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Somatic Loss of Maternal POLA2 Cause...
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Lin, Alex Y.
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Somatic Loss of Maternal POLA2 Causes Tissue-dependent Cell Death and DNA Damage in POLA2 Mutant Zebrafish.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Somatic Loss of Maternal POLA2 Causes Tissue-dependent Cell Death and DNA Damage in POLA2 Mutant Zebrafish./
作者:
Lin, Alex Y.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2019,
面頁冊數:
150 p.
附註:
Source: Dissertations Abstracts International, Volume: 80-12, Section: B.
Contained By:
Dissertations Abstracts International80-12B.
標題:
Molecular biology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=13917934
ISBN:
9781392318676
Somatic Loss of Maternal POLA2 Causes Tissue-dependent Cell Death and DNA Damage in POLA2 Mutant Zebrafish.
Lin, Alex Y.
Somatic Loss of Maternal POLA2 Causes Tissue-dependent Cell Death and DNA Damage in POLA2 Mutant Zebrafish.
- Ann Arbor : ProQuest Dissertations & Theses, 2019 - 150 p.
Source: Dissertations Abstracts International, Volume: 80-12, Section: B.
Thesis (Ph.D.)--The Pennsylvania State University, 2019.
DNA replication is essential to all life. Loss of function mutations of POLA2, a critical component of DNA replication, in Saccharomyces cerevisiae and Arabidopsis thaliana causes rapid growth arrest. Due to the unicellular nature of S. cerevisiae and embryonic lethality in A. thaliana beyond the 2-cell stage, cell type-dependent effects of somatic deficiency of POLA2 on cell morphology and cellular functions have not been well elucidated. A zebrafish genetic screen for mutations that cause nuclear atypia yielded a mutant, huli hutu (hht), with a pleiotropic phenotype that included nuclear atypia in gastrointestinal cells, apoptotic nuclear fragmentation in the neurons of the brain and eyes, reduced head and eye size, and dorsal curvature of the body. The causative frameshift mutation in pola2, which encodes subunit B of DNA polymerase α (Pol α), results in a premature stop codon at the 38th amino acid position of the 600-amino acid protein. Cell cycle and DNA synthesis analyses indicated that loss of pola2 significantly increased the proportion of cells in S-phase and reduced DNA synthesis in hht larvae. DNA damage and cell death were localized to neuronal cells of the brain, eyes, and spinal cord of the hht mutants. The observation of these phenotypes were possible due to the extended 5-7 day survival of the hht fish, which stands in striking contrast with the lethality of the corresponding mutants in yeast and Arabidopsis. Our data suggest this difference is likely explained by the presence of wild-type maternal pola2 in homozygous mutant embryos that supports active DNA synthesis during early embryogenesis. The subsequent depletion of wild-type pola2 leads to defective DNA synthesis, DNA damage, cell death, and cell cycle arrest that result in the tissue-dependent cytological deformities observed in hht.
ISBN: 9781392318676Subjects--Topical Terms:
517296
Molecular biology.
Somatic Loss of Maternal POLA2 Causes Tissue-dependent Cell Death and DNA Damage in POLA2 Mutant Zebrafish.
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DNA replication is essential to all life. Loss of function mutations of POLA2, a critical component of DNA replication, in Saccharomyces cerevisiae and Arabidopsis thaliana causes rapid growth arrest. Due to the unicellular nature of S. cerevisiae and embryonic lethality in A. thaliana beyond the 2-cell stage, cell type-dependent effects of somatic deficiency of POLA2 on cell morphology and cellular functions have not been well elucidated. A zebrafish genetic screen for mutations that cause nuclear atypia yielded a mutant, huli hutu (hht), with a pleiotropic phenotype that included nuclear atypia in gastrointestinal cells, apoptotic nuclear fragmentation in the neurons of the brain and eyes, reduced head and eye size, and dorsal curvature of the body. The causative frameshift mutation in pola2, which encodes subunit B of DNA polymerase α (Pol α), results in a premature stop codon at the 38th amino acid position of the 600-amino acid protein. Cell cycle and DNA synthesis analyses indicated that loss of pola2 significantly increased the proportion of cells in S-phase and reduced DNA synthesis in hht larvae. DNA damage and cell death were localized to neuronal cells of the brain, eyes, and spinal cord of the hht mutants. The observation of these phenotypes were possible due to the extended 5-7 day survival of the hht fish, which stands in striking contrast with the lethality of the corresponding mutants in yeast and Arabidopsis. Our data suggest this difference is likely explained by the presence of wild-type maternal pola2 in homozygous mutant embryos that supports active DNA synthesis during early embryogenesis. The subsequent depletion of wild-type pola2 leads to defective DNA synthesis, DNA damage, cell death, and cell cycle arrest that result in the tissue-dependent cytological deformities observed in hht.
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