首页> 外文期刊>Environmental Pollution >Lead exposure-induced defense responses result in low lead translocation from the roots to aerial tissues of two contrasting poplar species
【24h】

Lead exposure-induced defense responses result in low lead translocation from the roots to aerial tissues of two contrasting poplar species

机译:铅曝光诱导的防御反应导致从根部到两种对比的杨树物种的空中组织的低引导易位

获取原文
获取原文并翻译 | 示例
           

摘要

To explore whether lead (Pb)-induced defense responses are responsible for the low root-to-shoot Pb translocation, we exposed saplings of the two contrasting poplar species, Populus x canescens with relatively high root-to-shoot Pb translocation and P. nigra with low Pb translocation, to 0 or 8 mM PbCl2. Pb translocation from the roots to aboveground tissues was lower by 57% in P. nigra than that in P. x canescens. Lower Pb concentrations in the roots and aerial tissues, greater root biomass, and lower ROS overproduction in the roots were found in P. nigra than those in P. x canescens treated with Pb. P. nigra roots had higher proportions of cell walls (CWs)-bound Pb and water insoluble Pb compounds, and higher transcript levels of some pivotal genes related to Pb vacuolar sequestration, such as phytochelatin synthetase 1.1 (PCS1.1), ATP-binding cassette transporter C1.1 (ABCC1.1) and ABCC3.1 than P. x canescens roots. Pb exposure induced defense responses including increases in the contents of pectin and hemicellulose, and elevated oxalic acid accumulation, and the transcriptional upregulation of PCS1.1, ABCC1.1 and ABCC3.1 in the roots of P. nigra and P. x canescens. These results suggest that the stronger defense barriers in P. nigra roots are probably associated with the lower Pb translocation from the roots to aerial tissues, and that Pb exposure-induced defense responses can enhance the barriers against Pb translocation in poplar roots. (C) 2020 Elsevier Ltd. All rights reserved.
机译:为了探索铅(PB)诱导的防御反应是否负责低根芽PB易位,我们暴露了两种对比杨树种的树苗,杨树X小孔,具有相对高的根到射击PB易位和P. NIGRA低PB易位,到0或8 mm PBCL2。从根部到地上组织的Pb易位比P. nigra在x x泛孔中的下降57%。在根和空中组织中,较低的PB浓度,更大的根生物量,并在根中的X型X型X型胰岛素中的那些含量较低。 P. NIGRA根部具有较高的细胞壁(CWS) - 基因PB和水不溶性PB化合物,以及与PB真空螯合相关的一些枢轴基因的转录物水平,例如PHYTOCHELATIN合成酶1.1(PCS1.1),ATP结合盒式磁带转运仪C1.1(ABCC1.1)和ABCC3.1比P. x Canescens Roots。 PB曝光诱导的防御反应,包括果胶和半纤维素含量的增加,以及升高的草酸积累,以及PCS1.1,ABCC1.1和ABCC3.1的转录上调在P. nigra和P. x Canescens的根中。这些结果表明,P. NIGRA根中较强的防御障碍可能与从根到空中组织的较低的PB易位相关,并且PB暴露诱导的防御反应可以增强杨树根中PB易位的障碍。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Environmental Pollution》 |2021年第2期|116346.1-116346.11|共11页
  • 作者单位

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

    Nanjing Forestry Univ Coll Light Ind & Food Engn Dept Food Sci & Technol Nanjing 210037 Peoples R China;

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

    Chinese Acad Forestry Res Inst Forestry State Key Lab Tree Genet & Breeding Key Lab Silviculture State Forestry & Grassland A Beijing 100091 Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Heavy metal; cell wall; Chemical forms; Transcriptional regulation;

    机译:重金属;细胞壁;化学形式;转录调节;
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号