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BMC Genomics  2012 

Genome-wide microarray analysis of tomato roots showed defined responses to iron deficiency

DOI: 10.1186/1471-2164-13-101

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Abstract:

A genome-wide transcriptional analysis, performed with a chip that allows to monitor the expression of more than 25,000 tomato transcripts, identified 97 differentially expressed transcripts by comparing roots of Fe-deficient and Fe-sufficient tomato plants. These transcripts are related to the physiological responses of tomato roots to the nutrient stress resulting in an improved iron uptake, including regulatory aspects, translocation, root morphological modification and adaptation in primary metabolic pathways, such as glycolysis and TCA cycle. Other genes play a role in flavonoid biosynthesis and hormonal metabolism.The transcriptional characterization confirmed the presence of the previously described mechanisms to adapt to iron starvation in tomato, but also allowed to identify other genes potentially playing a role in this process, thus opening new research perspectives to improve the knowledge on the tomato root response to the nutrient deficiency.Iron (Fe) deficiency is a yield-limiting factor for a variety of field crops all around the world and generally results from the interaction of limited soil Fe bioavailability and susceptible genotype cultivation [1]. Iron is an important microelement for plant life due to its involvement as redox-active metal in photosynthesis, mitochondrial respiration, nitrogen assimilation, hormone biosynthesis, production and scavenging of reactive oxygen species, osmoprotection and pathogen defence [2].Under aerated conditions at neutral alkaline pH, the soluble Fe concentration in soil solution is very low. To cope with Fe shortage plants have developed two strategies for its acquisition. The Strategy I (all higher plants except grasses) relies on improvement of Fe uptake through acidification of soil solution by excretion of protons via a plasmalemma P-type ATPase resulting in an increased Fe solubility, reduction of Fe3+ to the more soluble Fe2+ by a FeIII-chelate reductase and plasmalemma transport of Fe2+ by the activity

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