Nucleotide-binding site leucine-rich repeat receptors (NBS-LRR/NLRs) are crucial intracellular immune proteins in plants. Previous article reported a novel NLR protein SUT1 (SUPPRESSORS OF TOPP4-1, 1), which is involv...Nucleotide-binding site leucine-rich repeat receptors (NBS-LRR/NLRs) are crucial intracellular immune proteins in plants. Previous article reported a novel NLR protein SUT1 (SUPPRESSORS OF TOPP4-1, 1), which is involved in autoimmunity initiated by type one protein phosphatase 4 mutation (topp4-1) in Arabidopsis, however, its role in planta is still unclear. This study employed Nicotiana benthamiana, a model platform, to conduct an overall structural and functional analysis of SUT1 protein. The transient expression results revealed that SUT1 is a typical CNL (CC-NBS-LRR) receptor, both fluorescence data and biochemical results showed the protein is mainly anchored on the plasma membrane due to its N-terminal acylation site. Further truncation experiments announced that its CC (coiled-coil) domain possessed cell-death-inducing activity. The outcomes of point mutations analysis revealed that not only the CC domain, but also the full-length SUT1 protein, whose function and subcellular localization are influenced by highly conserved hydrophobic residues. These research outcomes provided favorable clues for elucidating the activation mechanism of SUT1.展开更多
Research background: The Arabidopsis-resistance protein L5 (AT1G12290) can trigger cell death in Nicotiana benthamiana, which is a characteristic function of an NBS-LRR (Nucleotide-Binding Sites and Leucine-Rich Repea...Research background: The Arabidopsis-resistance protein L5 (AT1G12290) can trigger cell death in Nicotiana benthamiana, which is a characteristic function of an NBS-LRR (Nucleotide-Binding Sites and Leucine-Rich Repeat) protein activation. Purpose: To explore the function and molecular regulatory network of L5. Method: We employed yeast two-hybrid technology to search for interacting proteins of L5, combined with laser confocal microscopy to observe the subcellular localization of these candidate proteins, and analyzed the impact of these proteins on L5 function using an Agrobacterium mediated transient expression system. Results: Seven candidate interacting proteins were identified from the Arabidopsis cDNA library, including PPA1 (AT1G01050), RIN4 (AT3G25070), LSU1 (AT3G49580), BZIP24 (AT3G51960), BOI (AT4G19700), RING/U (AT4G22250) and PPA3 (AT2G46860). Functional analysis of these candidate interacting proteins showed that they participated in multiple pathways, including biological and abiotic stress, programmed cell death, protein degradation, material metabolism and transcriptional regulation. The results of laser confocal microscopy manifested that RIN4 was only localized on the plasma membrane (PM), and RING/U was mainly associated with the PM. PPA1, PPA3, LSU1, BZIP24, and BOI all emerged nuclear and cytoplasmic localization. The results of the transient assay proclaimed that both BOI and RING/U can inhibit cell death caused by L5. Conclusions: These results indicate that L5 immune receptors may participate in various pathways, and their protein levels and activities are strictly regulated at multiple levels, providing a basis for elucidating the mechanism of L5 immune receptors in Arabidopsis resistance.展开更多
