Abstract

GRAS genes are suggested to be grouped into plant-specific transcriptional regulatory families that have been reported to participate in multiple processes, including plant development, phytohormone signaling, the formation of symbiotic relationships, and response to environmental signals. GRAS genes have been characterized in a number of plant species, but little is known about this gene family in Citrus sinensis. In this study, we identified a total of 50 GRAS genes and characterized the gene structures, conserved motifs, genome localizations and cis-elements within their promoter regions. According to their structural and phylogenetic features, the identified sweet orange GRAS members were divided into 11 subgroups, of which subfamily CsGRAS34 was sweet orange-specific. Based on publicly available RNA-seq data generated from callus, flower, leaf and fruit in sweet orange, we found that some sweet orange GRAS genes exhibited tissue-specific expression patterning. Three of the six members of subfamily AtSHR, particularly CsGRAS9, and two of the six members of subfamily AtPAT1 were preferentially expressed in leaf. Moreover, protein-protein interactions with CsGRAS were predicted. Gene expression analysis was performed under conditions of phosphate deficiency, and GA3 and NaCl treatment to identify the potential functions of GRAS members in regulating stress and hormone responses. This study provides the first comprehensive understanding of the GRAS gene family in the sweet orange genome. As such, the study generates valuable information for further gene function analysis and identifying candidate genes to improve abiotic stress tolerance in citrus plants.

Highlights

  • C. sinensis is an extremely important fruit crop in many countries

  • SCL14 serves as a transcriptional coactivator of TGA transcription factors and regulates the induction of genes involved in the detoxification of harmful chemicals[38]

  • CsGRAS14, Os19 family member, possibly participates in brassinosteroid-signaling[24]. These results suggested the potential function of CsGRAS proteins which may have similar roles to other GRAS proteins of rice and Arabidopsis in the same subfamilies

Read more

Summary

Introduction

C. sinensis is an extremely important fruit crop in many countries. The release of the whole-genome sequence of sweet orange provides an opportunity to comprehensively analyze numerous known gene families[1,2]. The intrinsically disordered N-terminal regions are likely responsible for the specific function of each GRAS gene[5]. AtSCL3 (scarecrow like 3) is a positive regulator of the GA response pathway[21]. DLT (dwarf and low-tillering) and OsGRAS19 act as positive regulators in brassinosteroid signaling in rice[23,24]. SCL21 (SCARECROW-LIKE21) and PAT1 (PHYTOCHROME A SIGNAL TRANSDUCTION1) are positive regulators of phytochrome A (phyA) signal transduction for several high-irradiance responses[35,36]. OsGRAS23, a rice GRAS transcription factor, positively regulates rice drought tolerance via the induction of a number of stress-responsive genes[40]. PeSCL7, a poplar GRAS/SCL gene, is induced by drought and high salt, and repressed by gibberellic acid (GA) treatment. Compared with wide-type plant, Arabidopsis overexpressing PeSCL7 shows higher tolerance to drought and salt treatment[2]

Methods
Findings
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call