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Measuring Messenger RNA Stability Across Developmental Stages and Cell Types Throughout Embryogenesis
Measuring Messenger RNA Stability Across Developmental Stages and Cell Types Throughout Em...
Measuring Messenger RNA Stability Across Developmental Stages and Cell Types Throughout Embryogenesis

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자료유형  
 학위논문 서양
최종처리일시  
20250211152046
ISBN  
9798384025092
DDC  
575
저자명  
Peng, Felicia.
서명/저자  
Measuring Messenger RNA Stability Across Developmental Stages and Cell Types Throughout Embryogenesis
발행사항  
[Sl] : University of Pennsylvania, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
122 p
주기사항  
Source: Dissertations Abstracts International, Volume: 86-02, Section: B.
주기사항  
Advisor: Murray, John I.
학위논문주기  
Thesis (Ph.D.)--University of Pennsylvania, 2024.
초록/해제  
요약During embryonic development, cells undergo dynamic changes in gene expression that are required for appropriate cell fate specification. Although both transcription and mRNA degradation contribute to gene expression dynamics, patterns of mRNA decay are less well-understood. Here we directly measured spatiotemporally resolved mRNA decay rates transcriptome-wide throughout C. elegans embryogenesis by transcription inhibition followed by bulk and single-cell RNA-sequencing. This allowed us to calculate mRNA half-lives within specific cell types and developmental stages and identify differentially regulated mRNA decay throughout embryonic development. We identified transcript features that are correlated with mRNA stability and found that mRNA decay rates are associated with distinct peaks in gene expression over time. Moreover, we provide evidence that, on average, mRNA is more stable in the germline compared to in the soma and in later embryonic stages compared to in earlier stages. This work suggests that differential mRNA decay across cell states and time helps to shape developmental gene expression, and it provides a valuable resource for studies of mRNA turnover regulatory mechanisms.
일반주제명  
Genetics
일반주제명  
Cellular biology
일반주제명  
Molecular biology
일반주제명  
Developmental biology
키워드  
mRNA decay
키워드  
Developmental stages
키워드  
Embryogenesis
키워드  
Embryonic development
키워드  
Cell types
기타저자  
University of Pennsylvania Cell and Molecular Biology
기본자료저록  
Dissertations Abstracts International. 86-02B.
전자적 위치 및 접속  
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MARC

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■020    ▼a9798384025092
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■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a575
■1001  ▼aPeng,  Felicia.
■24510▼aMeasuring  Messenger  RNA  Stability  Across  Developmental  Stages  and  Cell  Types  Throughout  Embryogenesis
■260    ▼a[Sl]▼bUniversity  of  Pennsylvania▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a122  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  86-02,  Section:  B.
■500    ▼aAdvisor:  Murray,  John  I.
■5021  ▼aThesis  (Ph.D.)--University  of  Pennsylvania,  2024.
■520    ▼aDuring  embryonic  development,  cells  undergo  dynamic  changes  in  gene  expression  that  are  required  for  appropriate  cell  fate  specification.  Although  both  transcription  and  mRNA  degradation  contribute  to  gene  expression  dynamics,  patterns  of  mRNA  decay  are  less  well-understood.  Here  we  directly  measured  spatiotemporally  resolved  mRNA  decay  rates  transcriptome-wide  throughout  C.  elegans  embryogenesis  by  transcription  inhibition  followed  by  bulk  and  single-cell  RNA-sequencing.  This  allowed  us  to  calculate  mRNA  half-lives  within  specific  cell  types  and  developmental  stages  and  identify  differentially  regulated  mRNA  decay  throughout  embryonic  development.  We  identified  transcript  features  that  are  correlated  with  mRNA  stability  and  found  that  mRNA  decay  rates  are  associated  with  distinct  peaks  in  gene  expression  over  time.  Moreover,  we  provide  evidence  that,  on  average,  mRNA  is  more  stable  in  the  germline  compared  to  in  the  soma  and  in  later  embryonic  stages  compared  to  in  earlier  stages.  This  work  suggests  that  differential  mRNA  decay  across  cell  states  and  time  helps  to  shape  developmental  gene  expression,  and  it  provides  a  valuable  resource  for  studies  of  mRNA  turnover  regulatory  mechanisms.
■590    ▼aSchool  code:  0175.
■650  4▼aGenetics
■650  4▼aCellular  biology
■650  4▼aMolecular  biology
■650  4▼aDevelopmental  biology
■653    ▼amRNA  decay
■653    ▼aDevelopmental  stages
■653    ▼aEmbryogenesis
■653    ▼aEmbryonic  development
■653    ▼aCell  types
■690    ▼a0369
■690    ▼a0379
■690    ▼a0758
■690    ▼a0307
■71020▼aUniversity  of  Pennsylvania▼bCell  and  Molecular  Biology.
■7730  ▼tDissertations  Abstracts  International▼g86-02B.
■790    ▼a0175
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17162719▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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