Hussain Hadia, Cheng Yuxin, Wang Yating, Yuan Yuan, Li Yingying, Tian Hainan, Hussain Saddam, Chen Siyu, Lin Rao, Wang Tianya, Wang Shucai
Key Laboratory of Molecular Epigenetics of MOE, Northeast Normal University, Changchun 130024, China.
Laboratory of Plant Molecular Genetics & Crop Gene Editing, School of Life Sciences, Linyi University, Linyi 276000, China.
Plants (Basel). 2023 Feb 14;12(4):852. doi: 10.3390/plants12040852.
The plant hormone abscisic acid (ABA) is able to regulate the expression of ABA-responsive genes via signaling transduction, and thus plays an important role in regulating plant responses to abiotic stresses. Hence, characterization of unknown ABA response genes may enable us to identify novel regulators of ABA and abiotic stress responses. By using RT-PCR analysis, we found that the expression levels of ()and , two closely related unknown function genes, were increased in response to ABA treatment. Amino acid sequence analyses show that ASR1 contains an L×L×L motif and both ASR1 and ASR2 are enriched in serine. Transfection assays in Arabidopsis leaf protoplasts show that ASR1 and ASR2 were predominantly localized in the nucleus and were able to repress the expression of the reporter gene. The roles of ASRs in regulating ABA responses were examined by generating transgenic Arabidopsis plants over-expressing and respectively, and CRISPR/Cas9 gene-edited single and double mutants for and . In both the seed germination and cotyledon greening assays, ABA sensitivity remained largely unchanged in the over-expression transgenic plants and the single mutants of and , but greatly increased ABA sensitivity was observed in the double mutants. In root elongation assays, however, decreased ABA sensitivity was observed in the : and : transgenic plants, whereas increased ABA sensitivity was observed in the and single mutants, and ABA sensitivity was further increased in the double mutants. Transcriptome analysis show that the differentially expressed genes (DEGs) down-regulated in the : transgenic plant seedlings, but up-regulated in the double mutant seedlings were highly enriched in processes including responses to plant hormones and stress stimuli. Taken together, our results show that and are closely related ABA response genes, ASR1 and ASR2 are serine-rich novel transcription repressors, and they negatively regulate ABA responses in Arabidopsis in a redundant manner.
植物激素脱落酸(ABA)能够通过信号转导调节ABA响应基因的表达,因此在调节植物对非生物胁迫的响应中发挥重要作用。因此,鉴定未知的ABA响应基因可能使我们能够识别ABA和非生物胁迫响应的新型调节因子。通过逆转录聚合酶链反应(RT-PCR)分析,我们发现两个密切相关的未知功能基因()和的表达水平在ABA处理后升高。氨基酸序列分析表明,ASR1含有一个L×L×L基序,并且ASR1和ASR2都富含丝氨酸。在拟南芥叶原生质体中的转染试验表明,ASR1和ASR2主要定位于细胞核中,并且能够抑制报告基因的表达。通过分别产生过表达和的转基因拟南芥植物,以及针对和的CRISPR/Cas9基因编辑的单突变体和双突变体,研究了ASRs在调节ABA响应中的作用。在种子萌发和子叶绿化试验中,过表达转基因植物以及和的单突变体中的ABA敏感性基本保持不变,但在双突变体中观察到ABA敏感性大大增加。然而,在根伸长试验中,在:和:转基因植物中观察到ABA敏感性降低,而在和单突变体中观察到ABA敏感性增加,并且在双突变体中ABA敏感性进一步增加。转录组分析表明,在:转基因植物幼苗中下调但在双突变体幼苗中上调的差异表达基因(DEGs)在包括对植物激素和胁迫刺激的响应等过程中高度富集。综上所述,我们的结果表明和是密切相关的ABA响应基因,ASR1和ASR2是富含丝氨酸的新型转录抑制因子,它们以冗余方式负调节拟南芥中的ABA响应。