Gangzheng Wang1,2†Yi Luo1†Chen Wang1Yan Zhou1Chunye Mou1Heng Kang1Yang Xiao1
Yinbing Bian1
Yu Hua Gong1*- 1Institute of Applied Mycology, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
- 2State Key Laboratory of Applied Microbiology Southern China, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangdong Institute of Microbiology, Guangzhou, China
Our previous study found that LeDnaJ07 RNAi decreased Lentinula edodes resistance to heat stress and Trichoderma atroviride infection. In this study, the structure and function of the LeDnaJ07 gene was analyzed by gene cloning and overexpression in L. edodes stress-sensitive strain YS55 via the Agrobacterium-mediated transformation method. Transformants were confirmed by qRT-PCR, fluorescence observation and Southern blotting. Overexpression of LeDnaJ07 in YS55 not only enhanced L. edodes mycelial resistance to heat stress but also facilitated mycelial growth. In the presence of heat stress, the intracellular IAA content showed a significant increase in the two LeDnaJ07 overexpression strains but only a slight change in the YS55 wild type strain. Moreover, the interaction between LeDnaJ07 and LetrpE was demonstrated via Y2H and BiFC assays. These results suggested that LeDnaJ07 may be involved in regulating IAA biosynthesis and the resistance of L. edodes to heat stresses via interacting with LetrpE.
Introduction
Heat stress is a major constraint in mushroom production. High temperature not only inhibits mycelial growth and fruiting body formation, but also enhances Trichoderma sp. infection and cell membrane fluidity in edible fungi (Lu et al., 2014; Liu et al., 2017; Qiu et al., 2017). Previous studies have reported that Para-aminobenzoic acid (PABA) synthase and nitric oxide reduced ROS (reactive oxygen species) accumulation to alleviate oxidative damage induced by heat stress (Kong et al., 2012a; Lu et al., 2014); catalase, trehalose, HSP and calcium-calmodulin play an important role in regulating the response of the edible fungi to heat stress (Kong et al., 2012b; Deng et al., 2014; Wang et al., 2017; Liu et al., 2018).
Lentinula edodes, one mushroom used for decoctions and essences and alternative medicine, is widely cultivated in the world and ranks second in worldwide production next to Agaricus bisporus (Chang, 2005; Finimundy et al., 2014). During mycelial culture of L. edodes in rotted logs or bags, six Trichoderma species have been isolated and identified in previous studies, and these studies reported that high temperatures caused large losses in L. edodes yield (Cao et al., 2015; Wang G.Z. et al., 2016). Our previous studies found that LeDnaJ07 (named as LeDnaJ in our previous reports) and auxin participated in the response to heat stress in L. edodes (Wang et al., 2018a, b; Zhou et al., 2018).
Heat shock protein 40 (termed DnaJ or J protein), an important member of the heat shock protein family, plays a critical role in modulating the growth and development processes of organism as well as their resistance to abiotic and biotic stresses (Caplan et al., 1992; Suetsugu et al., 2005; Shen and Yu, 2011; Zhou et al., 2012). In plants, the function of DnaJ protein is well-known. DnaJ proteins regulate the resistance of plants to abiotic stresses (heat, cold, salt, and drought) via inducing cell elongation and stabilizing the structure of the photosynthetic system II (Bekhochir et al., 2013; Kong et al., 2014b; Wang et al., 2019). In addition, overexpression of DnaJ protein enhanced the resistance of tobacco to Phytophthora parasitica pv nicotianae and Sclerotinia sclerotiorum via regulating the activity of ascorbic acid peroxidase (APX), Mn-SOD (superoxide) and HSP70 (Rampuria et al., 2018). Moreover, the knockdown of OsDjA6 enhanced the resistance of Oryza sativa to Magnaporthe oryzae (Zhong et al., 2018). For Candida albicans, Ydj1 loss resulted in the failure of morphogenetic switch from yeast to filamentous form (Xie et al., 2017). However, the function of DnaJ protein in macro basidiomycete fungi is less well-known.
