Difference between revisions of "Test"

From Zhang Laboratory

Jump to: navigation, search
(Variation of RNA-regulatory networks in evolution, human populations and in neuronal disorders)
Line 1: Line 1:
__NOTOC__
+
{{#meta: keywords | computational biology; systems biology; RNA splicing and regulatory networks; gene expression }}{{#meta: description | The Chaolin Zhang Laboratory Home Page at Columbia University}}{{#meta: Content-Type | text/html; charset=utf-8 }}
  
 +
<html>
  
We are working on '''RNA''' at the interface of Systems Biology, Computer Science and Molecular Neuroscience, currently sponsored by NIH, Simons Foundation, and Columbia University Medical Center.
 
  
==Overview==
 
  
{|class="zebra wikitable" width="100%" style="border:0px solid; border-collapse:collapse;"
+
<script type="text/javascript" src="/data/Jssor/js/Jssor.Core.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.Debug.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.EventManager.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.Easing.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.Point.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.Utils.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.Navigator.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.CaptionSlider.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.Slider.js"></script>
 +
    <script type="text/javascript" src="/data/Jssor/js/Jssor.ThumbnailNavigator.js"></script>
 +
    <script>
 +
        jssor_slider1_starter = function (containerId) {
 +
            var _CaptionTransitions = [];
 +
            //Left to Right
 +
            _CaptionTransitions["L-R"] = { $Duration: 600, $FlyDirection: 1 };
 +
            //Right to Left
 +
            _CaptionTransitions["R-L"] = { $Duration: 600, $FlyDirection: 2 };
 +
            //Top to Bottom
 +
            _CaptionTransitions["T-B"] = { $Duration: 600, $FlyDirection: 4 };
 +
            //Bottom to Top
 +
            _CaptionTransitions["B-T"] = { $Duration: 600, $FlyDirection: 8 };
  
|-
+
            //To build caption transition code, reference to http://slideshow.jssor.com/documentation/transition-builder-caption.html
|
+
Post-transcriptional regulation at the RNA level has profound impact on gene expression, especial for the development and function of the nervous system. Such regulation is dictated by interaction of at least several hundred RNA-binding proteins (RBPs) with their target transcripts, or RNA-regulatory networks. Our current work focus on '''neuron-specific alternative splicing''', one critical step of RNA regulation.  Our research interests range from '''basic understanding of the specificity of protein-RNA interaction, to organization of splicing regulatory networks, and to function of specific splice variants'''.
+
  
 +
            var jssor_slider1 = new $JssorSlider$(containerId, {
 +
                //$SlideDuration:1200,
 +
                $HoverToPause: true,
 +
                $ShowLoading: true,                                //[Optional] Show loading screen or not default value is false
 +
                $AutoPlay: true,                                    //[Optional] Whether to auto play, default value is false
 +
                $PlayOrientation: 2,                                //[Optional] Orientation to play slide (for auto play, navigation), 1 horizental, 2 vertical, default value is 1
 +
                $DragOrientation: 3,                                //[Optional] Orientation to drag slide, 0 no drag, 1 horizental, 2 vertical, 3 either, default value is 1 (Note that the $DragOrientation should be the same as $PlayOrientation when $DisplayPieces is greater than 1, or parking position is not 0)
  
|
+
                $CaptionSliderOptions: {                            //[Optional] Options which specifies how to animate caption
[[File:splicing.png|right|300px]]
+
                    $Class: $JssorCaptionSlider$,                  //[Required] Class to create instance to animate caption
 +
                    $CaptionTransitions: _CaptionTransitions,      //[Required] Caption transitions to play caption, see caption transition section at jssor slideshow transition builder
 +
                    $PlayInMode: 1,                                //[Optional] 0 None (no play), 1 Chain (goes after main slide), 2 Parallel (goes synchronous with main slide), default value is 1
 +
                    $PlayOutMode: 1                                //[Optional] 0 None (no play), 1 Chain (goes before main slide), 2 Parallel (goes synchronous with main slide), default value is 1
 +
                }
 +
            });
 +
        }
 +
    </script>
  
|}
+
<center>
 +
    <div id="slider1_container" class="slider1" style="position: relative; width: 400px; height: 200px;">
 +
   
 +
        <!-- Loading Screen -->
 +
        <div u="loading" style="position: absolute; top: 0px; left: 0px;">
 +
            <div style="filter: alpha(opacity=70); opacity:0.7; position: absolute; display: block;
 +
                background-color: #000000; top: 0px; left: 0px;width: 100%;height:100%;">
 +
            </div>
 +
            <div style="position: absolute; display: block; background: url(/data/Jssor/img/loading.gif) no-repeat center center;
 +
                top: 0px; left: 0px;width: 100%;height:100%;">
 +
            </div>
 +
        </div>
  
