User Tools

Site Tools


4dn:phase1:2017_annual_meeting:integrated_approaches_workshop

Differences

This shows you the differences between two versions of the page.

Link to this comparison view

Both sides previous revision Previous revision
Next revision
Previous revision
4dn:phase1:2017_annual_meeting:integrated_approaches_workshop [2019/01/23 09:55]
oh
4dn:phase1:2017_annual_meeting:integrated_approaches_workshop [2025/04/22 16:21] (current)
Line 1: Line 1:
-Integrated approaches workshop 
  
-|_PARA__TABLE_INS_WORKSHOP_PARA__TABLE_INS__PARA__TABLE_INS_Integrated ​Approaches for Spatial and Temporal Mapping of Gene Activity in Cells and Tissues_PARA__TABLE_INS__PARA__TABLE_INS_SEPTEMBER ​20, 2017_PARA__TABLE_INS__PARA__TABLE_INS_LOCATION: Bethesda North Marriott Hotel ( CKGE_TMP_i ​Salon F-G CKGE_TMP_i ​)_PARA__TABLE_INS__PARA__TABLE_INS_[[https://​docs.google.com/​document/​d/​1yOrIYJYOVdIHwdttpT5mx2523z9AiyXgdHWiXG06LJM/​edit?​usp=sharing|PROGRAM AGENDA]]_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​1:00 Introductory statements; Rob Singer_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​The purpose of this workshop is to introduce expertise and technology to the consortium that would be important to help achieve the 4DN goals. The workshop will focus on spatial and temporal aspects of chromatin structure that lead to activation. The goal would be to: a) identify areas of collaboration for the 4DN network, 2) identify potential areas of collaboration with other programs, 3) provide an opportunity to have a dialog between 4DN investigators and other researchers working in this field._PARA__TABLE_INS_ _PARA__TABLE_INS_ ​1:05 Gary Karpen (Berkeley). "Phase transitions drive chromatin domain formation"​_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​Gary has been assessing the role of chromatin in gene activation. His recent work demonstrates that chromatin domains undergo phase transitions. ( CKGE_TMP_i ​Nature ​CKGE_TMP_i ​2017, PMID:​28636597)_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​1:30 Xiaowei Zhuang (Harvard). “Imaging the spatial organization of the chromosome and the transcriptome in single cells”._PARA__TABLE_INS_ _PARA__TABLE_INS_ ​Xiaowei has been developing superresolution methods for high resolution imaging of chromatin and their compartments over time ( CKGE_TMP_i ​Science ​CKGE_TMP_i ​2016, PMCID PMC4991974)_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​2:00 Michael Levine (Princeton) “Promoter-enhancer interactions as a model for gene activation”_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​Michael has been investigating the spatial and temporal events concerning promoters and enhancers in living embryos. They stand as a model for how 4D DNA folding can activate transcriptional bursting ( CKGE_TMP_i ​Cell CKGE_TMP_i ​2016, PMCID:​PMC4970759)_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​2:30 break_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​3:00 Rifka Vlijm (Heidelberg) “Imaging nuclear structural changes using STED microscopy”._PARA__TABLE_INS_ _PARA__TABLE_INS_ ​Rifka has been working with Stefan Hell to develop dyes for superresolution STED microscopy for investigating nuclear events in living cells and embryos. ( CKGE_TMP_i ​Chemistry ​CKGE_TMP_i ​, 2017, PMID 28370443)_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​3:30 Luke Lavis (Janelia Research Campus) "New dyes for imaging nuclear structures in real time"._PARA__TABLE_INS_ _PARA__TABLE_INS_ ​Luke is part of the senior leadership at Janelia. He is a leading organic chemist and responsible for generating the fluorogenic JF dyes that are now widely used for biological imaging. He is currently developing new variants that are brighter with lower phototoxicity. These dyes will eventually make it possible to image cells