Based on our previous studies, the transcript and protein levels of LeDnaJ07 were dramatically upregulated in the heat-resistant strain S606 after heat stress. LeDnaJ07 overexpression in L. edodes strain S606 enhanced the thermotolerance via regulating IAA biosynthesis, while LeDnaJ07 RNAi in L. edodes strain S606 played a negative role in regulating mycelial growth, the resistance to heat stress and T. atroviride and IAA biosynthesis after heat stress (Wang et al., 2018a, b). According to transcriptome and proteome analyses after heat stress, the protein level of LetrpE, a rate-limiting enzyme in the IAA biosynthesis pathway, in the thermotolerance strain S606 was increased by approximately 500-fold after heat stress, while its transcript level was obviously downregulated (Wang et al., 2018a). Further, LetrpE RNAi in S606 played a negative role in regulating L. edodes thermotolerance (Ma et al., 2018).
The objectives of the present study were as follows: (1) to analyze the structure of LeDnaJ07 in L. edodes thermotolerance strain S606 and stress-sensitive strain YS55; (2) to explore the effect of LeDnaJ07 on mycelial growth and resistance to heat stress in YS55; (3) to quantify the IAA content after 24 h of 38°C heat stress in sawdust medium; and (4) to verify the interaction between LeDnaJ07 and LetrpE via Y2H (yeast two-hybrid) and BiFC (bimolecular fluorescence complementation) analyses.
Materials and Methods
Strains and Culture Conditions
L. edodes strain YS55 was used as the recipient host strain for gene overexpression and it was cultured at 25°C on MYG (malt yeast glucose) medium or sawdust medium. E. coli Trans1-T1 and Agrobacterium tumefaciens EHA105 were used for plasmid amplification and infecting L. edodes mycelia, respectively, and they were cultured in 50 μg/ml kanamycin Luria–Bertani (LB) medium.
Extraction of RNA, LeDnaJ07 Cloning and Sequence Analysis
Total RNA was extracted from L. edodes strain S606 and YS55 using the RNAiso Plus (TAKARA, Shanghai, China) method, and isolated RNA was then reverse-transcribed into cDNA using the HiScript II One Step RT-PCR Kit (Vazyme, Nanjing, China) according to the manufacturer’s instruction. Based on L. eodes strain WX-1 genome information1 (Chen et al., 2016), the CDS (coding sequence) of LeDnaJ07 (Le01Gene01273) was amplified by PCR using L. edodes strain S606 and YS55 cDNA (primers listed in Supplementary Table S1), and the fragments were cloned into the pEASY-Blunt vector (TransGen Biotech, Beijing, China) for sequencing. The CDSs containing S606 and YS55 as well as WX-1 were aligned using ClustalW in MEGA 6.0, and the alignment result was visualized by GeneDoc. The protein sequences of LeDnaJ07 were aligned with 22 J proteins in Saccharomyces cerevisiae using the neighbor-joining method in MEGA 6.0.
Vector Construction and Fungal Transformation
The fungal overexpression vector was constructed as previously described (Ding et al., 2011). The Legpd (L. edodes glyceraldehyde-3-phosphate dehydrogenase) promoter was used to induce expression of hygromycin phosphotransferase, and the Leactin promotor was used to induce the mCherry fluorescent protein (mRFP) and LeDnaJ07. The coding sequences of mRFP and LeDnaJ07 were obtained by PCR using primers with the homologous arms containing restriction enzyme sites (EcoRI and KpnI) as well as pBlueScript SK plasmid and L. edodes cDNA as the template (Supplementary Table S1). The overexpression vector and control vector only containing mCherry protein were transferred into the L. edodes strain by A. tumefaciens infection. Nine transformants were selected randomly to analyze the overexpression efficiency of the transformants by qRT-PCR. mRFP expression was assessed by observing fluorescence using a fluorescence microscope, and the stable integration of the target gene into the genome of L. edodes was confirmed by Southern blot analysis (Yin et al., 2015). Two independent overexpression strains with the highest upregulation efficiency and one transformant (control strain) only containing mCherry protein were selected for further study.
