Identification of as a target of ATHB2 and TCP13 during shade response.

Front Plant Sci

Department of Biological Science and Institute of Women's Health, Sookmyung Women's University, Seoul, Republic of Korea.

Published: April 2023

The shade avoidance syndrome (SAS) is a collective adaptive response of plants under shade highlighted by characteristic phenotypes such as hypocotyl elongation, which is largely mediated by concerted actions of auxin and GA. We identified ATHB2, a homeodomain-leucine zipper (HD-Zip) domain transcription factor known to be rapidly induced under shade condition, as a positive regulator of GA biosynthesis necessary for the SAS by transactivating the expression of , a key gene in the GA biosynthesis pathway. Based on promoter deletion analysis, EMSA and ChIP assay, ATHB2 appears to regulate the expression as a direct binding target. We also found that the expression is under negative control by TCP13, the effect of which can be suppressed by presence of ATHB2. Considering a rapid induction kinetics of , this relationship between ATHB2 and TCP13 may allow ATHB2 to play a shade-specific activator for by derepressing a pre-existing activity of TCP13.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160606PMC
http://dx.doi.org/10.3389/fpls.2023.1158288DOI Listing

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Identification of as a target of ATHB2 and TCP13 during shade response.

Front Plant Sci

April 2023

Department of Biological Science and Institute of Women's Health, Sookmyung Women's University, Seoul, Republic of Korea.

The shade avoidance syndrome (SAS) is a collective adaptive response of plants under shade highlighted by characteristic phenotypes such as hypocotyl elongation, which is largely mediated by concerted actions of auxin and GA. We identified ATHB2, a homeodomain-leucine zipper (HD-Zip) domain transcription factor known to be rapidly induced under shade condition, as a positive regulator of GA biosynthesis necessary for the SAS by transactivating the expression of , a key gene in the GA biosynthesis pathway. Based on promoter deletion analysis, EMSA and ChIP assay, ATHB2 appears to regulate the expression as a direct binding target.

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