Yongzhen Wu

Dr. Yongzhen Wu

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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28 April 2015 in Plant Biotechnology Journal
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Journal Article
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YWYongzhen Wu
Yongzhen Wu
YFYongcai Fu
Yongcai Fu
SZShuangshuang Zhao
Shuangshuang Zhao
PGPing Gu
Ping Gu
ZZZuofeng Zhu
Zuofeng Zhu
LTLubin Tan
Lubin Tan

8 October 2018 in Nature Communications
Verified
Journal Article
Open access
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YWYongzhen Wu
Yongzhen Wu
SZShuangshuang Zhao
Shuangshuang Zhao
XLXianran Li
Xianran Li
BZBosen Zhang
Bosen Zhang
JLJiang Liyun
Jiang Liyun
LTLubin Tan
Lubin Tan
Improving the yield by modifying plant architecture was a key step during crop domestication. Here, we show that a 110-kb deletion on the short arm of chromosome 7 in Asian cultivated rice (Oryza sativa), which is closely linked to the previously identified PROSTRATE GROWTH 1 (PROG1) gene, harbors a tandem repeat of seven zinc-finger genes. Three of these genes regulate the plant architecture, suggesting that the deletion also promoted the critical transition from the prostrate growth and low yield of wild rice (O. rufipogon) to the erect growth and high yield of Asian cultivated rice. We refer to this locus as RICE PLANT ARCHITECTURE DOMESTICATION (RPAD). Further, a similar but independent 113-kb deletion is detected at the RPAD locus in African cultivated rice. These results indicate that the deletions, eliminating a tandem repeat of zinc-finger genes, may have been involved in the parallel domestication of plant architecture in Asian and African rice.

23 November 2016 in Journal of Integrative Plant Biology
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Journal Article
Closed access
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SZShuangshuang Zhao
Shuangshuang Zhao
LZLei Zhao
Lei Zhao
FLFengxia Liu
Fengxia Liu
YWYongzhen Wu
Yongzhen Wu
ZZZuofeng Zhu
Zuofeng Zhu
LTLubin Tan
Lubin Tan

6 July 2022 in Theoretical and Applied Genetics
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HXHuiyuan Xu
Huiyuan Xu
HSHan Sun
Han Sun
JDJiajin Dong
Jiajin Dong
CMChengxue Ma
Chengxue Ma
JLJingxue Li
Jingxue Li
YWYongzhen Wu
Yongzhen Wu

31 July 2014 in New Phytologist
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Journal Article
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HSHan Sun
Han Sun
ZGZhiai Guo
Zhiai Guo
LGLifeng Gao
Lifeng Gao
GZGuangyao Zhao
Guangyao Zhao
WZWenping Zhang
Wenping Zhang
JJJizeng Jia
Jizeng Jia

4 August 2020 in The Plant Journal
Verified
Journal Article
Open access
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XMXin Ma
Xin Ma
JFJinjian Fan
Jinjian Fan
YWYongzhen Wu
Yongzhen Wu
SZShuangshuang Zhao
Shuangshuang Zhao
XZXu Zheng
Xu Zheng
LTLubin Tan
Lubin Tan
SUMMARY: Asian cultivated rice (Oryza sativa) and African cultivated rice (Oryza glaberrima) originated from the wild rice species Oryza rufipogon and Oryza barthii, respectively. The genomes of both cultivated species have undergone profound changes during domestication. Whole‐genome de novo assemblies of O. barthii, O. glaberrima, O. rufipogon and Oryza nivara, produced using PacBio single‐molecule real‐time (SMRT) and next‐generation sequencing (NGS) technologies, showed that Gypsy‐like retrotransposons are the major contributors to genome size variation in African and Asian rice. Through the detection of genome‐wide structural variations (SVs), we observed that besides 28 shared SV hot spots, another 67 hot spots existed in either the Asian or African rice genomes. Based on gene annotation information of the SVs, we established that organelle‐to‐nucleus DNA transfers resulted in numerous SVs that participated in the nuclear genome divergence of rice species and subspecies. We detected 52 giant nuclear integrants of organelle DNA (NORGs, defined as >10 kb) in six Oryza AA genomes. In addition, we developed an effective method to genotype giant NORGs, based on genome assembly, and first showed the dynamic change in the distribution of giant NORGs in rice natural population. Interestingly, 16 highly differentiated giant NORGs tended to accumulate in natural populations of Asian rice from higher latitude regions, grown at lower temperatures and light intensities. Our study provides new insight into the genome divergence of African and Asian rice, and establishes that organelle‐to‐nucleus DNA transfers, as potentially powerful contributors to environmental adaptation during rice evolution, play a major role in producing SVs in rice genomes.