Zefeng Wang

Zefeng Wang

Associate Professor

Department of Pharmacology

Ph.D., Biological Chemistry
Johns Hopkins University, Baltimore MD

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Wang Website

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Research Interests

  • Regulation code for alternative splicing
  • Function of splicing factors in human cancer
  • Bioengineering of artificial factors to manipulate control RNA splicing and stability

Research Synopsis

My lab currently works on two main areas of RNA biology. Our main focus is to study how alternative splicing is regulated in a systematic level and how such regulation responds to cellular signaling pathways during key biological processes. In addition, we developed new approaches to manipulate splicing and other RNA processing pathways by engineering artificial factors that specifically recognize a given RNA target.  In summary, my lab is seeking to solve the “splicing code” (i.e. a set of rules for splicing regulation by cis-elements and trans-factors) and to reprogram the code to control gene function.  Since alternative splicing is a key regulatory mode for the majority of human genes and the splicing dysregulation is a common cause of various diseases, our research can provide important insight to fundamental biology and human diseases.

1. Systematic study of splicing regulatory elements and factors

We use new cell-based screen systems to unbiasedly identify intronic splicing enhancers and silencers (ISE and ISS) from random sequences. These elements are further used as baits to identify putative trans-acting splicing factors.  Our results suggested a complex, overlapping network of protein-RNA interactions between ISS or ISE motifs and their trans-factors. This arrangement may enable individual cis-element to exert different regulatory functions in distinct cellular contexts depending on the spectrum of regulatory factors present.

2. Splicing regulation in cancers

One of molecular hallmark for human cancer is dis-regulation of alternative splicing in many genes on a systematic scale. We identified several splicing factors that function as oncogenes or tumor suppressors.  One of such genes is DAZAP1 that function as a general splicing activator by to promote inclusion of weak exons through specific recognition of diverse cis-elements. The C-terminal proline-rich domain of DAZAP1 is phosphorylated by the MEK/Erk pathway, and is sufficient to activate splicing when recruited to pre-mRNA.  The phosphorylation by MEK/Erk is essential for the splicing regulatory activity and the nuclear/cytoplasmic translocation of DAZAP1. Knockdown or over-expression of DAZAP1 caused a cell proliferation defect that was independent of apoptosis. Taken together, these studies reveal a molecular mechanism that integrates the splicing control into MEK/Erk regulated cell proliferation and migration.  We found another splicing factor, RBM4, has tumor suppressor activity and involved in the regulation of cell apoptosis.  In addition, we found several splicing regulatory proteins can control DNA damage repair and cell cycle pathway though modulating alternative splicing, providing new links between RNA splicing and cancer.

3. Engineering artificial factors to modulate RNA splicing and stability

Another research area of my lab is to use the synthetic biology approach to engineer novel factors that specifically manipulate RNA metabolism.  My lab was the first to engineer “designer” splicing factors by combining sequence-specific RNA-binding domains of human Pumilio1 (PUF domains) with functional domains that promote or inhibit splicing. We applied these factors to modulate different types of alternative splicing in various targets including an anticancer target Bcl-X. Our work permitted the creation of artificial factors to target virtually any pre-mRNA, providing a strategy to study splicing regulation and to manipulate disease-associated splicing events.  Using a similar strategy, we engineered artificial site-specific RNA endonuclease by combining PUF domain with a general RNA endonuclease domain. The resulting enzyme is analogous to a “restriction enzyme” of RNA in that it can specifically recognize RNA and efficiently cleave near the binding site.  Since a PUF domain can be reprogrammed to bind any 8-nt sequence, our artificial enzymes provide a new gene tool that is very useful in studying the function of non-coding RNAs.

Publications

pubmed

Click above for PubMeb publications.

  • Wang Y, Xiao X, Zhang J, Choudhury R, Robertson A, Li K, Ma M, Burge CB and Wang Z.  (2013) A complex network of factors with overlapping affinities control splicing repression by intronic elements. Nature Structure Molecular Biology, 20(1):36-45. doi: 10.1038/nsmb.2459. Epub 2012 Dec 16. Abstract
  • Choudhury R, Dominguez D, Wang Y and Wang Z. Engineering RNA endonucleases with customized sequence specificities. (2012). Nature Communication, 3:1147. doi: 10.1038/ncomms2154. Abstract
  • Wang Y, Ma M, Xiao XS and Wang Z. (2012) Intronic splicing enhancers, cognate splicing factors and context dependent regulation rules. Nature Structure Molecular Biology, 19(10):1044-52. doi: 10.1038/nsmb.2377. Epub 2012 Sep 16. Abstract
  • Dong S, Wang Y, Cassidy-Amstutz C, Lu G, Bigler R, Li C, Jezyk MR, Hall TM , Wang Z. (2011) A specific and modular binding code for cytosine recognition in PUF domains. J Biol Chem., 286(30):26732-42. Epub 2011 Jun 8. *Selected as the paper of the week by J Bio. Chem,. *Recommended by an editorial comment in Chem Biol. 2011 Jul 29;18 (7):821-3. Abstract
  • Burd CE, Jeck WR, Liu Y, Sanoff HK, Wang Z, Sharpless NE. (2010) Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk. PloS Genet, 6(12):e1001233. Abstract
  • Wang Y, Cheong CG, Hall TM, Wang Z. (2009) Engineering splicing factors with designed specificities. Nature Methods, 6(11):825-30. Epub 2009 Oct 4. * Recommended by Faculty of 1000 * Commented by Science-Business eXchange. Abstract
  • Xiao X, Wang Z, Jang M, Nutiu R, Wang ET, Burge CB. (2009) Splice site strength-dependent activity and genetic buffering by poly-G runs. Nature Struct Mol Biol.,16(10):1094-100. Epub 2009 Sep 13. Abstract

Contact Information


Office Location:
4113 Genetic Medicine

Mailing Address:
CB # 7365
UNC-CH School of Medicine
Chapel Hill, NC 27599-7365

Office Phone: 919-966-0131
Fax: 919-966-5640
zefeng[at]med.unc.edu

 

 

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