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Regulation of Chromatin Structure and Segregation- [electronic resource]
Contents Info
Regulation of Chromatin Structure and Segregation- [electronic resource]
자료유형  
 학위논문
Control Number  
0016934843
International Standard Book Number  
9798380335997
Dewey Decimal Classification Number  
574
Main Entry-Personal Name  
Ng, Henry.
Publication, Distribution, etc. (Imprint  
[S.l.] : University of California, San Francisco., 2023
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2023
Physical Description  
1 online resource(153 p.)
General Note  
Source: Dissertations Abstracts International, Volume: 85-03, Section: B.
General Note  
Advisor: Johnson, Alexander;Al-Sady, Bassem.
Dissertation Note  
Thesis (Ph.D.)--University of California, San Francisco, 2023.
Restrictions on Access Note  
This item must not be sold to any third party vendors.
Summary, Etc.  
요약The genetic material is packaged differentially at different phases of the cell cycle. In interphase, cells package their genome into heterochromatin and euchromatin domains, where genes are repressed or expressed based on cell identity. Heterochromatin, the gene-repressive structure, is regulated by different factors that control methylation and acetylation on histones. During cell division, these histone modifications are copied onto the newly synthesized DNA. The heterochromatin structure is seeded from nucleation DNA sequence that recruits other factors to spread the domain. In our studies, we found that the factors required for spreading heterochromatin in different genomic regions are highly variable. Notably, we proposed a mechanism by which Fkh2, a transcription factor, recruits Clr6 histone deacetylase complex I" to a nucleated heterochromatin domain that initiates the spread of heterochromatin domains.During mitosis, the chromatin is packaged into condensed chromosomes for faithful segregation of the duplicated genome. Progression through mitosis is regulated by the levels of a family of protein kinase complexes named Cyclin-Dependent Kinases (CDKs). The phosphorylation of numerous CDK substrates drives various mitosis events. We identified a novel phosphate-binding pocket on cyclins that aids in the timing of sequential multisite phosphorylation in CDK substrates and mitotic events. Loss of this pocket causes a mitotic delay in vivo as well as loss of multisite phosphorylation in various CDK substrates in vitro. 
Subject Added Entry-Topical Term  
Biochemistry.
Subject Added Entry-Topical Term  
Cellular biology.
Subject Added Entry-Topical Term  
Genetics.
Index Term-Uncontrolled  
Heterochromatin
Index Term-Uncontrolled  
Mitosis
Index Term-Uncontrolled  
Phosphorylation
Index Term-Uncontrolled  
Cell cycle
Index Term-Uncontrolled  
Genetic material
Added Entry-Corporate Name  
University of California, San Francisco Biochemistry and Molecular Biology
Host Item Entry  
Dissertations Abstracts International. 85-03B.
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
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Control Number  
joongbu:639243
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