Abstract

The GATA gene family is one of the most important transcription factors (TFs). It extensively exists in plants, contributes to diverse biological processes such as the development process, and responds to environmental stress. Although the GATA gene family has been comprehensively and systematically studied in many species, less is known about GATA genes in Chinese pears (Pyrus bretschneideri). In the current study, the GATA gene family in the four Rosaceae genomes was identified, its structural characteristics identified, and a comparative analysis of its properties was carried out. Ninety-two encoded GATA proteins were authenticated in the four Rosaceae genomes (Pyrus bretschneideri, Prunus avium, Prunus mume, and Prunus persica) and categorized into four subfamilies (Ⅰ–Ⅳ) according to phylogeny. The majority of GATA genes contained one to two introns and conserved motif composition analysis revealed their functional divergence. Whole-genome duplications (WGDs) and dispersed duplication (DSD) played a key role in the expansion of the GATA gene family. The microarray indicated that, among P. bretschneideri, P. avium, P. mume and P. persica, GATA duplicated regions were more conserved between Pyrus bretschneideri and Prunus persica with 32 orthologous genes pairs. The physicochemical parameters, duplication patterns, non-synonymous (ka), and synonymous mutation rate (ks) and GO annotation ontology were performed using different bioinformatics tools. cis-elements respond to various phytohormones, abiotic/biotic stress, and light-responsive were found in the promoter regions of GATA genes which were induced via stimuli. Furthermore, subcellular localization of the PbGATA22 gene product was investigated, showing that it was present in the nucleus of tobacco (Nicotiana tabacum) epidermal cells. Finally, in silico analysis was performed on various organs (bud, leaf, stem, ovary, petal, and sepal) and different developmental stages of fruit. Subsequently, the expression profiles of PbGATA genes were extensively expressed under exogenous hormonal treatments of SA (salicylic acid), MeJA (methyl jasmonate), and ABA (abscisic acid) indicating that play important role in hormone signaling pathways. A comprehensive analysis of GATA transcription factors was performed through systematic biological approaches and comparative genomics to establish a theoretical base for further structural and functional investigations in Rosaceae species.

Highlights

  • Transcription factors (TFs) are a major component that regulates gene expression by binding to the gene’s promoter and controlling various biological processes

  • A total of 92 GATA members were investigated from four Rosaceae species with 32 from Pyrus bretschneideri (PbGATA1-PbGATA32), 18 from Prunus avium (PaGATA1-PaGATA18), 20 proteins from Prunus mume (PmGATA1PmGATA20), and 22 from Prunus persica (PpGATA1-PpGATA22)

  • The evolutionary relationship was investigated between four Rosaceae species (Pyrus bretschneideri, Prunus avium, Prunus mume, and Prunus persica)

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Summary

Introduction

Transcription factors (TFs) are a major component that regulates gene expression by binding to the gene’s promoter and controlling various biological processes. GATA transcription factors are distinguished by their ability to bind the W-GA-TA-R (W = T/A, R = G/A) sequences on the promoter regions [6]. The function of GATA transcription factors in animals and fungi has been extensively investigated [8,9,10] while in plants, GATA transcription factors are directly implicated in the regulation of stress signaling and metabolic pathways in addition to their active role in cell differentiation [11,12]. GATA transcription factors execute several functions in fungal cells, including siderophore formation, circadian regulation, and nitrogen metabolism [13,14]. NTL1 is a homolog of NIT-2, the first plant GATA transcription factor discovered in tobacco which plays a key role in nitrogen metabolism [15].

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