4.7 Article

Salt-induced expression of genes related to Na+/K+ and ROS homeostasis in leaves of salt-resistant and salt-sensitive poplar species

Journal

PLANT MOLECULAR BIOLOGY
Volume 73, Issue 3, Pages 251-269

Publisher

SPRINGER
DOI: 10.1007/s11103-010-9612-9

Keywords

Affymetrix poplar genome array; NaCl; Populus euphratica; P. popularis; Salt tolerance

Funding

  1. HI-TECH Research and Development Programme of China [2006AA10Z131]
  2. National Natural Science Foundation of China [30430430, 30872005]
  3. Foundation for Supervisors of Beijing Excellent Doctoral Dissertations [YB20081002201]
  4. Foundation for Authors of the National Excellent Doctoral Dissertation of PR China [200152]
  5. Teaching and Research Award Programme for Outstanding Young Teachers at Higher Education Institutions of the Ministry of Education (MOE), PRC [2002-323, 2009-84]
  6. Natural Science Foundation of Hubei Province [2007ABB003]

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Using the Affymetrix poplar genome array, we explored the leaf transcriptome of salt-tolerant Populus euphratica Oliv. and salt-sensitive P. popularis 35-44 (P. popularis) under control and saline conditions. Our objective was to clarify the genomic differences in regulating K+/Na+ and reactive oxygen species (ROS) homeostasis between the two species. Compared to P. popularis, salt-tolerant P. euphratica responses to salinity involved induction of a relatively larger number of probesets after short-term (ST) exposure to 150 mM NaCl (24 h) and relatively fewer probesets after a long-term (LT) exposure to salinity (200 mM NaCl, 28 days). Compared to P. popularis, leaves of the control P. euphratica plants exhibited a higher transcript abundance of genes related to Na+/H+ antiport (Na+/H+ antiporters, H+ pumps) and K+ uptake and transport. Notably, the expression of these genes did not decrease (with a few exceptions) during salt treatment. Regarding ROS homeostasis, P. euphratica exhibited rapid up-regulation of a variety of antioxidant enzymes after exposure to ST salinity, indicating a rapid adaptive response to salt stress. However, the effect of NaCl on transcription in P. popularis leaves was more pronounced after exposure to prolonged salinity. LT-stressed P. popularis up-regulated some genes mediating K+/Na+ homeostasis but decreased transcription of main scavengers of superoxide radicals and H2O2 except for some isoforms of a few scavengers. Mineral and ROS analyses show that NaCl induced a marked increase of leaf Na+ and H2O2 in LT-stressed plants of the two species and the effects were even more pronounced in the salt-sensitive poplar. We place the transcription results in the context of our physiological measurements to infer some implications of NaCl-induced alterations in gene expression related to K+/Na+ and ROS homeostasis.

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