Nakano Yoshimi, Kawai Maki, Arai Moeca, Fujiwara Sumire
Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8566, Japan.
Graduate School of Science and Technology, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan.
Plant Biotechnol (Tokyo). 2023 Dec 25;40(4):337-344. doi: 10.5511/plantbiotechnology.23.0920a.
Correct flower organ formation at the right timing is one of the most important strategies for plants to achieve reproductive success. Ectopic overexpression of LATE FLOWERING (LATE) is known to induce late flowering, partly through suppressing expression of the florigen-encoding gene () in . LATE is one of the C2H2 zinc finger transcription factors, and it has a canonical transcriptional repression domain called the ethylene-responsive element-binding factor-associated amphiphilic repression (EAR) motif at the end of its C terminus. Therefore, LATE is considered a transcriptional repressor, but its molecular function remains unclear. Our genome-edited mutants exhibited no distinct phenotype, even in flowering, indicating the presence of redundancy from other factors. To reveal the molecular function of LATE and factors working with it, we investigated its transcriptional activity and interactions with other proteins. Transactivation activity assay showed that LATE possesses transcriptional repression ability, which appears to be attributable to both the EAR motif and other sequences. Yeast two-hybrid assay showed the EAR motif-mediated interaction of LATE with TOPLESS, a transcriptional corepressor. Moreover, LATE could also interact with CRABS CLAW (CRC), one of the most important regulators of floral meristem determinacy, through sequences in LATE other than the EAR motif. Our findings demonstrated the possibility that LATE can form a transcriptional repression complex with CRC for floral meristem determinacy.
在正确的时间形成正确的花器官是植物实现繁殖成功的最重要策略之一。已知晚花(LATE)的异位过表达会诱导晚花,部分原因是通过抑制拟南芥中开花素编码基因()的表达。LATE是C2H2锌指转录因子之一,在其C末端末尾具有一个典型的转录抑制结构域,称为乙烯响应元件结合因子相关两亲性抑制(EAR)基序。因此,LATE被认为是一种转录抑制因子,但其分子功能仍不清楚。我们的基因组编辑突变体即使在开花时也没有表现出明显的表型,这表明存在来自其他因子的冗余。为了揭示LATE及其协同作用因子的分子功能,我们研究了它的转录活性以及与其他蛋白质的相互作用。反式激活活性分析表明,LATE具有转录抑制能力,这似乎归因于EAR基序和其他序列两者。酵母双杂交分析表明,LATE通过EAR基序介导与转录共抑制因子TOPLESS相互作用。此外,LATE还可以通过LATE中除EAR基序之外的序列与花分生组织确定性的最重要调节因子之一CRABS CLAW(CRC)相互作用。我们的研究结果证明了LATE可能与CRC形成转录抑制复合物以控制花分生组织确定性的可能性。