Mycelial Growth and Thermotolerance Susceptibility Assays
After 10-day growth at 25°C, the colony diameters of the transgenic and WT strains in the MYG and sawdust medium were measured to evaluate the effect of LeDnaJ07 on L. edodes mycelial growth. Moreover, the LeDnaJ07 over-expressed, control and WT strains were grown in plastic culture bags (15 cm in fold diameter and 30 cm in length) containing 0.8 kg (wet weight) of sterilized sawdust medium (78% hardwood, 20% wheat bran, 1% lime, 1% gypsum and 55% water content). Five mycelial plugs (8 mm in diameter) were inoculated into each culture bag, and 12 culture bags were prepared separately for each of the transformant and wild-type (WT) strains. Culture bags were followed by culture at 25°C in the dark.
To test the effect of LeDnaJ07 overexpression on the resistance of L. edodes against heat stress, thermotolerance assays, involving short- and long- term heat stresses, were performed according to our previous method (Wang et al., 2018b). In the short-term heat stress group, the stress temperature and recovery time were 38°C and 25 d, respectively. Colony diameters and characteristics were used to quantify the sensitivity of the transgenic and WT strains to heat stress, with five replicates for each group.
Detection and Measurement of IAA
L. edodes mycelia treated or untreated by 38°C heat stress for 24 h were collected separately. To analyze IAA differences between transformant and WT strains, mycelial samples were grinded into fine powder in liquid nitrogen. IAA extraction and measurement methods were performed according to our previous study (Wang et al., 2018b).
Yeast Two-Hybrid and Bimolecular Fluorescence Complementation Analyses
The interaction between LeDnaJ07 with LetrpE was verified using the Matchmaker Gold Yeast Two-Hybrid (Y2H) System (Clontech, Palo Alto, CA, United States) (Yin et al., 2015). LeDnaJ07 and LetrpE were introduced into pDEST22 and pDEST32 plasmids as baits and preys, respectively. The bait and prey plasmids were co-transformed into S. cerevisiae strains MaV103 and MaV203 according to the manufacturer’s instructions. Transformed yeast cells were assayed for growth onsynthetic dropout SD/-Trp-Leu-Ura plates, SD/-Trp-Leu-His plates and SD/-Trp-Leu plates containing X-a-galactosidase (X-a-gal) or 3-amino-1,2,4-triazole (3AT) (10 and 25 mM).
The full-length cDNA sequences of LeDnaJ07 and LetrpE were amplified by PCR and cloned into the BamHI/XhoI site of pSYCE-MR and pSCYNE-R vectors, respectively, generating CFPC-LeDnaJ07/LetrpE and LeDnaJ07/LetrpE-CFPN fusion constructs. The constructs were transformed into A. tumefaciens strain AGL-1. Transient expression of proteins in N. benthamiana leaves by A. tumefaciens infiltration was conducted as previously described (Kang et al., 2011; Yang et al., 2018). Cyan fluorescence of fusion proteins was assayed 2–3 d after infiltration using a Zeiss LSM510 with excitation/emission wavelengths of 405 and 477 nm, respectively.
Statistical Analysis
All data averaged from the five independent sample measurements were used to ensure the reliability and reproducibility of the change trend between WT and overexpression strains. The significance of the differences between the analyzed samples was determined by one-way analysis of variance (ANOVA) and tested for significant (P < 0.05) treatment differences using Duncan’s multiple range test.
