Feizhen Wu

Feizhen Wu


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

View All Publications
1 September 2012 in Cell
Verified
Journal Article
Closed access
CLChristine Lian
Christine Lian
YXYufei Xu
Yufei Xu
CCCraig Ceol
Craig Ceol
FWFeizhen Wu
Feizhen Wu
ALAllison Larson
Allison Larson
YSYujiang Shi
Yujiang Shi

1 May 2011 in Molecular Cell
Verified
Journal Article
Closed access
YXYufei Xu
Yufei Xu
FWFeizhen Wu
Feizhen Wu
LTLi Tan
Li Tan
LKLingchun Kong
Lingchun Kong
LXLijun Xiong
Lijun Xiong
YSYujiang Shi
Yujiang Shi

1 February 2019 in Nature Protocols
Verified
Journal Article
Closed access
PDF file
BWBinbin Wang
Binbin Wang
MWMei Wang
Mei Wang
WZWubing Zhang
Wubing Zhang
TXTengfei Xiao
Tengfei Xiao
CCChen-Hao Chen
Chen-Hao Chen
XLX. Shirley Liu
X. Shirley Liu

18 July 2018 in Nature
Verified
Journal Article
Closed access
PDF file
DWDi Wu
Di Wu
DHDi Hu
Di Hu
HCHao Chen
Hao Chen
GSGuoming Shi
Guoming Shi
IFIrfete S. Fetahu
Irfete S. Fetahu
YSYujiang Shi
Yujiang Shi

27 January 2021 in Nature
Verified
Journal Article
Closed access
PDF file
WXWenqi Xu
Wenqi Xu
JLJiahui Li
Jiahui Li
CHChenxi He
Chenxi He
JWJing Wen
Jing Wen
HMHonghui Ma
Honghui Ma
HSHongjie Shen
Hongjie Shen

30 May 2017 in RNA Biology
Verified
Journal Article
Open access
MXMin Xiao
Min Xiao
JLJin Li
Jin Li
WLWei Li
Wei Li
YWYu Wang
Yu Wang
FWFeizhen Wu
Feizhen Wu
WYWenqiang Yu
Wenqiang Yu
MicroRNAs (miRNAs) are small non-coding RNAs that function as negative gene expression regulators. Emerging evidence shows that, except for function in the cytoplasm, miRNAs are also present in the nucleus. However, the functional significance of nuclear miRNAs remains largely undetermined. By screening miRNA database, we have identified a subset of miRNA that functions as enhancer regulators. Here, we found a set of miRNAs show gene-activation function. We focused on miR-24-1 and found that this miRNA unconventionally activates gene transcription by targeting enhancers. Consistently, the activation was completely abolished when the enhancer sequence was deleted by TALEN. Furthermore, we found that miR-24-1 activates enhancer RNA (eRNA) expression, alters histone modification, and increases the enrichment of p300 and RNA Pol II at the enhancer locus. Our results demonstrate a novel mechanism of miRNA as an enhancer trigger.