Abstract

Heat shock protein 70s (HSP70s) are highly conserved proteins that are involved in stress responses. These chaperones play pivotal roles in protein folding, removing the extra amounts of oxidized proteins, preventing protein denaturation, and improving the antioxidant system activities. This conserved family has been characterized in several crops under drought stress conditions. However, there is no study on HSP70s in pumpkin (Cucurbita moschata). Therefore, we performed a comprehensive analysis of this gene family, including phylogenetic relationship, motif and gene structure analysis, gene duplication, collinearity, and promoter analysis. In this research, we found 21 HSP70s that were classified into five groups (from A to E). These genes were mostly localized in the cytoplasm, chloroplast, mitochondria, nucleus, and endoplasmic reticulum (ER). We could observe more similarity in closely linked subfamilies in terms of motifs, the number of introns/exons, and the corresponding cellular compartments. According to the collinearity analysis, gene duplication had occurred as a result of purifying selection. The results showed that the occurrence of gene duplication for all nine gene pairs was due to segmental duplication (SD). Synteny analysis revealed a closer relationship between pumpkin and cucumber than pumpkin and Arabidopsis. Promoter analysis showed the presence of various cis-regulatory elements in the up-stream region of the HSP70 genes, such as hormones and stress-responsive elements, indicating a potential role of this gene family in stress tolerance. We furtherly performed the gene expression analysis of the HSP70s in pumpkin under progressive drought stress. Pumpkin is widely used as a rootstock to improve stress tolerance, as well as fruit quality of cucumber scion. Since stress-responsive mobile molecules translocate through vascular tissue from roots to the whole plant body, we used the xylem of grafted materials to study the expression patterns of the HSP70 (potentially mobile) gene family. The results indicated that all CmoHSP70s had very low expression levels at 4 days after stress (DAS). However, the genes showed different expression patterns by progressing he drought period. For example, the expression of CmoHSP70-4 (in subgroup E) and CmoHSP70-14 (in subgroup C) sharply increased at 6 and 11 DAS, respectively. However, the expression of all genes belonging to subgroup A did not change significantly in response to drought stress. These findings indicated the diverse roles of this gene family under drought stress and provided valuable information for further investigation on the function of this gene family, especially under stressful conditions.

Highlights

  • Environmental threats are becoming more serious because of climate change and global warming [1]

  • We could mine 21 Heat shock protein 70s (HSP70s) genes in C. moschata based on the BLASTP method using the domain sequence of Arabidopsis HSP70 as the query

  • Genome-wide identification of CmoHSP70s in pumpkin revealed that there are 21 genes in this gene family that are unevenly distributed on pumpkin chromosomes

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Summary

Introduction

Environmental threats are becoming more serious because of climate change and global warming [1]. Evolutionary analysis has shown that plants have more stress-responsive genes, such as heat shock proteins (HSPs), than other organisms as a result of whole-genome duplications to cope with adverse conditions [3]. HSP70s, which are highly conserved in prokaryotes (DnaK) and eukaryotes (HSP70) [6,7], play dominant roles in plant development. These chaperones have various functions, such as assisting proteins in correct folding, protecting proteins against misfolding [8], repairing the damaged proteins, and removing the extra amounts of damaged proteins to avoid oxidative stress [9]. There are three conserved domains in this gene family, including C-terminal substrate binding domain, or SBD (about 10 kDa for biding to the substrate), intermediate domain

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