Lin Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Lin Wang has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Changxian Yang
National Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, Huazhong Agriculture University, No. 1 Shizishan Street, Hongshan District, Wuhan 430070, China
1 shared publication - Chunmei Shi
Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences in Weifang, No. 699 Binhu Road, Xiashan Eco-Economic Development Zone, Weifang 261325, China
1 shared publication - Liepeng Dong
Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences in Weifang, No. 699 Binhu Road, Xiashan Eco-Economic Development Zone, Weifang 261325, China
1 shared publication - Qingmin Xie
College of Horticulture and Landscape Architecture, Yangzhou University, Yangzhou 225009, China
1 shared publication - Sidratul Muntha
Peking University Institute of Advanced Agricultural Sciences, Shandong Laboratory of Advanced Agricultural Sciences in Weifang, No. 699 Binhu Road, Xiashan Eco-Economic Development Zone, Weifang 261325, China
1 shared publication - Taotao Wang
National Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, Huazhong Agricultural University , Wuhan 430070
1 shared publication
Latest Publications
- Open Access
- 26 January 2026
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (3) , 1227
A Noncanonical Auxin-Sensing Mechanism Uncovered by Screening the Auxin Response Factor 3 Interacting Proteins in Tomato
Within the canonical auxin signaling pathway, Auxin Response Factors (ARFs) are transcriptionally repressed by AUX/IAA proteins under low auxin conditions, and this repression is alleviated as auxin concentrations increase. By contrast, ARF3 functions as a central regulator of gynoecium morphogenesis in Arabidopsis via a non-canonical auxin-sensing mechanism that relies on dose-dependent modulation of its protein–protein interaction network. To investigate whether an analogous regulatory mechanism operates in tomato (Solanum lycopersicum), we identified the tomato ARF3 homolog (SlARF3) and utilized it as bait in a yeast two-hybrid (Y2H) screen. This screening approach yielded 137 positive clones, corresponding to 118 putative interacting proteins. Notably, all of these interactions were abolished in the presence of 3-indoleacetic acid (IAA), indicating that SlARF3 engages in auxin-sensitive protein–protein interactions and thereby mediates auxin-dependent signal transduction. Among these, we identified an auxin-sensitive interaction between SlARF3 and TM29, a central regulator of parthenocarpy, underscoring its critical role in this developmental pathway. Functional analyses further demonstrated that silencing SlARF3 induces parthenocarpic fruit formation. Taken together, these findings define a previously uncharacterized SlARF3-centered interaction network and provide a conceptual framework for elucidating non-canonical auxin signaling pathways underlying tomato development.
- 26 January 2026
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (3) , 1227
Open AccessA Noncanonical Auxin-Sensing Mechanism Uncovered by Screening the Auxin Response Factor 3 Interacting Proteins in Tomato
Within the canonical auxin signaling pathway, Auxin Response Factors (ARFs) are transcriptionally repressed by AUX/IAA proteins under low auxin conditions, and this repression is alleviated as auxin concentrations increase. By contrast, ARF3 functions as a central regulator of gynoecium morphogenesis in Arabidopsis via a non-canonical auxin-sensing mechanism that relies on dose-dependent modulation of its protein–protein interaction network. To investigate whether an analogous regulatory mechanism operates in tomato (Solanum lycopersicum), we identified the tomato ARF3 homolog (SlARF3) and utilized it as bait in a yeast two-hybrid (Y2H) screen. This screening approach yielded 137 positive clones, corresponding to 118 putative interacting proteins. Notably, all of these interactions were abolished in the presence of 3-indoleacetic acid (IAA), indicating that SlARF3 engages in auxin-sensitive protein–protein interactions and thereby mediates auxin-dependent signal transduction. Among these, we identified an auxin-sensitive interaction between SlARF3 and TM29, a central regulator of parthenocarpy, underscoring its critical role in this developmental pathway. Functional analyses further demonstrated that silencing SlARF3 induces parthenocarpic fruit formation. Taken together, these findings define a previously uncharacterized SlARF3-centered interaction network and provide a conceptual framework for elucidating non-canonical auxin signaling pathways underlying tomato development.