目的为解析党参NBS-LRR(Nucleotide-binding site and leucine-rich repeat)抗病基因家族,探究党参抗根腐病机制,从而解决党参根腐病害难题,促进党参育种及产业发展。方法基于党参响应根腐病病原菌的转录组数据,通过运用生物信息学方法...目的为解析党参NBS-LRR(Nucleotide-binding site and leucine-rich repeat)抗病基因家族,探究党参抗根腐病机制,从而解决党参根腐病害难题,促进党参育种及产业发展。方法基于党参响应根腐病病原菌的转录组数据,通过运用生物信息学方法对党参NBS-LRR家族基因进行理化性质、基因结构、系统发育、表达模式及互作网络分析。结果成功鉴定到88个党参NBS-LRR家族基因,包括N、NL、CN、CNL、TN、TNL、PN共7种类型,分别有50、14、1、14、4、3、2个基因。结果表明,党参CNL及TNL类基因结构比较保守;党参CNL亚家族基因在进化过程中发生扩增;党参NBS-LRR家族基因在尖孢镰刀菌(Fusarium oxysporum)侵染条件下存在时间表达模式差异,且侵染前期(6-24 h)高表达的基因DN64786c1g6、DN64786c1g5、DN48234c0g2、DN54844c1g2、DN59747c0g3、DN56071c1g8、DN64591c1g1、DN48464c1g1、DN59886c0g1在调控党参抗病过程中发挥重要作用。其中党参的抗病蛋白DN54844c1g2可能与GLR家族互作,进而通过调节Ca2+内流参与免疫调控;DN64786c1g5可能与CYTC-1和CYTC-2互作,进而通过参与氧化还原反应参与党参响应根腐病过程;DN59747c0g3可能与MPK3互作,进而通过参与MAP信号级联、磷酸化WRKY转录因子以及参与超敏反应(HR),在党参响应根腐病过程中发挥重要作用。结论党参NBSLRR家族基因的鉴定及表达分析对于探究党参抗根腐病机制、发掘基因功能具有重要意义。展开更多
NBS-LRR(nucleotide-binding site and leucine-rich-repeat)是植物中最大类抗病基因家族之一。番茄基因组测序完成为全基因组水平上分析NBS-LRR抗病基因家族提供了机遇。利用生物信息学方法对番茄NBS-LRR抗病基因家族成员数目进行鉴定...NBS-LRR(nucleotide-binding site and leucine-rich-repeat)是植物中最大类抗病基因家族之一。番茄基因组测序完成为全基因组水平上分析NBS-LRR抗病基因家族提供了机遇。利用生物信息学方法对番茄NBS-LRR抗病基因家族成员数目进行鉴定,并对其染色体定位和系统发育关系进行了分析。随后,将番茄和马铃薯NBS-LRR抗病基因进行了比较基因组学分析。结果表明:番茄基因组共包括252个NBS-LRR抗病基因,分布于番茄12条染色体上;63.5%的基因成簇存在,大部分为串联重复;系统发育关系分析表明番茄CC-NBS-LRR(CNL)亚家族较其他亚家族扩展程度大;同线性分析发现番茄中共79个NBS-LRR抗病基因与马铃薯基因具有同源关系。结果将为番茄NBS-LRR抗病基因家族的深入研究提供依据,同时也为利用番茄NBS-LRR基因进行基因定位以及相关抗病基因克隆等奠定基础。展开更多
文摘Nucleotide-binding site leucine-rich repeat receptors (NBS-LRR/NLRs) are crucial intracellular immune proteins in plants. Previous article reported a novel NLR protein SUT1 (SUPPRESSORS OF TOPP4-1, 1), which is involved in autoimmunity initiated by type one protein phosphatase 4 mutation (topp4-1) in Arabidopsis, however, its role in planta is still unclear. This study employed Nicotiana benthamiana, a model platform, to conduct an overall structural and functional analysis of SUT1 protein. The transient expression results revealed that SUT1 is a typical CNL (CC-NBS-LRR) receptor, both fluorescence data and biochemical results showed the protein is mainly anchored on the plasma membrane due to its N-terminal acylation site. Further truncation experiments announced that its CC (coiled-coil) domain possessed cell-death-inducing activity. The outcomes of point mutations analysis revealed that not only the CC domain, but also the full-length SUT1 protein, whose function and subcellular localization are influenced by highly conserved hydrophobic residues. These research outcomes provided favorable clues for elucidating the activation mechanism of SUT1.