Results
Analysis of LeDnaJ07 CDS in Different L. edodes Strains
The CDS difference of LeDnaJ07 between heat-resistant strain S606, stress-sensitive strain YS55 and cultivation strain WX-1 was analyzed using the PCR sequecing result. According to the prediction of DnaJ domain in https://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi, J domain located from 10 to 198 bp in LeDnaJ07 CDS (Figure 1A). In terms of sequence alignment, it was found that only four of 1119 base pairs out of J domain exhibited a difference among three L. edodes strains (Figure 1A and Supplementary Figure S1), which made no changes on the amino acid sequence of three LeDnaJ07 proteins. This result indicated that LeDnaJ07 proteins in different L. edodes strains were identical. As shown in Figure 1B, LeDnaJ07 exhibited a 92% similarity to SIS1 in S. cerevisiae, indicating that LeDnaJ07 could play an important role during translation initiation.
Figure 1. LeDnaJ07 sequence analysis. (A) Structure analysis and sequence alignment of LeDnaJ07 CDS in three L. edodes strains. (B) Molecular phylogenetic tree of LeDnaJ07 generated with the neighbor-joining (NJ) method using MEGA 7.0. An unrooted phylogenetic tree was generated based on the alignment of the amino acid (AA) sequences containing LeDnaJ07 and 22 S. cerevisiae J proteins.
Construction of LeDnaJ07 Overexpression Strains
The overexpression vector pCAMBIA1300-g-mo was used to express the fusion protein mRFP-LeDnaJ07, and the hygromycin B resistance gene in that overexpression vector was treated as the selectable marker (Figure 2A). Nevertheless, the vector pCAMBIA1300-g-m only expressing the mRFP was treated the contorl vector. After introducing the expression vector and the control vector into the mycelia of L. edodes via A. tumefaciens mediation, the expression level of LeDnaJ07 was used to confrim the transformants. Among all the transformants, two overexpression transformants LeDnaJ07-mo-1 and LeDnaJ07-mo-9 had an about two and four-fold upregulation (P < 0.05), respectively, but no significant expression changes found in other transformatns and two control transformants Le-m-1 and Le-m-2 (Figure 2B). Southern blot showed that one copy of the insert fragment was found in overexpression strains LeDnaJ07-mo-1 and LeDnaJ07-mo-9, but no copy in the WT strain (Figure 2C), indicating the integration of the insert fragment including in LeDnaJ07 gene into L. edodes genome. To verify the expression level of the introduced mCherry reporter gene, mycelia fluorescence of three individual transformants grown on MYG medium were detected using a fluorescence microscope. As shown in Figure 3, the clear distribution of red fluorescence was found in the mycelia of three individual transformants. These results suggested that the LeDnaJ07 overexpression recombinants were successfully obtained.
Figure 2. Vector map and identification of LeDnaJ07 overexpression transformants. (A) Vector map of LeDnaJ07 overexpression. (B) qRT-PCR analysis of LeDnaJ07 overexpression transformants. YS55, wild type strain; Le-m-1/2, Control transgenic strains; LeDnaJ07-mo-1-9, LeDnaJ07 overexpression strains; *, represents the significant difference. (C) Southern blot analysis of genomic DNA isolated from the transformants and WT strain digested with HindIII. Lane 1-5, Maker, pCAMBIA1300-g plasmid, LeDnaJ07-mo-1, LeDnaJ07-mo-9, and the WT strain YS55, respectively.
Figure 3. Expression of mCherry in the LeDnaJ07 overexpression transformant, control transgenic and WT strains. (A–D) Detection of L. edodes mycelia without fluorescence. (E–H) Detection of L. edodes mycelia with fluorescence under red light. Bar, 10 μm.
