4.7 Article

AtERF71/HRE2, an Arabidopsis AP2/ERF Transcription Factor Gene, Contains Both Positive and Negative Cis-Regulatory Elements in Its Promoter Region Involved in Hypoxia and Salt Stress Responses

Journal

Publisher

MDPI
DOI: 10.3390/ijms23105310

Keywords

Arabidopsis; cis-regulatory element; ERF-VII; HAT22; ABIG1; HD-Zip II; HRE2; hypoxia; salt stress

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Education [2020R1I1A3065749, 2020R1I1A1A01065816]
  2. National Research Foundation of Korea [2020R1I1A1A01065816, 2020R1I1A3065749] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this study, the researchers identified the hypoxia- and salt stress-responsive region(s) in the HRE2 promoter. They found that the -116 to -2 region is responsible for both hypoxia and salt stress responses. They also discovered that HAT22/ABIG1, a member of the HD-Zip II subfamily, binds to this region and negatively regulates the transcription of HRE2.
In the signal transduction network, from the perception of stress signals to stress-responsive gene expression, various transcription factors and cis-regulatory elements in stress-responsive promoters coordinate plant adaptation to abiotic stresses. Among the AP2/ERF transcription factor family, group VII ERF (ERF-VII) genes, such as RAP2.12, RAP2.2, RAP2.3, AtERF73/HRE1, and AtERF71/HRE2, are known to be involved in the response to hypoxia in Arabidopsis. Notably, HRE2 has been reported to be involved in responses to hypoxia and osmotic stress. In this study, we dissected HRE2 promoter to identify hypoxia- and salt stress-responsive region(s). The analysis of the promoter deletion series of HRE2 using firefly luciferase and GUS as reporter genes indicated that the -116 to -2 region is responsible for both hypoxia and salt stress responses. Using yeast one-hybrid screening, we isolated HAT22/ABIG1, a member of the HD-Zip II subfamily, which binds to the -116 to -2 region of HRE2 promoter. Interestingly, HAT22/ABIG1 repressed the transcription of HRE2 via the EAR motif located in the N-terminal region of HAT22/ABIG1. HAT22/ABIG1 bound to the 5 '-AATGATA-3 ' sequence, HD-Zip II-binding-like cis-regulatory element, in the -116 to -2 region of HRE2 promoter. Our findings demonstrate that the -116 to -2 region of HRE2 promoter contains both positive and negative cis-regulatory elements, which may regulate the expression of HRE2 in responses to hypoxia and salt stress and that HAT22/ABIG1 negatively regulates HRE2 transcription by binding to the HD-Zip II-binding-like element in the promoter region.

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