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The KNAT3a1-WND2A/3A module positively regulates fiber secondary cell wall biosynthesis in Populus tomentosa
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作者 Kuan Sun Di Fan +7 位作者 Yingying Peng Chang Liu Lingfei Kong Ting Lan Xianqiang Wang Dan Li Chaofeng Li Keming Luo 《Horticultural Plant Journal》 2025年第3期1326-1340,共15页
The secondary cell wall(SCW)is essential for plant growth and development in vascular plants,and its biosynthesis is mainly controlled by a complex hierarchical regulatory network involving multiple transcription fact... The secondary cell wall(SCW)is essential for plant growth and development in vascular plants,and its biosynthesis is mainly controlled by a complex hierarchical regulatory network involving multiple transcription factors(TFs)at the transcription level.However,TFs that specifically regulate secondary xylem have not been widely reported.In this study,we described a poplar KNOTTED1-like homeobox(KNOX)TF PtoKNAT3a1,which was mainly expressed in the expanding xylem cells of stems.PtoKNAT3a1 overexpression caused fiber SCW thickening and increased all measured SCW compositions by upregulating the expression of SCW-biosynthetic genes and-associated TFs,but had no effect on the vessels of SCW.The opposite phenotype was observed in the PtoKNAT3a1-knockout lines.Hence,we further demonstrated that Pto-KNAT3a1 could physically interact with the NAC master switches PtoWND2A/3A to enhance the expression of downstream MYB TFs and SCW biosynthetic genes(including PtoMYB20,PtoMYB21,PtoMYB90,PtoCoMT2,PtoGT43B and PtoCesA8).Meanwhile,the studies also demonstrate that the KNAT3 has functional differentiation in xylem development.Taken together,these data suggest that the KNAT3a1-WND2A/3A module positively regulates fiber development of the secondary xylem in poplar via the WND2A/3A-mediated hierarchical regulatory network,and supplies useful information for fiber SCW formation.The research not only deepens the understanding of the hierarchical regulatory network affecting SCW formation but also supplies genetic resources and molecular targets for plant fiber utilization. 展开更多
关键词 Fiber secondary cell wall knat transcription factor Secondary xylem MODULE Hierarchical regulatory network
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Requirement of KNAT1/BP for the Development of Abscission Zones in Arabidopsis thaliana 被引量:10
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作者 Xiao-Qun Wang Wei-Hui Xu +4 位作者 Li-Geng Ma Zhi-Ming Fu Xing-Wang Deng Jia-Yang Li Yong-Hong Wang 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2006年第1期15-26,共12页
The KNAT1 gene is a member of the Class I KNOXhomeobox gene family and is thought to play an important role in meristem development and leaf morphogenesis. Recent studies have demonstrated that KNAT1/BP regulates the ... The KNAT1 gene is a member of the Class I KNOXhomeobox gene family and is thought to play an important role in meristem development and leaf morphogenesis. Recent studies have demonstrated that KNAT1/BP regulates the architecture of the inflorescence by affecting pedicle development in Arabidopsis thaliana. Herein, we report the characterization of an Arabidopsis T-DNA insertion mutant that shares considerable phenotypic similarity to the previously identified mutant brevipedicle (bp). Molecular and genetic analyses showed that the mutant is allelic to bp and that the T-DNA is located within the first helix of the KNAT1 homeodomain (HD). Although the mutation causes a typical abnormality of short pedicles, propendent siliques, and semidwarfism, no obvious defects are observed in the vegetative stage. A study on cell morphology showed that asymmetrical division and inhibition of cell elongation contribute to the downward-pointing and shorter pedicle phenotype. Loss of KNAT/BPfunction results in the abnormal development of abscission zones. Mlcroarray analysis of gene expression profiling suggests that KNAT1/BP may regulate abscission zone development through hormone signaling and hormone metabolism in Arabidopsis. 展开更多
关键词 abscission zone Arabidopsis thaliana BP/knat1 MICROARRAY pedicle.
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拟南芥木聚糖合成关键酶基因的调控研究
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作者 王玉琪 贺俊波 吴蔼民 《华南农业大学学报》 CAS CSCD 北大核心 2014年第4期97-102,共6页
【目的】从目前已知的参与拟南芥Arabidopsis thaliana次生壁加厚生长的转录因子着手,分析这些次生壁相关的转录因子是否能够调控木糖合成关键酶基因FRA8、IRX9、IRX10、IRX14、F8H、IRX9-L、IRX10-L和IRX14-L的表达,并且观察KNAT7基因... 【目的】从目前已知的参与拟南芥Arabidopsis thaliana次生壁加厚生长的转录因子着手,分析这些次生壁相关的转录因子是否能够调控木糖合成关键酶基因FRA8、IRX9、IRX10、IRX14、F8H、IRX9-L、IRX10-L和IRX14-L的表达,并且观察KNAT7基因显性抑制植株的表型.【方法】通过Gateway技术构建效应器和报告器,进行瞬时转录激活试验,同样构建pCAMBIA1304-p35S∷KNAT7-SRDX重组质粒,用农杆菌Agrobacterium tumefaciens花序浸染法将此质粒转化到野生型拟南芥植株中.【结果和结论】瞬时转录激活试验表明,转录因子KNAT7、MYB46、ERF72、SND1、NST2能够激活多个拟南芥木聚糖合成关键酶基因的表达,其中KNAT7能促进基因FRA8、IRX9和IRX14-L的表达.KNAT7基因显性抑制能显著影响拟南芥的生长.试验结果表明KNAT7基因可能在木聚糖的合成中起着重要的调控作用. 展开更多
关键词 木聚糖 木聚糖合成关键酶基因 调控 knat7
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