Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1735
Title: The rice heat shock transcription factor OsHSFC1b increases seed weight, size, and vigor, but its function is disrupted by isoaspartyl modification
Authors: Achary, Rakesh Kumar
Kamble, Nitin Uttam
Gautam, Shikha
Hazra, Abhijit
Varshney, Vishal
Mahawar, Shivangi
Laha, Saroj
Majee, Manoj
Keywords: Oryza sativa
seed vigor
eed weight
eed size
HSFC1b
Protein-repairing enzymes (PRE)
PIMT
isoaspartate (isoAsp)
Issue Date: 2025
Publisher: John Wiley & Sons
Citation: Plant Journal, 123(2): e70365
Abstract: Plant optimizes seed size, weight, vigor, and various other features during seed development, which are important not only for their successful propagation and establishment but also for effective agriculture. Despite several studies conducted, understanding how plants coordinate the regulatory mechanisms to achieve optimal seed size, weight, and vigor remains elusive. Here, our study reveals the role of rice heat shock transcription factor OsHSFC1b in modulating various seed attributes. We observe that OsHSFC1b expression increases during the later stage of seed development and is primarily localized in the embryo. We found that hsfc1b genome-edited lines exhibit compromised seed size, weight, and vigor, while overexpression lines exhibit increased seed size, weight, and vigor compared with the wild-type seeds. Our study further reveals that OsHSFC1b improves seed vigor by activating HSPs and RFO biosynthetic genes involved in protection mechanisms, while also mediating seed size and weight by modulating auxin biosynthesis, endosperm development, and seed filling. We found that upon ageing and stressful environments, OsHSFC1b undergoes isoaspartyl modification that negatively impacts its biological function in seeds. Our MS/MS analyses confirm that asparagine residues near the DNA-binding domain and nuclear localization sequence of OsHSFC1b undergo isoaspartyl modification that adversely affects OsHSFC1b's transactivation activity. However, PROTEIN L-ISOASPARTYL METHYLTRANSFERASE interacts and repairs this isoaspartate-mediated damage, and restores the function of OsHSFC1b. Taken together, our study uncovers how isoaspartyl modification affects the transactivation ability of OsHSFC1b, yet the intervention of PIMT not only repairs this damage but also elevates agronomically important seed traits.
Description: Accepted date: 10 July 2025
URI: https://onlinelibrary.wiley.com/doi/10.1111/tpj.70365
http://223.31.159.10:8080/jspui/handle/123456789/1735
ISSN: 0960-7412
1365-313X
Appears in Collections:Institutional Publications

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