Research Group
WU Ligang

Email:  lgwu@@sibcb.ac.cn
Tel:  54921321
His/Her Lab

Education Background & Academic Experience
2008-present:  Principle Investigator, Shanghai Institute of Biochemistry and Cell Biology (SIBCB), CAS, Shanghai, China.

2001-2008:  Postdoctoral Fellow, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY, USA.  

1996-2001:   Ph.D. in Genetics, National Laboratory of Plant Molecular and Genetics, Shanghai Institute of Plant Physiology, The Chinese Academy of Sciences, Shanghai, China.

1992-1996:   B.S. in Biochemistry Engineering, Department of Bioscience and Technology, Shanghai Jiao Tong University, Shanghai, China.

Research Interests
The cells of various eukaryotic organisms contain numerous small and long non-coding RNAs (ncRNA). However, to the majority of those ncRNAs, the questions as basic as whether they have functions and their regulatory mechanisms are still mysterious.  Our previous studies have shown that microRNA (miRNA) destabilize messages to which they are partially complementary by expediting poly(A) tail removal, and further identified CAF1 as the nuclease responsible for mRNA deadenylation mediated by miRNA and off-target RNAi caused by partially complementary siRNA. More recently, we revealed a new function of miRNA in the cells that miRNAs can serve as a surveillance system to repress nonsense mRNAs by recognizing miRNA-responsive elements in the open reading frame region downstream of the premature termination codon. We will continue to focus on discovering novel functions of ncRNAs and elucidating their molecular mechanisms in cell fate determination, which will allow us to develop advanced technology to manipulate gene expression for both basic research and therapeutic applications. The current projects in this laboratory including:
1) Studying mechanism of small non-coding RNA in gene regulation.
2) Developing new strategy to improve the efficiency and specificity of RNAi and CRISPR.
3) Using high-throughput screening method to identify the function of small and long non-coding RNA in cell fate determination and uncover the molecular mechanism.


Publication (*Corresponding author)
1. Shang R, Zhang F, Xu B, Xi H, Zhang X, Wang W, and Wu L*. Ribozyme-enhanced single-stranded Ago2-processed interfering RNA triggers efficient gene silencing with fewer off-target effects. Nat Commun. (2015) 6:8430. DOI: 10.1038/ncomms9430
2. Liu S, Zhang X, Shi C, Lin J, Chen G, Wu B, Wu L, Shi H, Yuan Y, Zhou W, Sun Z, Dong X, Wang J. Altered microRNAs expression profiling in cumulus cells from patients with polycystic ovary syndrome. J Transl Med. (2015) 13:238. doi: 10.1186/s12967-015-0605-y.
3. Chen T, Hao Y, Zhang Y, Li M, Wang M, Han W, Wu Y, Lv Y, Hao J, Wang L, Li A, Yang Y, Jin K, Zhao X, Li Y, Ping X, Lai W, Wu L, Jiang G, Wang H, Sang L, Wang X, Yang Y, Zhou Q. m(6)A RNA methylation is regulated by microRNAs and promotes reprogramming to pluripotency. Cell Stem Cell. (2015) 16(3):289-301.
4. Wu Y, Zhou H, Fan X, Zhang Y, Zhang M, Wang Y, Xie Z, Bai M, Yin Q, Liang D, Tang W, Liao J, Zhou C, Liu W, Zhu P, Guo H, Pan H, Wu C, Shi H, Wu L*, Tang F*, Li J*. Correction of a Genetic Disease by CRISPR-Cas9-Mediated Gene Editing in Mouse Spermatogonial Stem Cells.  Cell research. (2015) 25 (1):67-79. 
5. Zhao Y, Lin J, Xu B, Hu S, Zhang X, and Wu L*. MicroRNA-mediated repression of nonsense mRNAs. Elife. (2014) Aug 8;3:e03032.   
Insight: “Stop the nonsense!”  Elife. (2014) 3:e04300
6. Gou L, Dai P, Yang J, Xue Y, Hu Y, Zhou Y, Kang J, Wang X, Li H, Hua M, Zhao S, Hu S, Wu L, Shi H, Li Y, Fu X, Qu L, Wang E, Liu M. Pachytene piRNAs instruct massive mRNA elimination during late spermiogenesis. Cell research. (2014) 24: 680–700.
7. Piao X, Zhang X, Wu L* and Belasco JG*. CCR4-NOT deadenylates mRNA associated with RNA-induced silencing complexes in human cells. Mol Cell Biol. (2010) 30(6): 1486-1494.
8. Savas JN, Ma B, Deinhardt K, Culver BP, Restituito S, Wu L, Belasco JG, Chao MV, and Tanese N. A role for huntington disease protein in dendritic RNA granules. J Biol Chem. (2010) 285(17): 13142-13153.
9. Wu L, Fan J, and Belasco JG. Importance of translation and nonnucleolytic ago proteins for on-target RNA interference. Curr Biol. (2008) 18(17): 1327-1332.
10. Wu L, and Belasco JG. Examining the influence of microRNAs on translation efficiency and on mRNA deadenylation and decay. Methods Enzymol. (2008) 449: 373-393.
11. Wu L, and Belasco JG. Let me count the ways: mechanisms of gene regulation by miRNAs and siRNAs. Mol Cell. (2008) 29(1): 1-7. (Invited Review)
12. Bao L, Zhou M, Wu L, Lu L, Goldowitz D, Williams RW, and Cui Y. PolymiRTS Database: linking polymorphisms in microRNA target sites with complex traits. Nucleic Acids Res. (2007) 35(Database issue): D51-54.
13. Wu L, Fan J, and Belasco JG. MicroRNAs direct rapid deadenylation of mRNA. Proc Natl Acad Sci U S A. (2006) 103(11): 4034-4039. 
Commentary: “MicroRNAs: new players in an old game.”, PNAS. (2006) 103(11):3951-2.
Research Highlights: “Behind the scenes”  Nature Review Genetics, Nature Review Molecular Biology, (2006) 243(7).
14. Wu L, and Belasco JG. Micro-RNA regulation of the mammalian lin-28 gene during neuronal differentiation of embryonal carcinoma cells. Mol Cell Biol. (2005) 25(21): 9198-9208.
15. Wu L, Fan J, Jiang L, Wang H, Song R, Zhang Q, Zhu H, Li N, Liu Z, and Xu Z. A specific cis-hairpin ribozyme facilitates infection of a TMV-based DNA vector in tobacco protoplasts. J Virol Methods. (2003) 111(2): 101-109.
16. Wu L, Jiang L, Zhou Z, Fan J, Zhang Q, Zhu H, Han Q, and Xu Z. Expression of foot-and-mouth disease virus epitopes in tobacco by a tobacco mosaic virus-based vector. Vaccine. (2003) 21(27-30): 4390-4398.
 

Team
333 Haike Road, Pudong District,
201210, Shanghai, P.R.China
Tel: 021-20778500
Email: ncpss@sibcb-ncpss.org