Overexpression of LeDnaJ07 Enhances the Mycelial Growth of L. edodes
As shown in Figure 4, in MYG medium, the colony diameters of the two overexpression transformants (LeDnaJ07-mo-1 and LeDnaJ07-mo-9) were 7.28 and 6.93 cm after 9 days of inoculation, with 5.57 and 5.20 cm diameters for the control and WT strains (Figures 4A,B); and the colony diameters of the two overexpression transformants were 7.03 and 6.45 cm after inoculation for 15 days in sawdust medium, with diameters of 5.80 and 5.55 cm for the control and WT strain (Figures 4C,D). Besides, it was documented that the mycelia of LeDnaJ07 over-expressed transformants were full of the cultivation bags after 45 days of growth, while the mycelia of WT strain YS55 and control strain Le-m-1 covered 70% of the cultivation bags (not shown), indicating that improving the expression of LeDnaJ07 could promote the growth of L. edodes mycelia in MYG and sawdust medium.
Figure 4. Effect of LeDnaJ07 overexpression on the growth of L. edodes mycelia. (A) and (B) Colony characteristics and diameters of the LeDnaJ07 overexpression transformant, control transgenic and the WT strains in MYG medium after 9 days of inoculation. (C) and (D) Colony characteristics and diameters of the LeDnaJ07 overexpression transformant, control transgenic and WT strains in sawdust medium after 15 days of inoculation. Each bar represents mean ± standard deviation (SD) (n = 5). *, The colony diameters of the LeDnaJ07 overexpression transformants were significantly different from those of the WT and control transgenic strains (P < 0.05).
LeDnaJ07 Overexpression Is of Benefit to L. edodes Thermotolerance
The effect of LeDnaJ07 on L. edodes thermotolerance was estimated by comparing the colony diameters after heat stress among WT, control and LeDnaJ07 overexpression transformant strains. Long-term heat stress lasted for 15 days at 31°C, and short-term heat stress lasted 24 h at 38°C. From the perspective of the thermotolerance assays, no growth was observed in the mycelia of all strains after 31°C heat stress for 15 days. Nevertheless, after 15 days of recovery at 25°C, only the mycelia of the two LeDnaJ07 overexpressed transformants with a colony diameter about 3 cm regrew at 31°C heat stress, whereas an about 2 cm colony diameter was found in WT and control transgenic strains (Figure 5A). After 24 h of heat stress at 38°C, the mycelia of the two overexpression transformants showed a colony diameter about 4.5 cm after a 25-day recovery at 25°C, but the mycelia of control transgenic and WT strains showed a colony diameter of 2.0 cm and were dead and dissolved (Figure 5B). The similar results of the long-term and short-term heat stress assays demonstrated that LeDnaJ07 promoted the recovery capacity and thermotolerance of L. edodes mycelia in response to heat stress.
Figure 5. LeDnaJ07 overexpression enhances L. edodes thermotolerance and IAA biosynthesis after heat stress. (A) Colony diameters of the WT, control transgenic and LeDnaJ07 overexpression transformant strains grown in sawdust medium for 15 days of recovery from the 15 days of 31°C heat stress. (B) Colony diameters of the WT, control transgenic and LeDnaJ07 overexpression transformant strains in sawdust medium after 25 days of recovery from the 24 h of 38°C heat stress. (C) IAA concentration change in the wild type YS55 and LeDnaJ07 overexpression transformants after 38°C heat stress for 24 h. Each bar represents mean ± standard deviation (SD) (n = 5). NH, not heat stress. HS, heat stress. *, significant difference (P < 0.05).
The Overexpression of LeDnaJ07 Promotes Intracellular IAA Biosynthesis After Heat Stresses
At 25°C, the intracellular IAA concentrations of YS55, Le-m-1 and the two LeDnaJ07 overexpression strains displayed a slight difference, but they showed significant differences after heat stress (Figure 5C). After 24 h of heat stress at 38°C, the intracellular IAA concentration had a 7.16 and 8.12-fold increase in the two LeDnaJ07 overexpression transformants, but only a 1.26 and 1.17-fold increase in the WT strain YS55 and control transgenic strain Le-m-1, indicating that LeDnaJ07 was beneficial to IAA biosynthesis during the response to heat stress.
