Yunwei Zhou

Yunwei Zhou


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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1 March 2018 in Plant Physiology and Biochemistry
Verified
Journal Article
Closed access
WGWenjie Gao
Wenjie Gao
MHMiao He
Miao He
JLJie Liu
Jie Liu
XMXin Ma
Xin Ma
YZYu Zhang
Yu Zhang
YZYunwei Zhou
Yunwei Zhou

11 November 2022 in Plant Growth Regulation
Verified
Journal Article
Closed access
PDF file
WGWenjie Gao
Wenjie Gao
QMQingran Meng
Qingran Meng
XWXiang Wang
Xiang Wang
FCFeng Chen
Feng Chen
MHMiao He
Miao He
YZYunwei Zhou
Yunwei Zhou

1 December 2022 in Journal of Plant Growth Regulation
Verified
Journal Article
Closed access
PDF file
WGWenjie Gao
Wenjie Gao
QMQingran Meng
Qingran Meng
XWXiang Wang
Xiang Wang
FCFeng Chen
Feng Chen
YZYunwei Zhou
Yunwei Zhou
MHMiao He
Miao He

21 December 2022 in Frontiers in Plant Science
Verified
Journal Article
Open access
LCLifei Chen
Lifei Chen
BXBin Xia
Bin Xia
ZLZiwei Li
Ziwei Li
XLXiaowei Liu
Xiaowei Liu
YBYun Bai
Yun Bai
YZYunwei Zhou
Yunwei Zhou
Syringa oblata is a high ornamental value tree owing to its elegant colors, unique aromas and wide adaptability, however, studies on the molecular mechanism underlying the formation of its ornamental traits are still lacking. Here, we presented a chromosome-scale genome assembly of S. oblata and the final genome size was 1.11 Gb with a contig N50 of 4.75 Mb, anchored on 23 chromosomes and was a better reference for S. oblata transcriptome assembly. Further by integrating transcriptomic and metabolic data, it was concluded that F3H, F3’H, 4CL and PAL, especially the F3’H, were important candidates involved in the formation of floral color differences among S. oblata individuals. Genome-wide identification and analysis revealed that the TPS-b subfamily was the most abundant subfamily of TPS family in S. oblata, which together with the CYP76 family genes determined the formation of the major floral volatiles of S. oblata. Overall, our results provide an important reference for mechanistic studies on the main ornamental traits and molecular breeding in S. oblata.

21 April 2022 in Research Square
Verified
Preprint
Open access
PDF file
WGWenjie Gao
Wenjie Gao
QMQingran Meng
Qingran Meng
XWXiang Wang
Xiang Wang
FCFeng Chen
Feng Chen
MHMiao He
Miao He
YZYunwei Zhou
Yunwei Zhou
Geranyl diphosphate synthase (GPS) and farnesyl diphosphate synthase (FPS) catalyzes the biosynthesis of monoterpenoids and sesquiterpenoids, two key precursors for terpenoids biosynthesis. Here, the open reading frame (ORF) sequences of GPS (named CiGPS) and FPS (named CiFPS) with lengths of 1278 bp and 1035 bp were cloned from Chrysanthemum indicum var. aromaticum (C. indicum var. aromaticum). Phylogenetic analysis showed that CiGPS and CiFPS genes were closely related to Artemisia annua and Chrysanthemum × morifolium, respectively. qRT-PCR results showed that CiGPS and CiFPS gene had the highest expression level in leaves, while the expression of CiFPS was induced to methyl jasmonate. Overexpression of CiGPS and CiFPS in tobacco resulted in shorter plant height, darker leaf color, higher chlorophyll, and carotenoid content; the number of long handle trichomes increased significantly, while short handle trichomes only increased significantly on the upper epidermis of leaves of CiGPS transgenic tobacco lines. The relative content of terpenes of CiGPS and CiFPS transgenic tobacco lines increased significantly and monoterpenoids and sesquiterpenoids were detected in transgenic tobacco without wild type (WT) and empty vector (EV) lines. The activity of GPS enzyme was increased in CiGPS transgenic tobacco lines, but FPS enzyme activity in CiFPS transgenic tobacco lines was non-significant. Transcriptional analyses revealed that the expression levels of terpenoid biosynthesis pathway genes were higher in transgenic tobacco lines than in WT and EV lines. All the results demonstrated that GPS and FPS cDNA were effective to improve growth traits and alter terpenoid metabolism of C. indicum var. aromaticum.