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Background: Calcium ions (Ca2+), secondary messengers, are crucial for the signal transduction process of the interaction between plants and pathogens. Ca2+ signaling also regulates autophagy. As plant calcium signal-decoding proteins, calcium-dependent protein kinases (CDPKs) have been found to be involved in biotic and abiotic stress responses. However, information on their functions in response to powdery mildew attack in wheat crops is limited. Result: In the present study, the expression levels of TaCDPK27, four essential autophagy-related genes (ATGs) (TaATG5, TaATG7, TaATG8, and TaATG10), and two major metacaspase genes, namely, TaMCA1 and TaMCA9, were increased by powdery mildew (Blumeria graminis f. sp. tritici, Bgt) infection in wheat seedling leaves. Silencing TaCDPK27 improves wheat seedling resistance to powdery mildew, with fewer Bgt hyphae occurring on TaCDPK27-silenced wheat seedling leaves than on normal seedlings. In wheat seedling leaves under powdery mildew infection, silencing TaCDPK27 induced excess contents of reactive oxygen species (ROS); decreased the activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT); and led to an increase in programmed cell death (PCD). Silencing TaCDPK27 also inhibited autophagy in wheat seedling leaves, and silencing TaATG7 also enhanced wheat seedling resistance to powdery mildew infection. TaCDPK27-mCherry and GFP-TaATG8h colocalized in wheat protoplasts. Overexpressed TaCDPK27-mCherry fusions required enhanced autophagy activity in wheat protoplast under carbon starvation. Conclusion: These results suggested that TaCDPK27 negatively regulates wheat resistance to PW infection, and functionally links with autophagy in wheat. [ABSTRACT FROM AUTHOR]

As essential calcium ion (Ca2+) sensors in plants, calcium-dependent protein kinases (CDPKs) function in regulating the environmental adaptation of plants. However, the response mechanism of CDPKs to salt stress is not well understood. In the current study, the wheat salt-responsive gene TaCDPK27 was identified. The open reading frame (ORF) of TaCDPK27 was 1875 bp, coding 624 amino acids. The predicted molecular weight and isoelectric point were 68.905 kDa and 5.6, respectively. TaCDPK27 has the closest relationship with subgroup III members of the CDPK family of rice. Increased expression of TaCDPK27 in wheat seedling roots and leaves was triggered by 150 mM NaCl treatment. TaCDPK27 was mainly located in the cytoplasm. After NaCl treatment, some of this protein was transferred to the membrane. The inhibitory effect of TaCDPK27 silencing on the growth of wheat seedlings was slight. After exposure to 150 mM NaCl for 6 days, the NaCl stress tolerance of TaCDPK27-silenced wheat seedlings was reduced, with shorter lengths of both roots and leaves compared with those of the control seedlings. Moreover, silencing of TaCDPK27 further promoted the generation of reactive oxygen species (ROS); reduced the activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT); aggravated the injury to photosystem II (PS II); and increased programmed cell death (PCD) in wheat leaves under NaCl treatment, confirming that the TaCDPK27-silenced seedlings exhibited more NaCl injury than control seedlings. Taken together, the decrease in NaCl tolerance in TaCDPK27-silenced seedlings was due to excessive ROS accumulation and subsequent aggravation of the NaCl-induced PCD. TaCDPK27 may be essential for positively regulating salt tolerance in wheat seedlings. [ABSTRACT FROM AUTHOR]

Context: Salt stress harms plant growth and limits crop productivity. Autophagy is a material decomposition and metabolism pathway that is central to regulating plant responses to environmental stimuli and may be employed in plant breeding for stress tolerance. The autophagy-related gene ATG8 has become an essential tool for monitoring autophagic activity. Aims: We aimed to determine the effects of increased autophagic activity via overexpression of ATG8 on tolerance of wheat (Triticum aestivum L.) seedlings to NaCl stress. Methods: Salt-tolerant wheat cv. Jimai22 was used to produce TaATG8a -overexpressing wheat seedlings using Foxtail mosaic virus based virus-mediated overexpression technology. TaATG8a -overexpressing seedlings were exposed to NaCl stress for 6 days. Key results: Overexpression of TaATG8a enhanced autophagic activity and improved salt stress tolerance of wheat seedlings. Overexpression of TaATG8a also reduced damage to photosystem II, reduced excess accumulation of reactive oxygen species, increased the activities of superoxide dismutase, peroxidase and catalase, and suppressed programmed cell death in wheat seedling leaves during NaCl treatment. Conclusions: Overexpression of TaATG8a conferred higher tolerance of wheat seedlings to NaCl stress and suppressed salt-induced programmed cell death, accompanied by increased autophagic activity. Implications: This study provides genetic resources and a theoretical basis for stress tolerance breeding in wheat. The present study examined whether overexpression of TaATG8 enhanced tolerance of wheat seedlings to NaCl stress. TaATG8 -overexpressed seedlings showed higher autophagic activity, decreased ROS production, and improved activities of POD, SOD, and CAT under NaCl stress. TaATG8 -mediated autophagy inhibited programmed cell death in wheat leaves at the seedling stage during NaCl treatment. [ABSTRACT FROM AUTHOR]