Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1763
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dc.contributor.authorBanerjee, Gopal-
dc.contributor.authorJonwal, Sarvesh-
dc.contributor.authorRengasamy, Balakrishnan-
dc.contributor.authorPal, Uttam-
dc.contributor.authorSingh, Dhanraj-
dc.contributor.authorMohit, Mohit-
dc.contributor.authorSinha, Alok Krishna-
dc.date.accessioned2025-10-15T05:41:39Z-
dc.date.available2025-10-15T05:41:39Z-
dc.date.issued2026-
dc.identifier.citationPlant Biotechnology Journal, 24(3): 1204-1222en_US
dc.identifier.issn1467-7644-
dc.identifier.issn1467-7652-
dc.identifier.otherhttps://doi.org/10.1111/pbi.70389-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/pbi.70389-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1763-
dc.descriptionAccepted date: 11 September 2025en_US
dc.description.abstractYield is a critical agronomic trait in cereal crops, shaped by factors like tiller and seed number, and seed weight. Understanding the factors governing these traits will help in improving the yield of plants. In this study, we identified an orphan gene, KRP3, belonging to cereal crops as a key regulator of rice plant architecture. Altered KRP3 protein homeostasis affected plant height, tiller number, and seed production, highlighting its role in maintaining rice plant vigor and productivity. The stability of the KRP3 protein is positively regulated by MPK3-mediated phosphorylation, as unphosphorylated KRP3 is targeted for degradation via the ubiquitin-proteasome pathway. Our findings reveal that the identified MPK3-KRP3 module operates as an S-phase checkpoint, modulating the pace of cell division in the actively dividing zones and maintaining a balance between cell division and elongation. These findings provide valuable insights for improving plant growth and grain yield in rice.en_US
dc.description.sponsorshipThe work is partially supported by the grant from the Department of Biotechnology, Government of India (Grant No.: BT/PR26207/GET/119/120/2017). G.B., U.P. and D.S. acknowledge the Council of Scientific and Industrial Research, Government of India, and BRIC-NIPGR for fellowship. S.J. acknowledges the Department of Biotechnology, Government of India for fellowship. A.K.S. thanks Sir JC Bose Fellowship from the Anusandhan National Research Foundation, Department of Science and Technology, Government of India (File no.: JCB/2020/000041). The work is partially supported by the grant from the Department of Biotechnology, Government of India (Grant No.: BT/PR26207/GET/119/120/2017). The authors also acknowledge the Gene Functional Analysis Platform for Crops, Confocal Facility, DNA sequencing facility, Radioisotope facility and the Central Instrumentation Facility of NIPGR, New Delhi, India.en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectKRP3en_US
dc.subjectMPK3en_US
dc.subjectcell cycleen_US
dc.subjectorphan geneen_US
dc.subjectproteasomeen_US
dc.subjectriceen_US
dc.subjectseed numberen_US
dc.subjecttilleren_US
dc.subjectubiquitinationen_US
dc.titleKRP3 stability controls rice plant architecture and productivity via MPK3-mediated phosphorylationen_US
dc.typeArticleen_US
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