Yangyang Sun

Dr. Yangyang Sun

Hainan University, Haikou, Hainan, China
+1
orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 July 2018 in Plant Physiology
Verified
Journal Article
Open access
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YZYuanyuan Zhang
Yuanyuan Zhang
KCKai Chen
Kai Chen
FZFang-Jie Zhao
Fang-Jie Zhao
CSCuiju Sun
Cuiju Sun
Cheng JinCheng Jin
Cheng Jin
XLXingming Lian
Xingming Lian
Copper (Cu) is an essential micronutrient for plant growth. However, the molecular mechanisms underlying Cu trafficking and distribution to different organs in rice (Oryza sativa) are poorly understood. Here, we report the function and role of Antioxidant Protein1 (OsATX1), a Cu chaperone in rice. Knocking out OsATX1 resulted in increased Cu concentrations in roots, whereas OsATX1 overexpression reduced root Cu concentrations but increased Cu accumulation in the shoots. At the reproductive stage, the concentrations of Cu in developing tissues, including panicles, upper nodes and internodes, younger leaf blades, and leaf sheaths of the main tiller, were increased significantly in OsATX1-overexpressing plants and decreased in osatx1 mutants compared with the wild type. The osatx1 mutants also showed a higher Cu concentration in older leaves. Yeast two-hybrid and bimolecular fluorescence complementation assays showed that OsATX1 interacts with the rice heavy metal P1B-ATPases HMA4, HMA5, HMA6, and HMA9. These results suggest that OsATX1 may function to deliver Cu to heavy metal P1B-ATPases for Cu trafficking and distribution in order to maintain Cu homeostasis in different rice tissues. In addition, heterologous expression of OsATX1 in the yeast (Saccharomyces cerevisiae) cadmium-sensitive mutant Δycf1 increased the tolerance to Cu and cadmium by decreasing their respective concentrations in the transformed yeast cells. Taken together, our results indicate that OsATX1 plays an important role in facilitating root-to-shoot Cu translocation and the redistribution of Cu from old leaves to developing tissues and seeds in rice.

7 December 2020 in Nature Plants
Verified
Journal Article
Closed access
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CZChuansong Zhan
Chuansong Zhan
LLLong Lei
Long Lei
ZLZixin Liu
Zixin Liu
SZShen Zhou
Shen Zhou
CYChenkun Yang
Chenkun Yang
JLJie Luo
Jie Luo

23 January 2024 in New Phytologist
Verified
Journal Article
Open access
Yangyang SunYangyang Sun
Yangyang Sun
YZYutong Zhou
Yutong Zhou
QLQiyuan Long
Qiyuan Long
JXJunwei Xing
Junwei Xing
PGPeizhen Guo
Peizhen Guo
Cheng JinCheng Jin
Cheng Jin
Summary: Salt stress negatively affects rice growth, development and yield. Metabolic adjustments contribute to the adaptation of rice under salt stress. Branched‐chain amino acids (BCAA) are three essential amino acids that cannot be synthesized by humans or animals. However, little is known about the role of BCAA in response to salt stress in plants. Here, we showed that BCAAs may function as scavengers of reactive oxygen species (ROS) to provide protection against damage caused by salinity. We determined that branched‐chain aminotransferase 2 (OsBCAT2), a protein responsible for the degradation of BCAA, positively regulates salt tolerance. Salt significantly induces the expression of OsBCAT2 rather than BCAA synthesis genes, which indicated that salt mainly promotes BCAA degradation and not de novo synthesis. Metabolomics analysis revealed that vitamin B5 (VB5) biosynthesis pathway intermediates were higher in the OsBCAT2‐overexpressing plants but lower in osbcat2 mutants under salt stress. The salt stress‐sensitive phenotypes of the osbcat2 mutants are rescued by exogenous VB5, indicating that OsBCAT2 affects rice salt tolerance by regulating VB5 synthesis. Our work provides new insights into the enzymes involved in BCAAs degradation and VB5 biosynthesis and sheds light on the molecular mechanism of BCAAs in response to salt stress.

11 July 2020 in New Phytologist
Verified
Journal Article
Closed access
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Yangyang SunYangyang Sun
Yangyang Sun
YSYuheng Shi
Yuheng Shi
GLGuige Liu
Guige Liu
FYFang Yao
Fang Yao
YZYuanyuan Zhang
Yuanyuan Zhang
JLJie Luo
Jie Luo

Verified
Journal Article
Open access
PDF file
Yangyang SunYangyang Sun
Yangyang Sun
BWBi Wang
Bi Wang
JRJunxia Ren
Junxia Ren
YZYutong Zhou
Yutong Zhou
YHYu Han
Yu Han
JLJie Luo
Jie Luo
Serotonin (5-hydroxytryptamine) plays an important role in many developmental processes and biotic/abiotic stress responses in plants. Although serotonin biosynthetic pathways in plants have been uncovered, knowledge of the mechanisms of serotonin accumulation is still limited, and no regulators have been identified to date. Here, we identified the basic leucine zipper transcription factor OsbZIP18 as a positive regulator of serotonin biosynthesis in rice. Overexpression of OsbZIP18 strongly induced the levels of serotonin and its early precursors (tryptophan and tryptamine), resulting in stunted growth and dark-brown phenotypes. A function analysis showed that OsbZIP18 activated serotonin biosynthesis genes (including tryptophan decarboxylase 1 (OsTDC1), tryptophan decarboxylase 3 (OsTDC3), and tryptamine 5-hydroxylase (OsT5H)) by directly binding to the ACE-containing or G-box cis-elements in their promoters. Furthermore, we demonstrated that OsbZIP18 is induced by UV-B stress, and experiments using UV-B radiation showed that transgenic plants overexpressing OsbZIP18 exhibited UV-B stress-sensitive phenotypes. Besides, exogenous serotonin significantly exacerbates UV-B stress of OsbZIP18_OE plants, suggesting that the excessive accumulation of serotonin may be responsible for the sensitivity of OsbZIP18_OE plants to UV-B stress. Overall, we identified a positive regulator of serotonin biosynthesis and demonstrated that UV-B-stress induced serotonin accumulation, partly in an OsbZIP18-dependent manner.

15 June 2023 in International Immunopharmacology
Verified
Journal Article
Closed access
YZYonghuan Zhang
Yonghuan Zhang
Yangyang SunYangyang Sun
Yangyang Sun
YHYing Hu
Ying Hu
SZShaowen Zheng
Shaowen Zheng
HSHaigang Shao
Haigang Shao
CLChen li
Chen li