 +
        <!-- Slides Container -->
 +
        <div u="slides" style="position: absolute; left: 0px; top: 0px; overflow: hidden;">
  
==Protein-RNA interactions at single nucleotide resolution==
+
            <div>
 +
                <a u=image href="/index.php/Research" rel="nofollow"><img u="image" src="/data/images/slideshow/as.png" width="386" height="300" /></a>
 +
            </div>
  
{|class="zebra wikitable" width="100%" style="border:0px solid; border-collapse:collapse;"
+
            <div>
 +
                <a u=image href="http://www.pnas.org/content/early/2015/03/02/1502849112.abstract" rel="nofollow"><img u="image" src="/data/images/slideshow/CortexAS.png" width="400" height="200" /></a>
 +
            </div>
  
|-
+
            <div>
|
+
                <a u=image href="https://sfari.org" rel="nofollow"><img u="image" src="/data/images/slideshow/SFARI2.png" width="400" height="200" /></a>
The RBP binding sites are notoriously difficult to map probably because of the flexibility of RNA.  The development of cross linking and immunoprecipitation followed by high-throughput sequencing (HITS-CLIP or CLIP-Seq) has been a revolution to the RNA field. This high-throughput biochemical assay makes it possible to map in vivo protein-RNA interactions on a genome wide scale.  Standard analysis pipelines of CLIP data typically map protein-RNA interaction sites at a resolution of ~30-60 nt. We developed a new computational method to determine the exact protein-RNA crosslink sites.  This method, termed CIMS and CITS analysis, allows us to '''map protein-RNA interactions at single nucleotide resolution'''.  We are using this powerful approach to obtain unprecedented details about how the specificity of protein-RNA interaction is determined.
+
            </div>
  
*Moore, M.*, Zhang, C.*, Gantman, E.C., Mele, A., Darnell, J.C., Darnell, R.B. 2014. Mapping Argonaute and conventional RNA-binding protein interactions with RNA at single-nucleotide resolution using HITS-CLIP and CIMS analysis. Nat Protocols.  9:263-293. ([[CIMS_Documentation|Software]])
+
            <div>
 +
                <a u=image href="https://www.cell.com/cell-reports/abstract/S2211-1247(14)00084-9" rel="nofollow"><img u="image" src="/data/images/slideshow/Rbfox.png" width="400" height="200" /></a>
 +
            </div>
  
*Zhang, C.†, Darnell, R.B.† 2011. Mapping in vivo protein-RNA interactions at single-nucleotide resolution from HITS-CLIP data. ''Nat Biotech'', 29:607-614.
+
            <div>
 +
                <a u=image href="http://zhanglab.c2b2.columbia.edu/index.php/CIMS" rel="nofollow"><img u="image" src="/data/images/slideshow/CIMS.png" width="400" height="200" /></a>
 +
            </div>
  
 +
            <div>
 +
                <a u=image href="https://sfari.org" rel="nofollow"><img u="image" src="/data/images/slideshow/SFARI.png" width="400" height="200" /></a>
 +
            </div>
  
|
+
            <div>
[[File:crosslink.png|right|300px]]
+
                <a u=image href="http://zhanglab.c2b2.columbia.edu/index.php/MCarts_Documentation" rel="nofollow"><img u="image" src="/data/images/slideshow/mCarts.png" width="400" height="200" /></a>
 +
            </div>
 +
<!--
 +
            <div>
 +
                <a u=image href="http://zhanglab.c2b2.columbia.edu/index.php/OLego" rel="nofollow"><img u="image" src="/data/images/slideshow/olego.png" width="400" height="200" /></a>
 +
            </div>
  
|}
 
  
==Organizational principles and functional impact of neuronal RNA-regulatory networks==
+
            <div>
 +
                <a u=image href="http://zhanglab.c2b2.columbia.edu/index.php/Openings" rel="nofollow"><img u="image" src="/data/images/slideshow/hiring.png" width="400" height="200" /></a>
 +
            </div>
 +
//-->
 +
        </div>
 +
        <a style="display:none" href="http://slideshow.jssor.com">Javascript Slideshow</a>
 +
        <!-- Trigger -->
 +
        <script>
 +
            jssor_slider1_starter('slider1_container');
 +
        </script>
 +
    </div>
  
