Abstract

BackgroundTranscription factors of the basic leucine zipper (bZIP) family represent exclusively in eukaryotes and have been shown to regulate diverse biological processes in plant growth and development as well as in abiotic and biotic stress responses. However, little is known about the bZIP family in tomato (Solanum lycopersicum L.).MethodsThe SlbZIP genes were identified using local BLAST and hidden Markov model profile searches. The phylogenetic trees, conserved motifs and gene structures were generated by MEGA6.06, MEME tool and gene Structure Display Server, respectively. The syntenic block diagrams were generated by the Circos software. The transcriptional gene expression profiles were obtained using Genevestigator tool and quantitative RT-PCR.ResultsIn the present study, we carried out a genome-wide identification and systematic analyses of 69 SlbZIP genes that distributes unevenly on the tomato chromosomes. This family can be divided into 9 groups according to the phylogenetic relationship among the SlbZIP proteins. Six kinds of intron patterns (a–f) within the basic and hinge regions are defined. The additional conserved motifs and their presence of the group specificity were also identified. Further, we predicted the DNA-binding patterns and the dimerization property on the basis of the characteristic features in the basic and hinge regions and the leucine zipper, respectively, which supports our classification greatly and helps to classify 24 distinct subfamilies. Within the SlbZIP family, a total of 40 SlbZIP genes are located in the segmental duplicate regions in the tomato genome, suggesting that the segment chromosomal duplications contribute greatly to the expansion of the tomato SlbZIP family. Expression profiling analyses of 59 SlbZIP genes using quantitative RT-PCR and publicly available microarray data indicate that the tomato SlbZIP genes have distinct and diverse expression patterns in different tissues and developmental stages and many of the tomato bZIP genes might be involved in responses to various abiotic and biotic stresses as well as in response to light.ConclusionsThis genome-wide systematic characterization identified a total of 69 members in the SlbZIP family and the analyses of the protein features and gene expression patterns provide useful clues for further functional characterization of the bZIP transcription factors in tomato.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1990-6) contains supplementary material, which is available to authorized users.

Highlights

  • Transcription factors of the basic leucine zipper family represent exclusively in eukaryotes and have been shown to regulate diverse biological processes in plant growth and development as well as in abiotic and biotic stress responses

  • The basic leucine zipper (bZIP) Transcription factors (TFs) are named according to their common feature, bZIP domain, which consists of ∼ 60–80 amino acids in length, surrounded by two functionally distinct regions, a basic region and a Leu zipper [1]

  • Characterization and nomenclature of the SlbZIP family Based on an extensive survey against tomato genome database using the conserved bZIP domain sequence as a BLASTP query, a total of 104 putative SlbZIP candidates were initially obtained with the E-value threshold of 1.0

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Summary

Methods

Plant growth conditions and treatments Tomato (Solanum lycopersicum) cv. Suhong 2003 was used for all gene expression analysis by qRT-PCR. Transactivation activity and subcellular localization assays For transactivation activity assays, the entire coding sequences of SlbZIP06, SlbZIP12, SlbZIP16, SlbZIP32 and SlbZIP46 were amplified using gene-specific primers (Additional file 12: Table S7) and fused in frame to the yeast GAL4 DNA binding domain in vector pBDGAL4Cam with corresponding restriction enzymes, yielding plasmid pBD-SlbZIP06, pBD-SlbZIP12, pBDSlbZIP16, pBD-SlbZIP32 and pBD-SlbZIP46, respectively. These plasmids and pBD empty vector (negative control) were transformed into yeast strain AH109.

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