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Investigating the Function of Canonical Polycomb Repressive Complex 1 Phase Separation in Epigenetic Regulation
Investigating the Function of Canonical Polycomb Repressive Complex 1 Phase Separation in ...
Investigating the Function of Canonical Polycomb Repressive Complex 1 Phase Separation in Epigenetic Regulation

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211151443
ISBN  
9798382784991
DDC  
574
저자명  
Oei, Theresa Ann.
서명/저자  
Investigating the Function of Canonical Polycomb Repressive Complex 1 Phase Separation in Epigenetic Regulation
발행사항  
[Sl] : Harvard University, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
155 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
주기사항  
Advisor: Kingston, Robert E.
학위논문주기  
Thesis (Ph.D.)--Harvard University, 2024.
초록/해제  
요약Polycomb group (PcG) proteins are key developmental regulators involved in gene repression and the maintenance of cell identity. They are a dynamic part of facultative chromatin found clustered in the nucleus as Polycomb bodies. Canonical Polycomb Repressive Complex 1 (cPRC1) is hypothesized to facilitate the silencing of chromatin by compaction and phase separation. The CBX subunit recruits cPRC1 to chromatin and has been shown to contribute to PRC1 condensate formation. The goal of my thesis work was to characterize the phase separation of PRC1 driven by paralogs of the CBX family of proteins and to demonstrate the function of phase separation in PRC1 epigenetic regulation.In Chapter 1, I will introduce PRC1 and its role in gene repression and development. I will also introduce the concept of liquid liquid phase separation and its proposed role in transcriptional control. Additionally, I will describe the many ways in which PcG proteins, such as the CBXs, are misregulated in cancer.In Chapter 2, I will describe my characterization of the CBX4 and CBX8 proteins and their phase separation activity both in vitro and in cells. I will show how positively charged amino acids in the intrinsically disordered regions of these proteins contribute to their condensate behavior and compare the dynamics of CBX4 and CBX8 to CBX2 in cells.In Chapter 3, I will share an adaptation of my submitted manuscript demonstrating that heterologous phase separation can rescue PRC1 function of a CBX2 phase separation mutant in a cancer model system.In Chapter 4, I will summarize the conclusions from my thesis research and discuss the ways in which this work advances the field of epigenetic regulation. I will also explore potential future directions for further understanding the mechanisms of CBX phase separation in Polycomb-mediated gene repression.
일반주제명  
Molecular biology
일반주제명  
Cellular biology
일반주제명  
Oncology
키워드  
Condensates
키워드  
Epigenetics
키워드  
Phase separation
키워드  
Polycomb group
키워드  
Cancer
기타저자  
Harvard University Chemical Biology
기본자료저록  
Dissertations Abstracts International. 85-12B.
전자적 위치 및 접속  
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MARC

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■006m          o    d                
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■020    ▼a9798382784991
■035    ▼a(MiAaPQ)AAI31296271
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a574
■1001  ▼aOei,  Theresa  Ann.▼0(orcid)0000-0002-2065-4760
■24510▼aInvestigating  the  Function  of  Canonical  Polycomb  Repressive  Complex  1  Phase  Separation  in  Epigenetic  Regulation
■260    ▼a[Sl]▼bHarvard  University▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a155  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-12,  Section:  B.
■500    ▼aAdvisor:  Kingston,  Robert  E.
■5021  ▼aThesis  (Ph.D.)--Harvard  University,  2024.
■520    ▼aPolycomb  group  (PcG)  proteins  are  key  developmental  regulators  involved  in  gene  repression  and  the  maintenance  of  cell  identity.  They  are  a  dynamic  part  of  facultative  chromatin  found  clustered  in  the  nucleus  as  Polycomb  bodies.  Canonical  Polycomb  Repressive  Complex  1  (cPRC1)  is  hypothesized  to  facilitate  the  silencing  of  chromatin  by  compaction  and  phase  separation.  The  CBX  subunit  recruits  cPRC1  to  chromatin  and  has  been  shown  to  contribute  to  PRC1  condensate  formation.  The  goal  of  my  thesis  work  was  to  characterize  the  phase  separation  of  PRC1  driven  by  paralogs  of  the  CBX  family  of  proteins  and  to  demonstrate  the  function  of  phase  separation  in  PRC1  epigenetic  regulation.In  Chapter  1,  I  will  introduce  PRC1  and  its  role  in  gene  repression  and  development.  I  will  also  introduce  the  concept  of  liquid  liquid  phase  separation  and  its  proposed  role  in  transcriptional  control.  Additionally,  I  will  describe  the  many  ways  in  which  PcG  proteins,  such  as  the  CBXs,  are  misregulated  in  cancer.In  Chapter  2,  I  will  describe  my  characterization  of  the  CBX4  and  CBX8  proteins  and  their  phase  separation  activity  both  in  vitro  and  in  cells.  I  will  show  how  positively  charged  amino  acids  in  the  intrinsically  disordered  regions  of  these  proteins  contribute  to  their  condensate  behavior  and  compare  the  dynamics  of  CBX4  and  CBX8  to  CBX2  in  cells.In  Chapter  3,  I  will  share  an  adaptation  of  my  submitted  manuscript  demonstrating  that  heterologous  phase  separation  can  rescue  PRC1  function  of  a  CBX2  phase  separation  mutant  in  a  cancer  model  system.In  Chapter  4,  I  will  summarize  the  conclusions  from  my  thesis  research  and  discuss  the  ways  in  which  this  work  advances  the  field  of  epigenetic  regulation.  I  will  also  explore  potential  future  directions  for  further  understanding  the  mechanisms  of  CBX  phase  separation  in  Polycomb-mediated  gene  repression.
■590    ▼aSchool  code:  0084.
■650  4▼aMolecular  biology
■650  4▼aCellular  biology
■650  4▼aOncology
■653    ▼aCondensates
■653    ▼aEpigenetics
■653    ▼aPhase  separation
■653    ▼aPolycomb  group
■653    ▼aCancer
■690    ▼a0307
■690    ▼a0379
■690    ▼a0992
■71020▼aHarvard  University▼bChemical  Biology.
■7730  ▼tDissertations  Abstracts  International▼g85-12B.
■790    ▼a0084
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17161774▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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