본문

서브메뉴

High-Information Phenotypic Characterization of the Effect of Ionizing Radiation on Human Cells Using Rich Phenotypes From Perturb-Seq
High-Information Phenotypic Characterization of the Effect of Ionizing Radiation on Human ...
High-Information Phenotypic Characterization of the Effect of Ionizing Radiation on Human Cells Using Rich Phenotypes From Perturb-Seq

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211153035
ISBN  
9798346876786
DDC  
574
저자명  
Wong, Garrett.
서명/저자  
High-Information Phenotypic Characterization of the Effect of Ionizing Radiation on Human Cells Using Rich Phenotypes From Perturb-Seq
발행사항  
[Sl] : University of California, San Francisco, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
52 p
주기사항  
Source: Dissertations Abstracts International, Volume: 86-06, Section: B.
주기사항  
Includes supplementary digital materials.
주기사항  
Advisor: Ntranos, Vasilis.
학위논문주기  
Thesis (Ph.D.)--University of California, San Francisco, 2024.
초록/해제  
요약Ionizing radiation is employed broadly in oncology, but has a narrow therapeutic window arising from nonspecifically induced genomic damage in both healthy and cancerous cells. We employ genome-scale CRISPRi perturb-seq across millions of human cells alongside proliferation screens to profile all expressed genes' effect on heterogenous cellular responses to ionizing radiation in the human chronic myelogenous leukemia cell line K562. We identify undercharacterized radiation sensitizing genes and leverage rich transcriptomic phenotypes to assign putative functional roles based on clustering. We find perturbations which induce radiation-specific responses in single-cell transcriptomic phenotypes like cell cycle state and chromosomal instability, and show how the stressor environment reveals the role of regulatory programs invisible without radiation. A followup validation perturb-seq experiment was used to determine the replicability and broader applicability of these findings, bolstering our confidence in our generation of high-quality transcriptomic profiles to CRISPRi perturbation and ionizing radiation.
일반주제명  
Biology
일반주제명  
Bioinformatics
일반주제명  
Genetics
일반주제명  
Cellular biology
일반주제명  
Molecular biology
키워드  
Ionizing radiation
키워드  
Perturb-seq
키워드  
Human cells
키워드  
Phenotypes
키워드  
Perturbations
기타저자  
University of California, San Francisco Biological and Medical Informatics
기본자료저록  
Dissertations Abstracts International. 86-06B.
전자적 위치 및 접속  
로그인 후 원문을 볼 수 있습니다.

MARC

 008250123s2024        us                              c    eng  d
■001000017164715
■00520250211153035
■006m          o    d                
■007cr#unu||||||||
■020    ▼a9798346876786
■035    ▼a(MiAaPQ)AAI31637498
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a574
■1001  ▼aWong,  Garrett.▼0(orcid)0000-0002-1840-2628
■24510▼aHigh-Information  Phenotypic  Characterization  of  the  Effect  of  Ionizing  Radiation  on  Human  Cells  Using  Rich  Phenotypes  From  Perturb-Seq
■260    ▼a[Sl]▼bUniversity  of  California,  San  Francisco▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a52  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  86-06,  Section:  B.
■500    ▼aIncludes  supplementary  digital  materials.
■500    ▼aAdvisor:  Ntranos,  Vasilis.
■5021  ▼aThesis  (Ph.D.)--University  of  California,  San  Francisco,  2024.
■520    ▼aIonizing  radiation  is  employed  broadly  in  oncology,  but  has  a  narrow  therapeutic  window  arising  from  nonspecifically  induced  genomic  damage  in  both  healthy  and  cancerous  cells.  We  employ  genome-scale  CRISPRi  perturb-seq  across  millions  of  human  cells  alongside  proliferation  screens  to  profile  all  expressed  genes'  effect  on  heterogenous  cellular  responses  to  ionizing  radiation  in  the  human  chronic  myelogenous  leukemia  cell  line  K562.  We  identify  undercharacterized  radiation  sensitizing  genes  and  leverage  rich  transcriptomic  phenotypes  to  assign  putative  functional  roles  based  on  clustering.  We  find  perturbations  which  induce  radiation-specific  responses  in  single-cell  transcriptomic  phenotypes  like  cell  cycle  state  and  chromosomal  instability,  and  show  how  the  stressor  environment  reveals  the  role  of  regulatory  programs  invisible  without  radiation.  A  followup  validation  perturb-seq  experiment  was  used  to  determine  the  replicability  and  broader  applicability  of  these  findings,  bolstering  our  confidence  in  our  generation  of  high-quality  transcriptomic  profiles  to  CRISPRi  perturbation  and  ionizing  radiation.
■590    ▼aSchool  code:  0034.
■650  4▼aBiology
■650  4▼aBioinformatics
■650  4▼aGenetics
■650  4▼aCellular  biology
■650  4▼aMolecular  biology
■653    ▼aIonizing  radiation
■653    ▼aPerturb-seq
■653    ▼aHuman  cells
■653    ▼aPhenotypes
■653    ▼aPerturbations
■690    ▼a0306
■690    ▼a0715
■690    ▼a0369
■690    ▼a0379
■690    ▼a0307
■71020▼aUniversity  of  California,  San  Francisco▼bBiological  and  Medical  Informatics.
■7730  ▼tDissertations  Abstracts  International▼g86-06B.
■790    ▼a0034
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17164715▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

미리보기

내보내기

chatGPT토론

Ai 추천 관련 도서


    신착도서 더보기
    최근 3년간 통계입니다.

    소장정보

    • 예약
    • 소재불명신고
    • 나의폴더
    • 우선정리요청
    • 비도서대출신청
    • 야간 도서대출신청
    소장자료
    등록번호 청구기호 소장처 대출가능여부 대출정보
    TF11913 전자도서 대출가능 마이폴더 부재도서신고 비도서대출신청 야간 도서대출신청

    * 대출중인 자료에 한하여 예약이 가능합니다. 예약을 원하시면 예약버튼을 클릭하십시오.

    해당 도서를 다른 이용자가 함께 대출한 도서

    관련 인기도서

    로그인 후 이용 가능합니다.