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BBX32抑制E3连接酶活性以促进新出土幼苗的变绿。

BBX32 dampens E3 ligase activity to promote greening in emerging seedlings.

作者信息

Wang Kangwei, Meng Yun, Tian Qian, Zhou Rong, Wu Shi-An, Wu Jiashuai, Sajid Shameen, He Ying, Ling Junjie, Jiang Haiyang, Wu Qingqing

机构信息

National Engineering Laboratory of Crop Stress Resistance Breeding, School of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.

出版信息

J Integr Plant Biol. 2025 Aug;67(8):2078-2099. doi: 10.1111/jipb.13939. Epub 2025 May 30.

DOI:10.1111/jipb.13939
PMID:40444488
Abstract

Germinating seeds undergo elaborate de-etiolation developmental transitions upon initial soil emergence. As central transcription factors promoting cotyledon greening, the abundance of ETHYLENE-INSENSITIVE 3 (EIN3) and PHYTOCHROME-INTERACTING FACTOR 3 (PIF3) are strictly controlled by physically associating themselves with the EIN3-BINDING F BOX PROTEINS 1 and 2 (EBF1/2) for ubiquitination. Here, we report that the B-box zinc-finger protein BBX32, as a positive regulator during seedling de-etiolation. BBX32 is robustly elevated during the dark-to-light transitions. Constitutively expressing BBX32 ultimately protects against severe photobleaching damage by synchronizing the accumulation of protochlorophyllide (Pchlide) and the differentiation of etioplast-chloroplast apparatus in buried seedlings. Specifically, BBX32 directly interacts with EIN3, PIF3 and EBF1/2. These associations disrupt the assembly of the SCF-EIN3/PIF3 E3 ligation protein complexes, thus dampening E3 ligase activity and robustly controlling EIN3/PIF3 stability. Under soil conditions, BBX32-ox largely rescues the greening deficiency of EBF1ox, and all EIN3ox/bbx32 seedlings override the bbx32 mutant defect and successfully turn green. Both biochemical findings and genetic evidence reveal a novel regulatory paradigm by which the B-box protein dampens the E3 ligase binding activity to achieve green seedlings upon changes in light or soil environmental conditions.

摘要

萌发的种子在最初出土后会经历复杂的去黄化发育转变。作为促进子叶绿化的核心转录因子,乙烯不敏感3(EIN3)和光敏色素相互作用因子3(PIF3)的丰度通过与EIN3结合F盒蛋白1和2(EBF1/2)物理结合进行泛素化而受到严格控制。在此,我们报道B-box锌指蛋白BBX32作为幼苗去黄化过程中的正调控因子。在从黑暗到光照的转变过程中,BBX32显著升高。组成型表达BBX32最终通过同步原叶绿素酸酯(Pchlide)的积累和埋入土中的幼苗中黄化质体-叶绿体装置的分化来防止严重的光漂白损伤。具体而言,BBX32直接与EIN3、PIF3和EBF1/2相互作用。这些相互作用破坏了SCF-EIN3/PIF3 E3连接蛋白复合物的组装,从而减弱E3连接酶活性并严格控制EIN3/PIF3的稳定性。在土壤条件下,BBX32过表达在很大程度上挽救了EBF1过表达的绿化缺陷,并且所有EIN3过表达/bbx32幼苗克服了bbx32突变体缺陷并成功变绿。生化研究结果和遗传证据都揭示了一种新的调控模式,即B-box蛋白通过减弱E3连接酶结合活性,在光照或土壤环境条件变化时实现幼苗变绿。

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