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Development of CRISPR-Based Tools for the Dissection of Chromatin Organization and Dynamics
Development of CRISPR-Based Tools for the Dissection of Chromatin Organization and Dynamic...
Development of CRISPR-Based Tools for the Dissection of Chromatin Organization and Dynamics

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자료유형  
 학위논문 서양
최종처리일시  
20250211151939
ISBN  
9798384463269
DDC  
574.191
저자명  
Chang, Yi-Che.
서명/저자  
Development of CRISPR-Based Tools for the Dissection of Chromatin Organization and Dynamics
발행사항  
[Sl] : Princeton University, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
141 p
주기사항  
Source: Dissertations Abstracts International, Volume: 86-04, Section: B.
주기사항  
Advisor: Brangwynne, Clifford P.
학위논문주기  
Thesis (Ph.D.)--Princeton University, 2024.
초록/해제  
요약Eukaryotic cells compartmentalize intracellular components to segregate essential biological functions. While membrane-bound organelles have traditionally served this purpose, liquid-liquid phase separation (LLPS) emerges as a complementary mechanism in cellular spatial organization without membrane-bound structures. This dissertation investigates LLPS' roles in nucleus and genome organization by segregating functionally distinct nuclear compartments, each featuring a distinct set of biochemical reactions. We first discuss the development of CasDrop, a CRISPR/Cas9-based optogenetic tool, and how it can be used to study condensate-genome interactions. Specific focus is given to how transcriptionally active and inactive condensates can exclude each other, along with chromatin compartments enriched in active or inactive proteins. These chemical and mechanical effects can impact the local dynamics of the genome structure and its functional states. We further demonstrate that condensate surface tension can be harnessed to rapidly restructure genome organization. Finally, we reveal the complex, heterogenous organization within euchromatin; and probed its chromatin dynamics to investigate the correlation between transcriptional activity and chromatin dynamics at a genome-wide scale.
일반주제명  
Biophysics
일반주제명  
Bioengineering
일반주제명  
Cellular biology
키워드  
Eukaryotic cells
키워드  
Genome structure
키워드  
Heterogenous organization
키워드  
Chromatin dynamics
키워드  
Optogenetic tool
기타저자  
Princeton University Chemistry
기본자료저록  
Dissertations Abstracts International. 86-04B.
전자적 위치 및 접속  
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■020    ▼a9798384463269
■035    ▼a(MiAaPQ)AAI31302040
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a574.191
■1001  ▼aChang,  Yi-Che.
■24510▼aDevelopment  of  CRISPR-Based  Tools  for  the  Dissection  of  Chromatin  Organization  and  Dynamics
■260    ▼a[Sl]▼bPrinceton  University▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a141  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  86-04,  Section:  B.
■500    ▼aAdvisor:  Brangwynne,  Clifford  P.
■5021  ▼aThesis  (Ph.D.)--Princeton  University,  2024.
■520    ▼aEukaryotic  cells  compartmentalize  intracellular  components  to  segregate  essential  biological  functions.  While  membrane-bound  organelles  have  traditionally  served  this  purpose,  liquid-liquid  phase  separation  (LLPS)  emerges  as  a  complementary  mechanism  in  cellular  spatial  organization  without  membrane-bound  structures.  This  dissertation  investigates  LLPS'  roles  in  nucleus  and  genome  organization  by  segregating  functionally  distinct  nuclear  compartments,  each  featuring  a  distinct  set  of  biochemical  reactions.  We  first  discuss  the  development  of  CasDrop,  a  CRISPR/Cas9-based  optogenetic  tool,  and  how  it  can  be  used  to  study  condensate-genome  interactions.  Specific  focus  is  given  to  how  transcriptionally  active  and  inactive  condensates  can  exclude  each  other,  along  with  chromatin  compartments  enriched  in  active  or  inactive  proteins.  These  chemical  and  mechanical  effects  can  impact  the  local  dynamics  of  the  genome  structure  and  its  functional  states.  We  further  demonstrate  that  condensate  surface  tension  can  be  harnessed  to  rapidly  restructure  genome  organization.  Finally,  we  reveal  the  complex,  heterogenous  organization  within  euchromatin;  and  probed  its  chromatin  dynamics  to  investigate  the  correlation  between  transcriptional  activity  and  chromatin  dynamics  at  a  genome-wide  scale.
■590    ▼aSchool  code:  0181.
■650  4▼aBiophysics
■650  4▼aBioengineering
■650  4▼aCellular  biology
■653    ▼aEukaryotic  cells
■653    ▼aGenome  structure
■653    ▼aHeterogenous  organization
■653    ▼aChromatin  dynamics
■653    ▼aOptogenetic  tool
■690    ▼a0786
■690    ▼a0202
■690    ▼a0379
■71020▼aPrinceton  University▼bChemistry.
■7730  ▼tDissertations  Abstracts  International▼g86-04B.
■790    ▼a0181
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17162160▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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