Analysis of rice proteins with DLN repressor Motif/S

dc.contributor.authorSingh, Purnima
dc.contributor.authorMathew, Iny Elizebeth
dc.contributor.authorVerma, Ankit
dc.contributor.authorTyagi, Akhilesh K.
dc.contributor.authorAgarwal, Pinky
dc.date.accessioned2019-04-03T07:44:28Z
dc.date.available2019-04-03T07:44:28Z
dc.date.issued2019
dc.descriptionAccepted date: 31 January 2019en_US
dc.description.abstractTranscriptional regulation includes both activation and repression of downstream genes. In plants, a well-established class of repressors are proteins with an ERF-associated amphiphilic repression/EAR domain. They contain either DLNxxP or LxLxL as the identifying hexapeptide motif. In rice (Oryza sativa), we have identified a total of 266 DLN repressor proteins, with the former motif and its modifications thereof comprising 227 transcription factors and 39 transcriptional regulators. Apart from DLNxxP motif conservation, DLNxP and DLNxxxP motifs with variable numbers/positions of proline and those without any proline conservation have been identified. Most of the DLN repressome proteins have a single DLN motif, with higher relative percentage in the C-terminal region. We have designed a simple yeast-based experiment wherein a DLN motif can successfully cause strong repression of downstream reporter genes, when fused to a transcriptional activator of rice or yeast. The DLN hexapeptide motif is essential for repression, and at least two “DLN” residues cause maximal repression. Comparatively, rice has more DLN repressor encoding genes than Arabidopsis, and DLNSPP motif from rice is 40% stronger than the known Arabidopsis SRDX motif. The study reports a straightforward assay to analyze repressor activity, along with the identification of a strong DLN repressor from rice.en_US
dc.description.sponsorshipI.E.M. and A.V. acknowledge the junior and senior research fellowships from University Grants Commission, India and Department of Biotechnology, India, respectively. P.S., A.K.T., and P.A. acknowledge the research grants from the Department of Biotechnology, India. P.A. is thankful for the core grant from NIPGR.en_US
dc.identifier.citationInternational Journal of Molecular Sciences, 20(7): 1600en_US
dc.identifier.doi10.3390/ijms20071600en_US
dc.identifier.issn1422-0067
dc.identifier.officialurlhttps://www.mdpi.com/1422-0067/20/7/1600/htmen_US
dc.identifier.urihttps://ndkr-library.nipgr.ac.in/handle/123456789/937
dc.language.isoen_USen_US
dc.publisherMDPI AGen_US
dc.subjectEAR motifen_US
dc.subjectriceen_US
dc.subjectseed developmenten_US
dc.subjecttrans-repressionen_US
dc.subjectyeasten_US
dc.titleAnalysis of rice proteins with DLN repressor Motif/Sen_US
dc.typeArticleen_US

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