Interaction Between LeDnaJ07and LetrpE in Yeast and Tobacco Leaf Cells
According to the result of self-activation assay, it was found that the yeast cells only containg one of LeDnaJ07 and LetrpE could grow ont SD/-Trp plates, but no growth found on SD/-Trp-Leu and SD/-Trp-Ade plates, suggesting that they showed no self-activation effect in transgenic yeast cells (Supplementary Figure S2). In the Y2H assay, after 3 days of culture at 30°C, yeasts from all mixtures grew on SD/-Trp-Leu plates (Figure 6). The yeasts from mixture containing the positive control (pEXP32-Krev1 + pEXP22-RalGDS wt) turned blue, and the yeasts from the weak positive interaction control (pEXP32-Krev1 + pEXP22-RalGDS m1) and the tested group (PDEST22-LeDnaJ07 + PDEST32-LetrpE and PDEST22-LetrpE + PDEST32-LeDnaJ07) exhibited light blue. Whereas, the yeasts from the negative control (pEXP32-Krev1 + pEXP22-RalGDS m2) displayed white. In addition, the mated yeasts from the positive control and tested groups exhibited the growth on SD/-Trp-Leu-Ura plates (Figure 6). Except for the negative control, the mated yeasts of other four groups grew on SD/-Leu-Trp plates with 10 and 25 mM 3AT (Figure 7). The above results indicated that a weak interaction occurred between LeDnaJ07 and LetrpE. Furthermore, as shown in Figure 8, the BiFC assay showed that cells from the positive control (p1300-SPYCE(MR)-Krev1 + p1300-SPYNE(R)-RalGDS wt) and tested groups (p1300-SPYCE(MR)-LeTrpE + p1300-SPYNE(R)-LeDnaJ07 and p1300-SPYNE(R)-LetrpE + p1300-SPYCE(MR)-LeDnaJ07) exhibited green fluorescence, but no green fluorescence was observed in the negative group (p1300-SPYCE(MR)-Krev1 + p1300-SPYNE(R)-RalGDS m2). Taken together, these data verified that LeDnaJ07 had an interaction with LetrpE.
Figure 6. Interaction verification of LeDnaJ07 with LetrpE in the Y2H system on the plates with SD/-Leu-Trp and SD/-Leu-Trp-Ura. Tested groups, DEST22-LeDnaJ07 + PDEST32-LetrpE, and PDEST22-LetrpE + PDEST32-LeDnaJ07; Positive control, pEXP32-Krev1 + pEXP22-RalGDS wt; Weak position interaction control, pEXP32-Krev1 + pEXP22-RalGDS m1; Negative control, pEXP32-Krev1 + pEXP22-RalGDS m2.
Figure 7. Interaction verification of LeDnaJ07 with LetrpE in the Y2H system on the plates with SD/-Leu-Trp-His and SD/-Leu-Trp and different concentration 3AT. Tested groups, DEST22-LeDnaJ07 + PDEST32-LetrpE and PDEST22-LetrpE + PDEST32-LeDnaJ07; Positive control, pEXP32-Krev1 + pEXP22-RalGDS wt; Weak position interaction control, pEXP32-Krev1 + pEXP22-RalGDS m1; Negative control, pEXP32-Krev1 + pEXP22-RalGDS m2.
Figure 8. Interaction of LetrpE with LeDnaJ07 in plant cells. Tested groups, p1300-SPYCE(MR)-LetrpE + p1300-SPYNE(R)-LeDnaJ07 and p1300-SPYCE(MR)-LeDnaJ07 + p1300-SPYNE(R)-LetrpE, Positive control, p1300-SPYCE(MR)-Krev1 + p1300-SPYNE(R)-RalGDS wt; Negative control, p1300-SPYCE(MR)-Krev1 + p1300-SPYNE(R)-RalGDS m2(negative control). Bar, 10 μm.
