{"title":"BBX32 dampens E3 ligase activity to promote greening in emerging seedlings.","authors":"Kangwei Wang, Yun Meng, Qian Tian, Rong Zhou, Shi-An Wu, Jiashuai Wu, Shameen Sajid, Ying He, Junjie Ling, Haiyang Jiang, Qingqing Wu","doi":"10.1111/jipb.13939","DOIUrl":null,"url":null,"abstract":"<p><p>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<sup>EBF1/2</sup>-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.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":" ","pages":""},"PeriodicalIF":9.3000,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Integrative Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/jipb.13939","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
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 SCFEBF1/2-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.
期刊介绍:
Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.