{|class="zebra wikitable" width="100%" style="border:0px solid; border-collapse:collapse;"
+
</center>
 +
</html>
  
|-
 
|
 
To understand the function of RNA regulatory network, a first step is to infer the structure of such networks, which is challenging due in part to the degeneracy and dynamic nature of the splicing code.  We pioneered the development of '''integrative analysis of splicing regulatory networks''', which has enabled us to identify alternative exons regulated by specific RBPs with unprecedented accuracy and sensitivity.  In brief, our strategy was to identify altered splicing upon genetic RBP depletion, although such changes can be either direct or indirect.  The latter was distinguished by mapping the precise RBP binding sites in vivo using HITS-CLIP.  These data were then formally combined using a Bayesian network to determine high-confidence, direct target transcripts25,28.  Studies using this paradigm demonstrated the concerted regulation of hundreds of alternative exons by individual neuronal RBPs.  Investigation of the resulting networks allow us to make unexpected findings such as coupling of splicing with post-translational modifications.
 
  
*Weyn-Vanhentenryck,S.,M.*, Mele,A.*, Yan,Q.*, Sun,S., Farny,N., Zhang,Z., Xue,C., Herre,M., Silver,P.A., Zhang,M.Q., Krainer,A.R., Darnell,R.B.†, Zhang,C. † 2014.  HITS-CLIP and integrative modeling define the Rbfox splicing-regulatory network linked to brain development and autism. ''Cell Rep'', 6:1139-1152.
+
'''Introduction of the Zhang Laboratory'''
*Zhang, C.†, Frias, M.A., Mele, A., Ruggiu, M., Eom, T., Marney, C.B., Wang, H., Licatalosi, D.D., Fak, J.J., Darnell, R.B.† 2010. Integrative modeling defines the Nova splicing-regulatory network and its combinatorial controls. ''Science'', 329: 439-443.
+
*Zhang, C.*, Zhang, Z.*, Castle, J., Sun, S., Johnson, J., Krainer, A.R. and Zhang, M.Q. 2008. Defining the regulatory network of the tissue-specific splicing factors Fox-1 and Fox-2. ''Genes Dev'', 22:2550-2563.
+
  
|
+
We are part of the [http://systemsbiology.columbia.edu Department of Systems Biology], the [http://cpmcnet.columbia.edu/dept/gsas/biochem/ Department of Biochemistry and Molecular Biophysics], and the [http://www.columbiamnc.org/ Motor Neuron Center] at [http://http://www.cumc.columbia.edu Columbia University Medical Center].
[[File:bnet.png|right|300px]]
+
  
|}
+
We are fascinated by the complexity of the mammalian nervous system and its underlying molecular mechanisms.  While mammals have a similar number of genes compared to phenotypically simpler organisms (such as worms), one apparent feature of mammalian genes is their more complicated gene structures, providing an opportunity for sophisticated regulation at the RNA level. 
  
==RNA regulatory networks in neural development==
+
The focus of the Zhang lab is to dissect RNA regulatory networks in the nervous system as a way to understand the mammalian complexity manifested in evolutionary-developmental (evo-devo) processes and in several neuronal disorders. We work on a range of problems towards the goal, including mechanistic understanding of the specificity of protein-RNA interactions, organizational principles of RNA regulatory networks, and functional implication of RNA regulation in neural development and in certain pathologic contexts (such as autism and neurodegenerative disorders).  The Zhang lab has a mixed dry and wet setup. We take advantage of different model systems, including mouse models and in vitro neural differentiation of embryonic stem cells, and a combination of high-throughput data-driven and hypothesis-driven approaches.
  
{|class="zebra wikitable" width="100%" style="border:0px solid; border-collapse:collapse;"
 
  
|-
+
'''Lab News'''
|style="vertical-align: top;"|
+
For our current work, one focus is to investigate systematically how multiple RBPs work together to drive '''dynamic regulation during neurodevelopment'''. We aim to find predictive rules of combinatorial regulation, and how groups of RBPs define subsets of target transcripts that are functional distinct.  To this end, we rely on the structure of RBPs defined by integrative modeling approaches, and statistical inference to determine the correlation structure underlying time series transcriptome data.
+
  
