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dc.contributor.authorZheng, Jianshu
dc.contributor.authorHong, Kai
dc.contributor.authorZeng, Longjun
dc.contributor.authorWang, Lei
dc.contributor.authorKang, Shujing
dc.contributor.authorQu, Minghao
dc.contributor.authorDai, Jiarong
dc.contributor.authorZou, Linyuan
dc.contributor.authorZhu, Lixin
dc.contributor.authorTang, Zhanpeng
dc.contributor.authorMeng, Xiangbing
dc.contributor.authorWang, Bing
dc.contributor.authorHu, Jiang
dc.contributor.authorZhao, Yonghui
dc.contributor.authorZeng, Dali
dc.contributor.authorCui, Peng
dc.contributor.authorWang, Quan
dc.contributor.authorQian, Qian
dc.contributor.authorWang, Yonghong
dc.contributor.authorLi, Jiayang
dc.contributor.authorXiong, Guosheng
dc.date.accessioned2020-07-20T08:02:46Z
dc.date.available2020-07-20T08:02:46Z
dc.date.issued2020-07-14
dc.date.submitted2020-02-24
dc.identifier.citationZheng, J., Hong, K., Zeng, L., Wang, L., Kang, S., Qu, M., … Xiong, G. (2020). Karrikin Signaling Acts Parallel to and Additively with Strigolactone Signaling to Regulate Rice Mesocotyl Elongation in Darkness. The Plant Cell, tpc.00123.2020. doi:10.1105/tpc.20.00123
dc.identifier.issn1040-4651
dc.identifier.pmid32665307
dc.identifier.doi10.1105/tpc.20.00123
dc.identifier.urihttp://hdl.handle.net/10754/664281
dc.description.abstractSeedling emergence in monocots depends mainly on mesocotyl elongation, requiring the coordination between developmental signals and environmental stimuli. Strigolactones (SLs) and karrikins are butenolide compounds that regulate various developmental processes; both are able to negatively regulate rice (Oryza sativa) mesocotyl elongation in the dark. Here, we report that a karrikin signaling complex, DWARF 14-LIKE (D14L)-DWARF 3 (D3)-Oryza sativa SUPPRESSOR OF MAX2 1 (OsSMAX1), regulates rice mesocotyl elongation in the dark. We demonstrate that D14L recognizes the karrikin signal and recruits the SCFD3 ubiquitin ligase for the ubiquitination and degradation of OsSMAX1, mirroring the SL-induced and D14- and D3-dependent ubiquitination and degradation of D53. Overexpression of OsSMAX1 promoted mesocotyl elongation in the dark, whereas knockout of OsSMAX1 suppressed the elongated-mesocotyl phenotypes of d14l and d3 but had little effect on their shoot branching phenotype. OsSMAX1 localizes in nucleus and interacts with TOPLESS-RELATED PROTEINs (TPRs), regulating downstream gene expression. Moreover, we showed that the GR24 enantiomers GR245DS and GR24ent-5DS specifically inhibit mesocotyl elongation and regulate downstream gene expression in a D14- and D14L-dependent manner, respectively. Our work revealed that karrikin and SL signaling play parallel and additive roles in modulating downstream genes expression and negatively regulating mesocotyl elongation in the dark.
dc.description.sponsorshipWe thank Prof. Shengben Li of Nanjing Agricultural University and Prof. Zhixi Tian of Institute of Genetics and Developmental Biology, Chinese academy of Sciences for critical reading. We thank Prof. Qi Xie of the Institute of Genetics and Developmental Biology, Chinese Academy of Sciences for providing the antibody of ubiquitin. We thank High-Performance Computing Centers at Agricultural Genomics Institute at Shenzhen, CAAS for bioinformatics support and also thank Jiangsu Collaborative Innovation Center for Modern Crop Production for support. This work was supported by founding from National Key Research and Development Program of China (2016YFD0101801), National Natural Science Foundation of China (31501384 and 31201004) and Science, Technology and Innovation Commission of Shenzhen Municipality (JCYJ20170303154319837, JCYJ20170412155447658, and KQJSCX2018323140312935).
dc.publisherAmerican Society of Plant Biologists (ASPB)
dc.relation.urlhttp://www.plantcell.org/lookup/doi/10.1105/tpc.20.00123
dc.rightsArchived with thanks to The Plant cell
dc.titleKarrikin Signaling Acts Parallel to and Additively with Strigolactone Signaling to Regulate Rice Mesocotyl Elongation in Darkness.
dc.typeArticle
dc.contributor.departmentComputational Bioscience Research Center (CBRC)
dc.contributor.departmentDesert Agriculture Initiative
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentComputer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division
dc.identifier.journalThe Plant cell
dc.eprint.versionPre-print
dc.contributor.institutionAgricultural Genomics Institute at Shenzhen CITY: Shenzhen China [CN]
dc.contributor.institutionInstitute of Plant Physiology & Ecology, Shanghai Institutes for Biological Sciences, CAS CITY: Shanghai China [CN]
dc.contributor.institutionInstitute of Genetics and Developmental Biology, Chinese Academy of Sciences CITY: Beijing China [CN]
dc.contributor.institutionNanjing Agricultural University CITY: Nanjing China [CN]
dc.contributor.institutionChina National Rice Research Institute CITY: Hangzhou China [CN]
dc.contributor.institutioncnrri CITY: HangZhou STATE: Zh POSTAL_CODE: 310006 China [CN]
dc.contributor.institutionNanjing Agricultural University CITY: Nanjing STATE: Jiangsu China [CN]
dc.contributor.institutionState Key Laboratory of Rice Biology, China National Rice Research Institute, Chinese Academy of Agricultural Sciences CITY: Hangzhou China [CN]
dc.contributor.institutionInstitute of Genetics and Developmental Biology, Chinese Academy of Sciences CITY: Beijing POSTAL_CODE: 100101 China [CN]
dc.contributor.institutionNanjing agricultrual University CITY: Nanjing China [CN]
dc.identifier.pagestpc.00123.2020
kaust.personCui, Peng
dc.date.accepted2020-07-09
dc.date.published-online2020-07-14
dc.date.published-print2020-09


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