Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/495
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dc.contributor.authorChandra, A.-
dc.contributor.authorVerma, Praveen K.-
dc.contributor.authorIslam, M. N.-
dc.contributor.authorGrisham, M. P.-
dc.contributor.authorJain, R.-
dc.contributor.authorSharma, A.-
dc.contributor.authorRoopendra, K.-
dc.contributor.authorSingh, K.-
dc.contributor.authorSingh, P.-
dc.contributor.authorVerma, I.-
dc.contributor.authorSolomon, S.-
dc.date.accessioned2016-01-01T11:45:27Z-
dc.date.available2016-01-01T11:45:27Z-
dc.date.issued2015-
dc.identifier.citationPlant Biol., 17(3): 608-617en_US
dc.identifier.issn1435-8603-
dc.identifier.urihttp://172.16.0.77:8080/jspui/handle/123456789/495-
dc.descriptionAccepted date: 3 October 2014en_US
dc.description.abstractSucrose synthesis/accumulation in sugarcane is a complex process involving many genes and regulatory sequences that control biochemical events in source–sink tissues. Among these, sucrose synthase (SuSy), sucrose phosphate synthase (SPS), soluble acid (SAI) and cell wall (CWI) invertases are important. Expression of these enzymes was compared in an early (CoJ64) and late (BO91) maturing sugarcane variety using end-point and qRT-PCR. Quantitative RT-PCR at four crop stages revealed high CWI expression in upper internodes of CoJ64, which declined significantly in both top and bottom internodes with maturity. In BO91, CWI expression was high in top and bottom internodes and declined significantly only in top internodes as the crop matured. Overall, CWI expression was higher in CoJ64 than in BO91. During crop growth, there was no significant change in SPS expression in bottom internodes in CoJ64, whereas in BO91 it decreased significantly. Apart from a significant decrease in expression of SuSy in mature bottom internodes of BO91, there was no significant change. Similar SAI expression was observed with both end-point and RT-PCR, except for significantly increased expression in top internodes of CoJ64 with maturity. SAI, being a major sucrose hydrolysing enzyme, was also monitored with end-point PCR expression in internode tissues of CoJ64 and BO91, with higher expression of SAI in BO91 at early crop stages. Enzyme inhibitors, e.g. manganese chloride (Mn++), significantly suppressed expression of SAI in both early- and late-maturing varieties. Present findings enhance understanding of critical sucrose metabolic gene expression in sugarcane varieties differing in content and time of peak sucrose storage. Thus, through employing these genes, improvement of sugarcane sucrose content is possible.en_US
dc.description.sponsorshipThe authors are grateful to the directors of both institutes (IISR and NIPGR) for providing the necessary facilities and encouragement. We thank the NCBI and TIGR Plant Transcript Assemblies for making their databases available. Funding from DST, Government of India is duly acknowledged. We also thank two anonymous reviewers for critical comments and suggestions that significantly improved the article.en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectCell wall invertasesen_US
dc.subjectgene expressionen_US
dc.subjectheat mapen_US
dc.subjectsoluble aciden_US
dc.subjectsucrose phosphate synthaseen_US
dc.subjectsugarcaneen_US
dc.subjectsucrose synthaseen_US
dc.titleExpression analysis of genes associated with sucrose accumulation in sugarcane (Saccharum spp. hybrids) varieties differing in content and time of peak sucrose storageen_US
dc.typeArticleen_US
dc.identifier.officialurlhttp://onlinelibrary.wiley.com/doi/10.1111/plb.12276/abstracten_US
dc.identifier.doi10.1111/plb.12276en_US
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