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Characterizing the Role of ice1 in M...
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D'Amata, Cassandra Marie.
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Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells./
作者:
D'Amata, Cassandra Marie.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2017,
面頁冊數:
95 p.
附註:
Source: Masters Abstracts International, Volume: 57-02.
Contained By:
Masters Abstracts International57-02(E).
標題:
Cellular biology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10637149
ISBN:
9780355449556
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
D'Amata, Cassandra Marie.
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
- Ann Arbor : ProQuest Dissertations & Theses, 2017 - 95 p.
Source: Masters Abstracts International, Volume: 57-02.
Thesis (M.Sc.)--University of Toronto (Canada), 2017.
Maintenance of neural stem cell (NSC) niches is required for the continued growth of the zebrafish retina and forebrain after embryogenesis. The zebrafish mutant kess564, which maps to the ice1 locus, exhibits reduced NSC niches. RNA polymerase II-dependent snRNA transcription requires the little elongation complex (LEC) for which ICE1 is an essential scaffolding component. Mutant NSCs which are normally active no longer express markers of cycling cells and become apoptotic. Furthermore, quiescent NSCs of the mutant retina are unable to dedifferentiate in response to UV lesion. Whole-transcriptome analysis of ice1 mutant larvae show a decrease in CNS and cell cycle levels, and an increase in splicing genes indicative of a possible compensatory mechanism. snRNA transcript levels appear to be unaffected in a subset of NSCs but reduced in differentiated neurons. This work demonstrates that ice1 is essential for NSC maintenance in an in vivo loss of function model.
ISBN: 9780355449556Subjects--Topical Terms:
3172791
Cellular biology.
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
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Maintenance of neural stem cell (NSC) niches is required for the continued growth of the zebrafish retina and forebrain after embryogenesis. The zebrafish mutant kess564, which maps to the ice1 locus, exhibits reduced NSC niches. RNA polymerase II-dependent snRNA transcription requires the little elongation complex (LEC) for which ICE1 is an essential scaffolding component. Mutant NSCs which are normally active no longer express markers of cycling cells and become apoptotic. Furthermore, quiescent NSCs of the mutant retina are unable to dedifferentiate in response to UV lesion. Whole-transcriptome analysis of ice1 mutant larvae show a decrease in CNS and cell cycle levels, and an increase in splicing genes indicative of a possible compensatory mechanism. snRNA transcript levels appear to be unaffected in a subset of NSCs but reduced in differentiated neurons. This work demonstrates that ice1 is essential for NSC maintenance in an in vivo loss of function model.
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