4.7 Article

Physiological responses and differential gene expression in Prunus rootstocks under iron deficiency conditions

期刊

JOURNAL OF PLANT PHYSIOLOGY
卷 168, 期 9, 页码 887-893

出版社

ELSEVIER GMBH
DOI: 10.1016/j.jplph.2010.11.017

关键词

Ferric chelate reductase; Iron chlorosis; Proton extrusion; qRT-PCR

资金

  1. MICINN (Spanish Ministry of Science and Innovation) [AGL 2008-00283]
  2. FEDER
  3. DGA (Diputacion General de Aragon) [A44]
  4. CSIC-FSE [I3P-PC2006]

向作者/读者索取更多资源

Two Prunus rootstocks, the Myrobalan plum P2175 and the interspecific peach-almond hybrid, Felinem, were studied to characterize their biochemical and molecular responses induced under iron-Deficient conditions. Plants of both genotypes were submitted to different treatments using a hydroponic system that permitted removal of Fe from the nutrient solution. Control plants were grown in 90 mu M Fe (III)-EDTA, Deficient plants were grown in an iron free solution, and plants submitted to an Inductor treatment were resupplied with 180 mu M Fe (III)-EDTA over 1 and 2 days after a period of 4 or 15 days of growth on an iron-free solution. Felinem increased the activity of the iron chelate reductase (FC-R) in the Inductor treatment after 4 days of iron deprivation. In contrast, P2175 did not show any response after at least 15 days without iron. The induction of the FC-R activity in this genotype was coincident in time with the medium acidification. These results suggest two different mechanisms of iron chlorosis tolerance in both Strategy! genotypes. Felinem would use the iron reduction as the main mechanism to capture the iron from the soil, and in P2175, the mechanism of response would be slower and start with the acidification of the medium synchronized with the gradual loss of chlorophyll in leaves. To better understand the control of these responses at the molecular level, the differential expression of PFRO2, PIRT1 and PAHA2 genes involved in the reductase activity, the iron transport in roots, and the proton release, respectively, were analyzed. The expression of these genes, estimated by quantitative real-time PCR, was different between genotypes and among treatments. The results were in agreement with the physiological responses observed. (C) 2011 Elsevier GmbH. All rights reserved.

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