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Spatiotemporal Coordination of Proliferation and Patterning in Early Embryonic Development
Spatiotemporal Coordination of Proliferation and Patterning in Early Embryonic Development
Spatiotemporal Coordination of Proliferation and Patterning in Early Embryonic Development

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20260202105237
ISBN  
9798291567951
DDC  
530
저자명  
Kadiyala, Usha.
서명/저자  
Spatiotemporal Coordination of Proliferation and Patterning in Early Embryonic Development
발행사항  
[Sl] : University of Michigan, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
145 p
주기사항  
Source: Dissertations Abstracts International, Volume: 87-02, Section: B.
주기사항  
Advisor: Yang, Qiong.
학위논문주기  
Thesis (Ph.D.)--University of Michigan, 2025.
초록/해제  
요약A central challenge in developmental biology is understanding how embryos coordinate cellular behaviors across space and time to transform a single cell into a structured organism. This dissertation investigates how zebrafish embryos solve this challenge through context-dependent coupling of proliferation, patterning, and mechanics during two key developmental stages: somitogenesis and early morphogenesis. During somitogenesis, the presomitic mesoderm (PSM) simultaneously proliferates and periodically segments into somites. We show that this coordination arises from spatially patterned, bidirectional coupling between the segmentation clock and the cell cycle, mediated by Notch signaling and cyclin-dependent kinases. This creates distinct functional zones where weak coupling in the posterior progenitor zone enables rapid proliferation, while strong phase-locking in the central PSM coordinates divisions with pattern formation. This oscillator coupling maintains proper somite proportions and creates tissue organization from local molecular interactions. Early morphogenesis presents a parallel coordination challenge: how do proliferation, differentiation, and mechanical forces integrate to drive autonomous tissue shape changes? Here, using zebrafish embryonic explants (pescoids) as a minimal active matter system, we reveal how cellular aggregates undergo fluid-to-solid-like and wetting to dwetting, transitions on a glass substrate. We show that the wetting phase is driven by proliferation-induced extensile forces, while the dewetting phase is mediated by mesendoderm specification and myosin II dependent contractility. This morphogenetic switch is intrinsically programmed, and we show that spatial gradients of proliferation, differentiation, and contractility create feedback loops that drive coordinated tissue-scale shape changes. Together, these studies demonstrate how zebrafish embryos achieve developmental coordination through context-dependent coupling mechanisms operating from molecular interactions to tissue-scale forces.
일반주제명  
Physics
일반주제명  
Developmental biology
일반주제명  
Biophysics
일반주제명  
Cellular biology
키워드  
Biological oscillators
키워드  
Segmentation clock
키워드  
Developmental patterning
키워드  
Embryos
키워드  
Presomitic mesoderm
기타저자  
University of Michigan Biophysics
기본자료저록  
Dissertations Abstracts International. 87-02B.
전자적 위치 및 접속  
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■020    ▼a9798291567951
■035    ▼a(MiAaPQ)AAI32271964
■035    ▼a(MiAaPQ)umichrackham006503
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a530
■1001  ▼aKadiyala,  Usha.
■24510▼aSpatiotemporal  Coordination  of  Proliferation  and  Patterning  in  Early  Embryonic  Development
■260    ▼a[Sl]▼bUniversity  of  Michigan▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a145  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  87-02,  Section:  B.
■500    ▼aAdvisor:  Yang,  Qiong.
■5021  ▼aThesis  (Ph.D.)--University  of  Michigan,  2025.
■520    ▼aA  central  challenge  in  developmental  biology  is  understanding  how  embryos  coordinate  cellular  behaviors  across  space  and  time  to  transform  a  single  cell  into  a  structured  organism.  This  dissertation  investigates  how  zebrafish  embryos  solve  this  challenge  through  context-dependent  coupling  of  proliferation,  patterning,  and  mechanics  during  two  key  developmental  stages:  somitogenesis  and  early  morphogenesis.    During  somitogenesis,  the  presomitic  mesoderm  (PSM)  simultaneously  proliferates  and  periodically  segments  into  somites.  We  show  that  this  coordination  arises  from  spatially  patterned,  bidirectional  coupling  between  the  segmentation  clock  and  the  cell  cycle,  mediated  by  Notch  signaling  and  cyclin-dependent  kinases.  This  creates  distinct  functional  zones  where  weak  coupling  in  the  posterior  progenitor  zone  enables  rapid  proliferation,  while  strong  phase-locking  in  the  central  PSM  coordinates  divisions  with  pattern  formation.  This  oscillator  coupling  maintains  proper  somite  proportions  and  creates  tissue  organization  from  local  molecular  interactions.  Early  morphogenesis  presents  a  parallel  coordination  challenge:  how  do  proliferation,  differentiation,  and  mechanical  forces  integrate  to  drive  autonomous  tissue  shape  changes?  Here,  using  zebrafish  embryonic  explants  (pescoids)  as  a  minimal  active  matter  system,  we  reveal  how  cellular  aggregates  undergo  fluid-to-solid-like  and  wetting  to  dwetting,  transitions  on  a  glass  substrate.  We  show  that  the  wetting  phase  is  driven  by  proliferation-induced  extensile  forces,  while  the  dewetting  phase  is  mediated  by  mesendoderm  specification  and  myosin  II  dependent  contractility.  This  morphogenetic  switch  is  intrinsically  programmed,  and  we  show  that  spatial  gradients  of  proliferation,  differentiation,  and  contractility  create  feedback  loops  that  drive  coordinated  tissue-scale  shape  changes.    Together,  these  studies  demonstrate  how  zebrafish  embryos  achieve  developmental  coordination  through  context-dependent  coupling  mechanisms  operating  from  molecular  interactions  to  tissue-scale  forces.
■590    ▼aSchool  code:  0127.
■650  4▼aPhysics
■650  4▼aDevelopmental  biology
■650  4▼aBiophysics
■650  4▼aCellular  biology
■653    ▼aBiological  oscillators
■653    ▼aSegmentation  clock
■653    ▼aDevelopmental  patterning
■653    ▼aEmbryos
■653    ▼aPresomitic  mesoderm
■690    ▼a0786
■690    ▼a0605
■690    ▼a0758
■690    ▼a0379
■71020▼aUniversity  of  Michigan▼bBiophysics.
■7730  ▼tDissertations  Abstracts  International▼g87-02B.
■790    ▼a0127
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17359930▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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