Another exciting direction is the use of embryonic stem cells (ESCs) and in vitro differentiation of neurons from (ESCs). We collaborate with Hynek Wichterle group at Columbia, who developed and optimized the directed, in vitro differentiation of motor neurons, a group of nerve cells through which the brain controls muscle contraction. Motor neurons are also the primary targets in several devastating neuron degenerative diseases including amyotrophic lateral sclerosis (ALS) and spinal muscular satrapy (SMA). This system has two key advantages: 1) the differential process recapitulate many key aspects of in vivo motor neuron development; 2) the use of ES cells makes it possible to leverage genome engineering techniques to perturb RNA regulatory networks. By dissecting RNA regulatory networks in detail, we hope to obtain a deeper understanding of their functional impact and the underlying regulatory mechanisms in this well defined, clinically relevant cell type.
+
* 03/01/2016. Congratulate Ankeeta Shah on winning the 2016 SURF/Amgen fellowship!
 +
* 06/19/2105. Chaolin Zhang received an R01 award from NIH/NINDS
 +
* 03/06/2015. Discovery of new AS exons in the brain published on PNAS
 +
* 07/29/2014. Chaolin Zhang received a 3 year Research Award from Simons Foundation
 +
* 03/06/2014. Rbfox CLIP and integrative modeling paper published on Cell Reports
 +
* 01/10/2014. Step by step guide of CIMS analysis published on Nature Protocols
 +
* 09/24/2013. Chaolin Zhang received an Explorer Award from Simons Foundation
 +
* 04/26/2013. mCarts paper published on NAR
 +
* 04/26/2013. OLego paper published on NAR
  
|
 
[[File:eb.png|right|300px]]
 
  
|}
 
  
==Variation of RNA-regulatory networks in evolution, human populations and in neuronal disorders==
+
<html>
{|class="zebra wikitable" width="100%" style="border:0px solid; border-collapse:collapse;"
+
<div align="center">
  
|-
+
<a href="http://sbi.c2b2.columbia.edu/"><img src="/data/images/CSB.png" width="147" height="40" /></a>
|style="vertical-align: top;"|
+
<a href="http://www.columbiamnc.org/"><img src="/data/images/mnc_logo.gif" width="122" height="35" /></a>
Another related direction of our lab is to evaluate the impact of '''mutations on RNA regulation''' in normal physiology or disease. Our study spans three contexts: comparison of different species (e.g. rodents and primates), different human populations, and patients affected by neurological diseases and normal controls. Such study is facilitated by our ability to determine protein-RNA interactions at a high resolution and distinction of functional vs. nonfunctional interactions. We will apply this strategy to parallel systems in different species that are directly comparable, large transcriptome profiles of human populations generated by consortium efforts, and mutations identified by genomic sequencing compiled from the public domain and collaborators.
+
<a href="http://www.c2b2.columbia.edu"><img src="/data/images/C2B2_logo.png" width="215" height="60" /></a> <p>
  
 
+
</div>
|
+
</html>
[[File:evo.png|right|300px]]
+
 
+
|}
+

Revision as of 14:20, 10 March 2016


Javascript Slideshow


Introduction of the Zhang Laboratory

We are part of the Department of Systems Biology, the Department of Biochemistry and Molecular Biophysics, and the Motor Neuron Center at Columbia University Medical Center.

We are fascinated by the complexity of the mammalian nervous system and its underlying molecular mechanisms. While mammals have a similar number of genes compared to phenotypically simpler organisms (such as worms), one apparent feature of mammalian genes is their more complicated gene structures, providing an opportunity for sophisticated regulation at the RNA level.

The focus of the Zhang lab is to dissect RNA regulatory networks in the nervous system as a way to understand the mammalian complexity manifested in evolutionary-developmental (evo-devo) processes and in several neuronal disorders. We work on a range of problems towards the goal, including mechanistic understanding of the specificity of protein-RNA interactions, organizational principles of RNA regulatory networks, and functional implication of RNA regulation in neural development and in certain pathologic contexts (such as autism and neurodegenerative disorders). The Zhang lab has a mixed dry and wet setup. We take advantage of different model systems, including mouse models and in vitro neural differentiation of embryonic stem cells, and a combination of high-throughput data-driven and hypothesis-driven approaches.


Lab News

  • 03/01/2016. Congratulate Ankeeta Shah on winning the 2016 SURF/Amgen fellowship!
  • 06/19/2105. Chaolin Zhang received an R01 award from NIH/NINDS
  • 03/06/2015. Discovery of new AS exons in the brain published on PNAS
  • 07/29/2014. Chaolin Zhang received a 3 year Research Award from Simons Foundation
  • 03/06/2014. Rbfox CLIP and integrative modeling paper published on Cell Reports
  • 01/10/2014. Step by step guide of CIMS analysis published on Nature Protocols
  • 09/24/2013. Chaolin Zhang received an Explorer Award from Simons Foundation
  • 04/26/2013. mCarts paper published on NAR
  • 04/26/2013. OLego paper published on NAR