. 110 potential marker sites were randomly selected to validate the assembly quality and develop EST-SSR markers. Among 13 Hevea germplasms, PCR success rate and polymorphism rate of 110 markers were separately 96.36% and 55.45% in this study. CONCLUSION: By assembling and analyzing de novo transcriptome sequencing data, we reported the comprehensive functional characterization of rubber tree bark. This research generated a substantial fraction of rubber tree transcriptome sequences, which were very useful resources for gene annotation and discovery, molecular markers development, genome assembly and annotation, and microarrays development in rubber tree. The EST-SSR markers identified and developed in this study will facilitate marker-assisted selection breeding in rubber tree. Moreover, this study also supported that transcriptome analysis based on Illumina paired-end sequencing is a powerful tool for transcriptome characterization and molecular marker development in non-model species, especially those with large and complex genomes.