Jiaqiang Sun

Dr. Jiaqiang Sun


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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25 February 2019 in New Phytologist
Verified
Journal Article
Closed access
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LJLan Ju
Lan Ju
YJYexing Jing
Yexing Jing
PSPengtao Shi
Pengtao Shi
JLJie Liu
Jie Liu
JCJiansheng Chen
Jiansheng Chen
JSJiaqiang Sun
Jiaqiang Sun

19 May 2017 in Plant Physiology
Verified
Journal Article
Open access
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JLJie Liu
Jie Liu
XCXiliu Cheng
Xiliu Cheng
PLPan Liu
Pan Liu
JSJiaqiang Sun
Jiaqiang Sun
MiR156-regulated SBP-box transcription factors function antagonistically with DWARF53 to regulate TEOSINTE BRANCHED1 and BARREN STALK1 expression during bread w

20 January 2021 in Journal of Experimental Botany
Verified
Journal Article
Open access
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LTLi Tai
Li Tai
HWHong-Jin Wang
Hong-Jin Wang
XXXiao-Jing Xu
Xiao-Jing Xu
WSWei-Hang Sun
Wei-Hang Sun
LJLan Ju
Lan Ju
KCKun-Ming Chen
Kun-Ming Chen
With the growth of the global population and the increasing frequency of natural disasters, crop yields must be steadily increased to enhance human adaptability to risks. Pre-harvest sprouting (PHS), a term mainly used to describe the phenomenon in which grains germinate on the mother plant directly before harvest, is a serious global problem for agricultural production. After domestication, the dormancy level of cultivated crops was generally lower than that of their wild ancestors. Although the shortened dormancy period likely improved the industrial performance of cereals such as wheat, barley, rice, and maize, the excessive germination rate has caused frequent PHS in areas with higher rainfall, resulting in great economic losses. Here, we systematically review the causes of PHS and its consequences, the major indicators and methods for PHS assessment, and emphasize the biological significance of PHS in crop production. Wheat quantitative trait loci functioning in the control of PHS are also comprehensively summarized in a meta-analysis. Finally, we use Arabidopsis as a model plant to develop more complete PHS regulatory networks for wheat. The integration of this information is conducive to the development of custom-made cultivated lines suitable for different demands and regions, and is of great significance for improving crop yields and economic benefits.

1 May 2019 in Molecular Plant
Verified
Journal Article
Closed access
GHGuanhua He
Guanhua He
JLJie Liu
Jie Liu
HDHuixue Dong
Huixue Dong
JSJiaqiang Sun
Jiaqiang Sun

30 July 2018 in Plant Physiology
Verified
Journal Article
Open access
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XCXiliu Cheng
Xiliu Cheng
SZShaoxuan Zhang
Shaoxuan Zhang
WTWeichun Tao
Weichun Tao
XZXiangxiang Zhang
Xiangxiang Zhang
JLJie Liu
Jie Liu
TCTao Chen
Tao Chen
Perception and transduction of salt stress signals are critical for plant survival, growth, and propagation. Thus, identification of components of the salt stress-signaling pathway is important for rice (Oryza sativa) molecular breeding of salt stress resistance. Here, we report the identification of an apetala2/ethylene response factor transcription factor INDETERMINATE SPIKELET1 (IDS1) and its roles in the regulation of rice salt tolerance. By genetic screening and phenotype analysis, we demonstrated that IDS1 conferred transcriptional repression activity and acted as a negative regulator of salt tolerance in rice. To identify potential downstream target genes regulated by IDS1, we conducted chromatin immunoprecipitation (ChIP) sequencing and ChIP-quantitative PCR assays and found that IDS1 may directly associate with the GCC-box-containing motifs in the promoter regions of abiotic stress-responsive genes, including LEA1 (LATE EMBRYOGENESIS ABUNDANT PROTEIN1) and SOS1 (SALT OVERLY SENSITIVE1), which are key genes regulating rice salt tolerance. IDS1 physically interacted with the transcriptional corepressor topless-related 1 and the histone deacetylase HDA1, contributing to the repression of LEA1 and SOS1 expression. Analyses of histone H3 acetylation status and RNA polymerase II occupation on the promoters of LEA1 and SOS1 further defined the molecular foundation of the transcriptional repression activity of IDS1. Our findings illustrate an epigenetic mechanism by which IDS1 modulates salt stress signaling as well as salt tolerance in rice.

30 May 2017 in PLOS Genetics
Verified
Journal Article
Open access
PDF file
JLJie Liu
Jie Liu
XCXiliu Cheng
Xiliu Cheng
PLPan Liu
Pan Liu
DLDayong Li
Dayong Li
TCTao Chen
Tao Chen
JSJiaqiang Sun
Jiaqiang Sun
The transcription factor CONSTANS (CO) is a central component that promotes Arabidopsis flowering under long-day conditions (LDs). Here, we show that the microRNA319-regulated TEOSINTE BRANCHED/CYCLOIDEA/PCF (TCP) transcription factors promote photoperiodic flowering through binding to the CO promoter and activating its transcription. Meanwhile, these TCPs directly interact with the flowering activators FLOWERING BHLH (FBHs), but not the flowering repressors CYCLING DOF FACTORs (CDFs), to additively activate CO expression. Furthermore, both the TCPs and FBHs physically interact with the flowering time regulator PHYTOCHROME AND FLOWERING TIME 1 (PFT1) to facilitate CO transcription. Our findings provide evidence that a set of transcriptional activators act directly and additively at the CO promoter to promote CO transcription, and establish a molecular mechanism underlying the regulation of photoperiodic flowering time in Arabidopsis. Plants monitor day-length changes (photoperiod) throughout the year to precisely align their flowering time, which is crucial for successful reproduction. In Arabidopsis, some components, such as CONSTANS (CO), have been proved to play central roles in promoting the photoperiodic flowering under long-day conditions (LDs). In this study, we demonstrate that the microRNA319-regulated TEOSINTE BRANCHED/CYCLOIDEA/PCF (TCP) transcription factors directly bind to the CO promoter. Meanwhile, these TCPs physically interact with the flowering activators FLOWERING BHLH (FBHs) and the flowering regulator PHYTOCHROME AND FLOWERING TIME 1 (PFT1) to form a complex to activate CO transcription and promote photoperiodic flowering under LDs. Our results emphasize the importance of miR319-regulated TCPs in regulating plant flowering time.