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The NAC-like transcription factor Si NAC110 in foxtail millet(Setaria italica L.) confers tolerance to drought and high salt stress through an ABA independent signaling pathway 被引量:9
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作者 XIE Li-na CHEN Ming +7 位作者 MIN Dong-hong FENG Lu XU Zhao-shi ZHOU Yong-bin XU Dong-bei LI Lian-cheng MA You-zhi ZHANG Xiao-hong 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2017年第3期559-571,共13页
Foxtail millet(Setaria italica(L.)P.Beauv)is a naturally stress tolerant crop.Compared to other gramineous crops,it has relatively stronger drought and lower nutrition stress tolerance traits.To date,the scope of ... Foxtail millet(Setaria italica(L.)P.Beauv)is a naturally stress tolerant crop.Compared to other gramineous crops,it has relatively stronger drought and lower nutrition stress tolerance traits.To date,the scope of functional genomics research in foxtail millet(S.italic L.)has been quite limited.NAC(NAM,ATAF1/2 and CUC2)-like transcription factors are known to be involved in various biological processes,including abiotic stress responses.In our previous foxtail millet(S.italic L.)RNA seq analysis,we found that the expression of a NAC-like transcription factor,SiNAC110,could be induced by drought stress;additionally,other references have reported that SiNAC110 expression could be induced by abiotic stress.So,we here selected SiNAC110 for further characterization and functional analysis.First,the predicted SiNAC110 protein encoded indicated SiNAC110 has a conserved NAM(no apical meristem)domain between the 11–139 amino acid positions.Phylogenetic analysis then indicated that SiNAC110 belongs to subfamily III of the NAC gene family.Subcellular localization analysis revealed that the SiNAC110-GFP fusion protein was localized to the nucleus in Arabidopsis protoplasts.Gene expression profiling analysis indicated that expression of SiNAC110 was induced by dehydration,high salinity and other abiotic stresses.Gene functional analysis using SiNAC110 overexpressed Arabidopsis plants indicated that,under drought and high salt stress conditions,the seed germination rate,root length,root surface area,fresh weight,and dry weight of the SiNAC110 overexpressed lines were significantly higher than the wild type(WT),suggesting that the SiNAC110 overexpressed lines had enhanced tolerance to drought and high salt stresses.However,overexpression of SiN AC110 did not affect the sensitivity of SiNAC110 overexpressed lines to abscisic acid(ABA)treatment.Expression analysis of genes involved in proline synthesis,Na+/K+transport,drought responses,and aqueous transport proteins were higher in the SiNAC110overexpressed lines than in the WT,whereas expression of ABA-dependent pathway genes did not change.These results indicated that overexpression of SiNAC110 conferred tolerance to drought and high salt stresses,likely through influencing the regulation of proline biosynthesis,ion homeostasis and osmotic balance.Therefore,SiNAC110 appears to function in the ABA-independent abiotic stress response pathway in plants. 展开更多
关键词 foxtail millet (Setaria italica (L.) nac-like transcription factor drought stress high salt stress ABA-independent pathway
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N-乙酰半胱氨酸通过阻断Nrf2/Keap1通路抑制(H_(2)O_(2))处理的佐剂性关节炎成纤维细胞样滑膜细胞增殖 被引量:1
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作者 杨珺 黄焱平 +5 位作者 刘梅梅 汪陶荣 张晔 周文瀚 瞿子庭 陈晓宇 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2021年第8期687-692,共6页
目的探讨N-乙酰半胱氨酸(NAC)对低浓度过氧化氢(H_(2)O_(2))处理的佐剂性关节炎(AA)大鼠成纤维细胞样滑膜细胞(AA-FLS)增殖的影响及机制。方法SD大鼠分为正常对照组和模型组(均为10只),模型组采用足趾皮下注射Freund完全佐剂造模,28 d... 目的探讨N-乙酰半胱氨酸(NAC)对低浓度过氧化氢(H_(2)O_(2))处理的佐剂性关节炎(AA)大鼠成纤维细胞样滑膜细胞(AA-FLS)增殖的影响及机制。方法SD大鼠分为正常对照组和模型组(均为10只),模型组采用足趾皮下注射Freund完全佐剂造模,28 d后处死大鼠。硫代巴比妥酸法检测血清丙二醛(MDA)含量、羟胺法测定超氧化物歧化酶(SOD)活性,比色法测定谷胱甘肽过氧化物酶(GSH-Px)活性,免疫组织化学染色法检测踝关节滑膜组织中核因子E2相关因子2(Nrf2)、Kelch样ECH相关蛋白1(Keap1)蛋白表达;体外培养和鉴定AA-FLS,CCK-8法检测(0、0.3、0.9、3、10、30、90、180)μmol/L NAC对5μmol/L H_(2)O_(2)处理的AA-FLS活力的影响,采用MitoSOX线粒体活性氧荧光探针检测AA-FLS中线粒体活性氧(ROS)含量,Western blot法检测(0、3、10、30)μmol/L NAC对低浓度H_(2)O_(2)处理AA-FLS的Nrf2、Keap1蛋白表达的影响。结果与正常对照组比较,AA模型大鼠血清MDA水平增加、SOD、GSH-Px水平降低,滑膜组织中Nrf2表达升高、Keap1表达降低;免疫细胞化学染色证实分离培养的细胞是AA-FLS,NAC可浓度依赖性抑制H_(2)O_(2)处理的AA-FLS增殖,且线粒体ROS含量下降,Nrf2、Keap1蛋白表达降低。结论NAC可抑制H_(2)O_(2)处理后的AA-FLS增殖,其机制可能与阻断Nrf2/Keap1通路有关。 展开更多
关键词 N-乙酰半胱氨酸(NAC) 核因子E2相关因子2(Nrf2) Kelch样ECH相关蛋白1(Keap1) 氧化应激 佐剂性关节炎(AA) 成纤维细胞样滑膜细胞(FLS)
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