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  1. Thesis
  2. Year of 2025

CREB Mediated Hypoxia Response in Nematostella vectensis

https://doi.org/10.15102/0002001097
https://doi.org/10.15102/0002001097
ee95822b-99be-44e0-ab46-2cc5cb878efa
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QamarShaguftaFulltext.pdf QamarShaguftaFulltext.pdf (56.1 MB)
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QamarShaguftaExamAbstract.pdf QamarShaguftaExamAbstract.pdf (64 KB)
QamarShaguftaSummary.pdf QamarShaguftaSummary.pdf (94 KB)
Item type デフォルトアイテムタイプ(フル)(1)
PubDate 2026-01-30
Title
Title ネマトステラにおけるCREB依存的低酸素応答
Language ja
Title
Title CREB Mediated Hypoxia Response in Nematostella vectensis
Language en
Creator Qamar, Shagufta

× Qamar, Shagufta

en Qamar, Shagufta

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Access Rights
Access Rights open access
Access Rights URI http://purl.org/coar/access_right/c_abf2
Rights
Rights © 2025 The Author.
Rights
Rights Resource https://creativecommons.org/licenses/by-nc/4.0/
Rights Creative Commons Attribution-NonCommercial 4.0 International
Subject
Subject Scheme Other
Subject Cnidaria | transcriptome | possible link between rising oxygen levels and early metazoan evolution
Description
Description Type Abstract
Description Oxygen availability is hypothesised as one of the critical drivers of metazoan evolution and diversification. The earliest metazoans likely emerged in shallow marine shelves in the Neoproterozoic era, a period characterised by a fluctuating and spatially heterogenous redox environment. This would have imposed physiological constraints on the early animals, selecting for oxygen-responsive and stress-adaptive traits. Understanding how ancestral metazoans navigated these dynamic oxygen landscapes is therefore essential for reconstructing the evolutionary backdrop of the emergence of animal life on Earth. To investigate these mechanisms, the cnidarian Nematostella vectensis, a representative of early-diverging metazoans, is used to comprehensively investigate the molecular and developmental responses to hypoxia stress.
N. vectensis embryogenesis is demonstrated to be oxygen-dependent, with hypoxia inducing a reversible developmental arrest. Transcriptomic profiling reveals an upregulation of cAMP-response element-binding (CREB) family genes and enrichment of CREB signalling pathways under hypoxia. Targeted knockdown of key CREB homologues, followed by hypoxia culture, reveals that CREB activity is essential for coordinating the embryonic response to low oxygen: CREB activation under hypoxia induces the reversible developmental arrest, whereas loss of CREB allows embryos to aberrantly bypass this arrest, producing irreversible defects in endoderm specification. Transcriptomic profiling of CREB knockdown embryos highlights a core CREB-regulated hypoxia-response network enriched for genes involved in extracellular matrix organization, cell–cell adhesion, and tissue architecture. Comparative analysis shows that this CREB-regulated network is deeply conserved across metazoans and non-metazoan lineages.
Together, these findings position CREB as an ancient integrator that couples environmental oxygen availability to morphogenetic events, enhancing developmental robustness during early animal evolution in the fluctuating redox landscapes in Earth’s history.
Language en
Resource Type
Resource Type Identifier http://purl.org/coar/resource_type/c_db06
Resource Type doctoral thesis
Version Type
Version Type VoR
Version Type Resource http://purl.org/coar/version/c_970fb48d4fbd8a85
Identifier Registration
Identifier Registration 10.15102/0002001097
Identifier Registration Type JaLC
Dissertation Number
Dissertation Number 甲第217号
Degree Name
Language en
Degree Name Doctor of Philosophy
Date Granted
Date Granted 2025-11-30
Degree Grantor
Degree Grantor Name Identifier Scheme kakenhi
Degree Grantor Name Identifier 38005
Language en
Degree Grantor Name Okinawa Institute of Science and Technology Graduate University
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