Antagonistic Regulation of ABA Responses by Duplicated Tandemly Repeated DUF538 Protein Genes in Arabidopsis

Yingying Li; Wei Wang; Na Zhang; Yuxin Cheng; Saddam Hussain; Yating Wang; Hainan Tian; Hadia Hussain; Rao Lin; Yuan Yuan; Chen Wang; Tianya Wang; Shucai Wang

doi:10.3390/plants12162989

Antagonistic Regulation of ABA Responses by Duplicated Tandemly Repeated DUF538 Protein Genes in Arabidopsis

Plants (Basel). 2023 Aug 19;12(16):2989. doi: 10.3390/plants12162989.

Authors

Yingying Li¹, Wei Wang², Na Zhang¹, Yuxin Cheng¹, Saddam Hussain², Yating Wang¹, Hainan Tian¹, Hadia Hussain¹, Rao Lin¹, Yuan Yuan¹, Chen Wang¹, Tianya Wang¹, Shucai Wang^{1

2}

Affiliations

¹ Key Laboratory of Molecular Epigenetics of MOE, Northeast Normal University, Changchun 130024, China.
² Laboratory of Plant Molecular Genetics & Crop Gene Editing, School of Life Sciences, Linyi University, Linyi 276000, China.

Abstract

The plant hormone ABA (abscisic acid) regulates plant responses to abiotic stresses by regulating the expression of ABA response genes. However, the functions of a large portion of ABA response genes have remained unclear. We report in this study the identification of ASDs (ABA-inducible signal peptide-containing DUF538 proteins), a subgroup of DUF538 proteins with a signal peptide, as the regulators of plant responses to ABA in Arabidopsis. ASDs are encoded by four closely related DUF538 genes, with ASD1/ASD2 and ASD3/ASD4 being two pairs of duplicated tandemly repeated genes. The quantitative RT-PCR (qRT-PCR) results showed that the expression levels of ASDs increased significantly in response to ABA as well as NaCl and mannitol treatments, with the exception that the expression level of ASD2 remained largely unchanged in response to NaCl treatment. The results of Arabidopsis protoplast transient transfection assays showed that ASDs were localized on the plasma membrane and in the cytosol and nucleus. When recruited to the promoter of the reporter gene via a fused GD domain, ASDs were able to slightly repress the expression of the co-transfected reporter gene. Seed germination and cotyledon greening assays showed that ABA sensitivity was increased in the transgenic plants that were over-expressing ASD1 or ASD3 but decreased in the transgenic plants that were over-expressing ASD2 or ASD4. On the other hand, ABA sensitivity was increased in the CRISPR/Cas9 gene-edited asd2 single mutants but decreased in the asd3 single mutants. A transcriptome analysis showed that differentially expressed genes in the 35S:ASD2 transgenic plant seedlings were enriched in several different processes, including in plant growth and development, the secondary metabolism, and plant hormone signaling. In summary, our results show that ASDs are ABA response genes and that ASDs are involved in the regulation of plant responses to ABA in Arabidopsis; however, ASD1/ASD3 and ASD2/ASD4 have opposite functions.

Keywords: ABA; ASDs; Arabidopsis; CRISPR/Cas9; DUF538 proteins.

Abstract

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