Discussion
Numerous studies have shown that DnaJ proteins are involved in biotic and abiotic stresses for human and plants (Shen and Yu, 2011; Kakkar et al., 2012; Lee et al., 2018; Zhong et al., 2018). However, the regulation of the DnaJs on the resistance of higher basidiomycetes to biotic and abiotic stresses remains poorly understood. According to our previous studies, it was documented that the RNAi of the LeDnaJ07 decreased mycelial growth and the resistance to heat stress, while LeDnaJ07 overexpression enhanced the thermotolerance of L. edodes heat-resistant strain S606 (Wang G.Z. et al., 2016, Wang et al., 2018b). However, it is worthy of study whether LeDnaJ07 overexpression regulates the resistance of other L. edodes strains to stresses or not, how LeDnaJ07 regulates the response of L. edodes to thermotolerance. In this study, we intended to provide evidence that J domain in different L. edodes strains was consistent, and the overexpression of the chaperone LeDnaJ07 participated in regulating thermotolerance and mycelial growth by targeting LetrpE in the stress-sensitive strain YS55.
In plant, a large number of papers reported that DnaJ proteins regulated growth and development. For Arabidopsis thaliana and rice, DnaJ protein loss led to an obvious late-flowering trait and largely abnormal cellular structures (Shen and Yu, 2011; Zhu et al., 2015). Overexpression of BIL2, one gene encoding the mitochondrial DnaJ protein, promoted elongation of A. thaliana cells by promoting ATP synthesis (Bekhochir et al., 2013). Silencing of PSA2, which encodes DnaJ family proteins, led to an obvious decrease in chlorophylls and total carotenoids, further variegated leaves and retarded growth (Wang Y.W. et al., 2016). The present study documented that colony diameters of two overexpression transformants were significantly larger than them of the control transgenic and WT strains on sawdust and MYG medium at the same culture condition (Figure 4), indicating that LeDnaJ07 overexpression exhibited a positive role in regulating L. edodes mycelial growth and development. These results were consistent with the results of our previous study that LeDnaJ07 silence resulted in a dramatically retarded mycelial growth in the heat-resistant strain S606 (Wang et al., 2018b). Nevertheless, it is still unknown how LeDnaJ07 overexpression promotes mycelial growth.
Furthermore, an increasing number of reports have demonstrated that the high expression and accumulation of DnaJ proteins positively regulated the thermotolerance of plants. For example, the double knock-out of AtDjA2 and AtDjA3 impaired the thermotolerance of A. thaliana young seedlings, whereas overexpression of both genes increased the thermotolerance of transgenic plants (Li et al., 2007). In transgenic tomatoes, DnaJ protein overexpression facilitated heat tolerance by regulating ROS and H2O2 and protected Rubisco activity from degradation under heat stress by keeping the levels of proteolytic enzymes low (Kong et al., 2014a; Wang et al., 2015, 2019). In the present study, the mycelia of the two LeDnaJ07 overexpression strains regrew after 15-day of heat stress at 31°C and 24 h of heat stress at 38°C, but no growth was observed in the control transgenic and WT strains at these conditions (Figures 5A,B). In addition, we observed that mycelia of the control transgenic and WT strains were dissolved after 38°C heat stress, whereas the overexpression strains were mildly affected by heat stress. This difference in the phenotype trait of the test L. edodes strains in response to heat stress demonstrated that the LeDnaJ07 overexpression alleviated heat stress, providing further evidence that DnaJ proteins can enhance the thermotolerance in different L. edodes strains.
