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Multiple zebrafish atoh1 genes speci...
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Kidwell, Chelsea U.
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Multiple zebrafish atoh1 genes specify a diversity of neuronal types in the zebrafish hindbrain.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Multiple zebrafish atoh1 genes specify a diversity of neuronal types in the zebrafish hindbrain./
作者:
Kidwell, Chelsea U.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:
60 p.
附註:
Source: Dissertation Abstracts International, Volume: 78-07(E), Section: B.
Contained By:
Dissertation Abstracts International78-07B(E).
標題:
Developmental biology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10239496
ISBN:
9781369514704
Multiple zebrafish atoh1 genes specify a diversity of neuronal types in the zebrafish hindbrain.
Kidwell, Chelsea U.
Multiple zebrafish atoh1 genes specify a diversity of neuronal types in the zebrafish hindbrain.
- Ann Arbor : ProQuest Dissertations & Theses, 2016 - 60 p.
Source: Dissertation Abstracts International, Volume: 78-07(E), Section: B.
Thesis (Ph.D.)--University of Washington, 2016.
The basic Helix-Loop-Helix transcription factor, Atoh1, is known to specify several neuronal subtypes including one of most abundant cell types in the vertebrate brain, cerebellar granule neurons. The function of atoh1 in the development of cerebellar granule neurons is poorly understood. Here we use the zebrafish CNS to explore the role of atoh1 in granule neuron specification and in the generation of neuronal diversity. With the use of single and compound atoh1 mutants, we show that out of the three atoh1 genes in the zebrafish genome, atoh1c plays the most prominent role in granule neuron development but together atoh1c and atoh1a are required for the full complement of granule neurons. Interestingly, atoh1a and atoh1c specify non-overlapping granule populations, indicating that fish use multiple atoh1 genes to generate additional neuronal diversity that is not detected in mammals. In addition, we have identified a novel population of atoh1c-derived neurons closely associated with the conserved noradrenergic neurons of the Locus Coeruleus. Finally, with the use of live imaging possible in zebrafish, we discovered expression of atoh1c at the rhombic lip promotes the apical detachment of granule neuron progenitors from surrounding neuroepithelium and this process is critical for neuronal maturation. This study provides us with a better understanding of how a proneural transcription factor influences neurogenesis in the vertebrate brain.
ISBN: 9781369514704Subjects--Topical Terms:
592588
Developmental biology.
Multiple zebrafish atoh1 genes specify a diversity of neuronal types in the zebrafish hindbrain.
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The basic Helix-Loop-Helix transcription factor, Atoh1, is known to specify several neuronal subtypes including one of most abundant cell types in the vertebrate brain, cerebellar granule neurons. The function of atoh1 in the development of cerebellar granule neurons is poorly understood. Here we use the zebrafish CNS to explore the role of atoh1 in granule neuron specification and in the generation of neuronal diversity. With the use of single and compound atoh1 mutants, we show that out of the three atoh1 genes in the zebrafish genome, atoh1c plays the most prominent role in granule neuron development but together atoh1c and atoh1a are required for the full complement of granule neurons. Interestingly, atoh1a and atoh1c specify non-overlapping granule populations, indicating that fish use multiple atoh1 genes to generate additional neuronal diversity that is not detected in mammals. In addition, we have identified a novel population of atoh1c-derived neurons closely associated with the conserved noradrenergic neurons of the Locus Coeruleus. Finally, with the use of live imaging possible in zebrafish, we discovered expression of atoh1c at the rhombic lip promotes the apical detachment of granule neuron progenitors from surrounding neuroepithelium and this process is critical for neuronal maturation. This study provides us with a better understanding of how a proneural transcription factor influences neurogenesis in the vertebrate brain.
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