An AP2/ERF member LlERF012 confers thermotolerance via activation of HSF pathway in lily.

Plant Cell Environ

Key Laboratory of Landscaping Agriculture, Ministry of Agriculture and Rural Affairs/Key Laboratory of Biology of Ornamental Plants in East China, National Forestry and Grassland Administration, College of Horticulture, Nanjing Agricultural University, Nanjing, China.

Published: December 2024

AI Article Synopsis

  • Heat stress transcription factors (HSFs) play a critical role in how plants react to heat stress, although their regulatory networks, particularly those involving HSFBs, are not fully understood.
  • This study focused on the interaction between LlERF012 and LlHSFA1 in lilies, showing that LlERF012 positively regulates thermotolerance by activating LlHSFB1 and enhancing its transactivation and DNA-binding capabilities.
  • The research found that overexpressing LlERF012 improves heat tolerance in transgenic Arabidopsis and lilies, while silencing it decreases thermotolerance, indicating that the LlERF012-LlHSFA1 interaction is essential for coordinating the functions of different HSFs in response to heat stress

Article Abstract

Heat stress transcription factors (HSFs) are core factors of plants in response to heat stress (HS), but their regulatory network is complicated and remains elusive in a large part, especially HSFBs. In this study, we reported that the LlERF012-LlHSFA1 module participates in heat stress response (HSR) by directly regulating HSF pathway in lily (Lilium longiflorum). LlHSFB1 was confirmed as a positive regulator in lily thermotolerance and a heat-inducible AP2/ERF member LlERF012 (Ethylene Response Factor 012) was further identified to be a direct trans-activator of LlHSFB1. Overexpression of LlERF012 elevated the thermotolerance of transgenic Arabidopsis and lily, but silencing LlERF012 reduced thermotolerance in lily. Further analysis showed LlERF012 interacted with LlHSFA1, which led to enhanced transactivation activity and DNA-binding capability of LlERF012. In addition, LlERF012 also directly activated the expression of LlHSFA1 by binding its promoter. As expected, we found that LlERF012 bound the promoters of LlHSFA2, LlHSFA3A, and LlHSFA3B to stimulate their expression, and LlERF012-LlHSFA1 interaction enhanced these activation effects. Overall, our data suggested that LlERF012 was a key factor for lily thermotolerance and the LlERF012-LlHSFA1 interaction synergistically regulated the activity of the HSF pathway including the class A and B members, which might be of great significance for coordinating the functions of different HSFs.

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Source
http://dx.doi.org/10.1111/pce.15058DOI Listing

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