文摘Research background: The Arabidopsis-resistance protein L5 (AT1G12290) can trigger cell death in Nicotiana benthamiana, which is a characteristic function of an NBS-LRR (Nucleotide-Binding Sites and Leucine-Rich Repeat) protein activation. Purpose: To explore the function and molecular regulatory network of L5. Method: We employed yeast two-hybrid technology to search for interacting proteins of L5, combined with laser confocal microscopy to observe the subcellular localization of these candidate proteins, and analyzed the impact of these proteins on L5 function using an Agrobacterium mediated transient expression system. Results: Seven candidate interacting proteins were identified from the Arabidopsis cDNA library, including PPA1 (AT1G01050), RIN4 (AT3G25070), LSU1 (AT3G49580), BZIP24 (AT3G51960), BOI (AT4G19700), RING/U (AT4G22250) and PPA3 (AT2G46860). Functional analysis of these candidate interacting proteins showed that they participated in multiple pathways, including biological and abiotic stress, programmed cell death, protein degradation, material metabolism and transcriptional regulation. The results of laser confocal microscopy manifested that RIN4 was only localized on the plasma membrane (PM), and RING/U was mainly associated with the PM. PPA1, PPA3, LSU1, BZIP24, and BOI all emerged nuclear and cytoplasmic localization. The results of the transient assay proclaimed that both BOI and RING/U can inhibit cell death caused by L5. Conclusions: These results indicate that L5 immune receptors may participate in various pathways, and their protein levels and activities are strictly regulated at multiple levels, providing a basis for elucidating the mechanism of L5 immune receptors in Arabidopsis resistance.
文摘目的为解析党参NBS-LRR(Nucleotide-binding site and leucine-rich repeat)抗病基因家族,探究党参抗根腐病机制,从而解决党参根腐病害难题,促进党参育种及产业发展。方法基于党参响应根腐病病原菌的转录组数据,通过运用生物信息学方法对党参NBS-LRR家族基因进行理化性质、基因结构、系统发育、表达模式及互作网络分析。结果成功鉴定到88个党参NBS-LRR家族基因,包括N、NL、CN、CNL、TN、TNL、PN共7种类型,分别有50、14、1、14、4、3、2个基因。结果表明,党参CNL及TNL类基因结构比较保守;党参CNL亚家族基因在进化过程中发生扩增;党参NBS-LRR家族基因在尖孢镰刀菌(Fusarium oxysporum)侵染条件下存在时间表达模式差异,且侵染前期(6-24 h)高表达的基因DN64786c1g6、DN64786c1g5、DN48234c0g2、DN54844c1g2、DN59747c0g3、DN56071c1g8、DN64591c1g1、DN48464c1g1、DN59886c0g1在调控党参抗病过程中发挥重要作用。其中党参的抗病蛋白DN54844c1g2可能与GLR家族互作,进而通过调节Ca2+内流参与免疫调控;DN64786c1g5可能与CYTC-1和CYTC-2互作,进而通过参与氧化还原反应参与党参响应根腐病过程;DN59747c0g3可能与MPK3互作,进而通过参与MAP信号级联、磷酸化WRKY转录因子以及参与超敏反应(HR),在党参响应根腐病过程中发挥重要作用。结论党参NBSLRR家族基因的鉴定及表达分析对于探究党参抗根腐病机制、发掘基因功能具有重要意义。
文摘NBS-LRR(nucleotide-binding site and leucine-rich-repeat)是植物中最大类抗病基因家族之一。番茄基因组测序完成为全基因组水平上分析NBS-LRR抗病基因家族提供了机遇。利用生物信息学方法对番茄NBS-LRR抗病基因家族成员数目进行鉴定,并对其染色体定位和系统发育关系进行了分析。随后,将番茄和马铃薯NBS-LRR抗病基因进行了比较基因组学分析。结果表明:番茄基因组共包括252个NBS-LRR抗病基因,分布于番茄12条染色体上;63.5%的基因成簇存在,大部分为串联重复;系统发育关系分析表明番茄CC-NBS-LRR(CNL)亚家族较其他亚家族扩展程度大;同线性分析发现番茄中共79个NBS-LRR抗病基因与马铃薯基因具有同源关系。结果将为番茄NBS-LRR抗病基因家族的深入研究提供依据,同时也为利用番茄NBS-LRR基因进行基因定位以及相关抗病基因克隆等奠定基础。
