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Regulation of Chromatin Structure and Segregation- [electronic resource]
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
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:639243
detalle info
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