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DC Field | Value | Language |
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dc.contributor.author | Saxena, Saurabh C. | - |
dc.contributor.author | Salvi, Prafull | - |
dc.contributor.author | Kaur, Harmeet | - |
dc.contributor.author | Verma, Pooja | - |
dc.contributor.author | Petla, Bhanu Prakash | - |
dc.contributor.author | Rao, Venkateswara | - |
dc.contributor.author | Kamble, Nitin | - |
dc.contributor.author | Majee, Manoj | - |
dc.date.accessioned | 2015-11-18T07:09:24Z | - |
dc.date.available | 2015-11-18T07:09:24Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | J. Exp. Bot., 64(18): 5623-5639 | en_US |
dc.identifier.issn | 1460-2431 | - |
dc.identifier.uri | http://172.16.0.77:8080/jspui/handle/123456789/363 | - |
dc.description | Accepted date: 5 September 2013 | en_US |
dc.description.abstract | myo-Inositol monophosphatase (IMP) is an essential enzyme in the myo-inositol metabolic pathway where it primarily dephosphorylates myo-inositol 1-phosphate to maintain the cellular inositol pool which is important for many metabolic and signalling pathways in plants. The stress-induced increased accumulation of inositol has been reported in a few plants including chickpea; however, the role and regulation of IMP is not well defined in response to stress. In this work, it has been shown that IMP activity is distributed in all organs in chickpea and was noticeably enhanced during environmental stresses. Subsequently, using degenerate oligonucleotides and RACE strategy, a full-length IMP cDNA (CaIMP) was cloned and sequenced. Biochemical study revealed that CaIMP encodes a lithium-sensitive phosphatase enzyme with broad substrate specificity, although maximum activity was observed with the myo-inositol 1-phosphate and l-galactose 1-phosphate substrates. Transcript analysis revealed that CaIMP is differentially expressed and regulated in different organs, stresses and phytohormones. Complementation analysis in Arabidopsis further confirmed the role of CaIMP in l-galactose 1-phosphate and myo-inositol 1-phosphate hydrolysis and its participation in myo-inositol and ascorbate biosynthesis. Moreover, Arabidopsis transgenic plants over-expressing CaIMP exhibited improved tolerance to stress during seed germination and seedling growth, while the VTC4/IMP loss-of-function mutants exhibited sensitivity to stress. Collectively, CaIMP links various metabolic pathways and plays an important role in improving seed germination and seedling growth, particularly under stressful environments. | en_US |
dc.description.sponsorship | This work was supported by the Department of Biotechnology, Government of India under the scheme of the ‘Next generation Challenge Programme in Chickpea Genomics’ (Grant no: BT/PR12919/AGR/02/676/2009). PS, HK, BP, VR, NK, and PV thank the Council of Scientific and Industrial Research and the University Grant Commission, Government of India, for research fellowships. We are grateful to Dr Glenda Gillaspy, Virginia Tech. USA for providing us with the vtc4 mutants (vtc4-3:SAIL_843_G10 and vtc4-4:SALK_077222). | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Oxford University Press | en_US |
dc.subject | Ascorbate | en_US |
dc.subject | gluconeogenesis | en_US |
dc.subject | inositol | en_US |
dc.subject | multifunctional | en_US |
dc.subject | phosphatase | en_US |
dc.subject | seed germination | en_US |
dc.subject | stress tolerance | en_US |
dc.title | Differentially expressed myo-inositol monophosphatase gene (CaIMP) in chickpea (Cicer arietinum L.) encodes a lithium-sensitive phosphatase enzyme with broad substrate specificity and improves seed germination and seedling growth under abiotic stresses | en_US |
dc.type | Article | en_US |
dc.identifier.officialurl | http://jxb.oxfordjournals.org/content/64/18/5623.long | en_US |
dc.identifier.doi | 10.1093/jxb/ert336 | en_US |
Appears in Collections: | Institutional Publications |
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Majee M_2013_4.pdf Restricted Access | 5.54 MB | Adobe PDF | View/Open Request a copy |
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