The present study also showed that overexpression of LeDnaJ07 in stress-sensitive strain YS55 promoted the IAA biosynthesis under heat stress (Figure 5C), which is consistent with our previous studies. LeDnaJ07 RNAi and overexpression decreased and promoted, respectively, the intracellular IAA concentration after heat stress, and 0.01 mM IAA partly restored the resistance of LeDnaJ07 RNAi strains to heat stresses (Wang G.Z. et al., 2016, Wang et al., 2018b), indicating that LeDnaJ07 is quite important for IAA biosynthesis under heat stress condition. Anthranilate synthase TrpE is a key rate-limiting enzyme in the tryptophan-dependent IAA biosynthesis pathway (Ishimoto et al., 2010). In our study, the yeast two-hybrid system and BiFC assays proved that LeDnaJ07 interacts with L. edoeds LetrpE (Figures 6–8), suggesting that the LeDnaJ07/LetrpE machinery possibly may play a significant role in thermotolerance by regulating IAA biosynthesis. According to our previous study, exogenous IAA and its analoges may alleviate the effect of oxidative damage induced by heat stress on the mycelia of L. edodes by regulating the expression of redox enzymes, such as SOD and LOX (Zhou et al., 2018). These results demonstrated that LeDnaJ07 overexpression enhanced the extracellular IAA content by interacting with LetrpE (a rate-limiting enzyme in the IAA biosynthesis pathway), and then improved the thermotolerance of L. edodes mycelia by mediating redox enzymes.
Conclusion
In summary, we cloned and analyzed the LeDnaJ07 gene in L. edodes heat-resistant strain S606 and stress-sensitive strain YS55. Overexpression of LeDnaJ07 in YS55 enhanced the tolerance to heat stress in the transgenic strains, with an obvious increase in mycelial growth and intracellular IAA concentration in the transgenic strains compared with the control transgenic and WT strains. In addition, the present study for the first time showed that LeDnaJ07 interacted with LetrpE. We constructed a model for the role of LeDnaJ07 and the IAA signal pathway in enhancing L. edodes thermotolerance (Figure 9). This study provides valuable information for the relative expression level of DnaJ proteins in stress-resistant mushroom breeding. Further study will focus on the mechanism by which LeDnaJ07 regulates L. edodes thermotolerance via the IAA signal pathway.
Figure 9. Schematic model for the role of IAA and LeDnaJ07 in enhancing thermotolerance of L. edodes.
Data Availability Statement
All datasets generated for this study are included in the article/Supplementary Material.
Author Contributions
GW, YZ, HK, YX, YB, and YG conceptualized the study. CW helped with the data curation. GW, YL, and YG contributed to the formal analysis. YB was responsible for the funding acquisition. YL and CW carried out the investigation. GW, YL, CM, HK, and YG worked on the methodology. YX contributed to the resources. GW, YL, and CW were responsible for the validation. GW, YL, and CM helped with the visualization. GW wrote the original draft. YZ, YB, and YG reviewed and edited the manuscript.
Funding
This research was funded by the National Natural Science Foundation of China (Grant Nos. 31672211 and 31972476).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2020.00707/full#supplementary-material
Footnotes
References
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Keywords: DnaJ protein, Lentinula edodes, thermotolerance, IAA, yeast two-hybrid, BiFC, LetrpE
Citation: Wang G, Luo Y, Wang C, Zhou Y, Mou C, Kang H, Xiao Y, Bian Y and Gong YH (2020) Hsp40 Protein LeDnaJ07 Enhances the Thermotolerance of Lentinula edodes and Regulates IAA Biosynthesis by Interacting LetrpE. Front. Microbiol. 11:707. doi: 10.3389/fmicb.2020.00707
Received: 24 December 2019; Accepted: 26 March 2020;
Published: 17 April 2020.
Edited by:
Baokai Cui, Beijing Forestry University, ChinaReviewed by:
Dapeng Bao, Institute of Edible Fungi (SAAS), ChinaGerardo Díaz-Godínez, Autonomous University of Tlaxcala, Mexico
Copyright © 2020 Wang, Luo, Wang, Zhou, Mou, Kang, Xiao, Bian and Gong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yu Hua Gong, Z29uZ3l1aHVhQG1haWwuaHphdS5lZHUuY24=
†These authors have contributed equally to this work