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Constitutive OsCIN1 Expression Reprograms Source–Sink Dynamics and Compromises Agronomic Traits in Rice

Authors
Nguyen, Cong DanhEom, Joon-SeobCho, Jung-IlChoi, Seok-HyunKwak, Jae UngEom, Seong-CheolPhan, Kieu Anh ThiLee, JuhoJeon, Jong-SeongLee, Sang-Kyu
Issue Date
Nov-2025
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
carbon partitioning; cell wall invertase; OsCIN1; rice; sink strength; yield
Citation
International Journal of Molecular Sciences, v.26, no.23
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
26
Number
23
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/81613
DOI
10.3390/ijms262311471
ISSN
1661-6596
1422-0067
Abstract
Cell wall invertases (CINs) establish sucrose gradients between source and sink tissues, essential for the allocation of photoassimilates. Rice possesses nine CIN genes, among which OsCIN1 and OsCIN2 have been reported as key regulators of sink strength. To test whether increasing CIN activity enhances grain yield, we generated OsCIN1 overexpression lines in rice driven by the CaMV 35S promoter. Subcellular localization analysis of OsCIN1–GFP confirmed its apoplastic localization. OsCIN1 promoter::GUS analyses verified expression in vascular tissues and revealed predominant signals in the ovular vascular and lateral stylar vascular traces during seed development. Although CIN activity was markedly elevated throughout the plant, the resulting phenotypes were unexpected. Sugar profiling of flag leaves at the flowering stage showed almost complete sucrose depletion in the overexpression (OX) lines, accompanied by increased hexose and starch accumulation. Under field conditions, OsCIN1 OX plants exhibited ~50% fewer tillers and a lower 1000-grain weight relative to wild type (WT), resulting in reduced productivity. Ectopic expression of OsCIN1 disrupted the sucrose concentration gradient, weakened carbon partitioning to sink tissues, and impaired key agronomic traits. Collectively, sugar flux is governed by the spatiotemporal patterning of CINs, highlighting that precise spatial and temporal control of CIN activity is required to increase yield.
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