for longer times with less photodamage ( CKGE_TMP_i ​Nature Methods ​CKGE_TMP_i ​2016, PMID:​27776112)_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​4:00 Discussion: Joan Ritland, Job Dekker, Andy Belmont, David Gilbert, Jan Liphardt, Rob Singer and Richard ​Conroy_PARA__TABLE_INS_ _PARA__TABLE_INS_ ​The purpose of this session would be to discuss and come up with suggested Consortium activities for: 1) the temporal dynamics of nuclear architecture,​ 2) nuclear structure in primary cells in a 3D tissue environment._PARA__TABLE_INS_ _PARA__TABLE_INS_ ​5:00 Adjourn_PARA__TABLE_INS_ | + 
-| |+**WORKSHOP** 
 + 
 +**Integrated ​Approaches for Spatial and Temporal Mapping of Gene Activity in Cells and Tissues** 
 + 
 +SEPTEMBER ​20, 2017 
 + 
 +LOCATION: Bethesda North Marriott Hotel (Salon F-G) 
 + 
 +[[https://​docs.google.com/​document/​d/​1yOrIYJYOVdIHwdttpT5mx2523z9AiyXgdHWiXG06LJM/​edit?​usp=sharing|PROGRAM AGENDA]] 
 + 
 +1:00   ​Introductory statements; Rob Singer 
 + 
 +  * The purpose of this workshop is to introduce expertise and technology to the consortium that would be important to help achieve the 4DN goals. The workshop will focus on spatial and temporal aspects of chromatin structure that lead to activation. The goal would be to: a) identify areas of collaboration for the 4DN network, 2) identify potential areas of collaboration with other programs, 3) provide an opportunity to have a dialog between 4DN investigators and other researchers working in this field. 
 + 
 +1:05   ​Gary Karpen (Berkeley). ​**"Phase transitions drive chromatin domain formation"​** 
 + 
 +  * Gary has been assessing the role of chromatin in gene activation. His recent work demonstrates that  chromatin domains undergo phase transitions. (//Nature// 2017, PMID:​28636597) 
 + 
 +1:30  Xiaowei Zhuang (Harvard). ​ **“Imaging the spatial organization of the chromosome and the transcriptome in single cells”.** 
 + 
 +  * Xiaowei has been developing superresolution methods for high resolution imaging of chromatin and their compartments over time (//Science ​//2016, PMCID PMC4991974) 
 + 
 +2:00   ​Michael Levine (Princeton) ​**“Promoter-enhancer interactions as a model for gene activation”** 
 + 
 +  * Michael has been investigating the spatial and temporal events concerning promoters and enhancers in living embryos. They stand as a model for how 4D DNA folding can activate transcriptional bursting (//Cell// 2016, PMCID:​PMC4970759) 
 + 
 +2:30 break 
 + 
 +3:00   ​Rifka Vlijm (Heidelberg) ​** “Imaging nuclear structural changes using STED microscopy”.** 
 + 
 +  * Rifka has been working with Stefan Hell to develop dyes for superresolution STED microscopy for investigating nuclear events in living cells and embryos. (//Chemistry//, 2017, PMID 28370443) 
 + 
 +3:30 Luke Lavis (Janelia Research Campus)** "New dyes for imaging nuclear structures in real time".** 
 + 
 +  * Luke is part of the senior leadership at Janelia. He is a leading organic chemist and responsible for generating the fluorogenic JF dyes that are now widely used for biological imaging. He is currently developing new variants that are brighter with lower phototoxicity. These dyes will eventually make it possible to image cells for longer times with less photodamage (//Nature Methods// 2016, PMID:​27776112) 
 + 
 +4:00  Discussion: Joan Ritland, Job Dekker, Andy Belmont, David Gilbert, Jan Liphardt, Rob Singer and Richard ​Conroy 
 + 
 +  * ** The purpose of this session would be to discuss and come up with suggested Consortium activities for: 1) the temporal dynamics of nuclear architecture,​ 2) nuclear structure in primary cells in a 3D tissue environment. ​** 
 +5:00        ​Adjourn
  
  
4dn/phase1/2017_annual_meeting/integrated_approaches_workshop.1548266119.txt.gz · Last modified: 2025/04/22 16:21 (external edit)