國立高雄大學圖資館 |

登入

回首頁

Investigation of Cell-Cycle Entry and DNA Replication Termination Using Single-Cell Microscopy.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Investigation of Cell-Cycle Entry and DNA Replication Termination Using Single-Cell Microscopy.
作者:	Fan, Yilin.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, 2021
面頁冊數:	152 p.
附註:	Source: Dissertations Abstracts International, Volume: 83-05, Section: B.
附註:	Advisor: Ferrell, James;Meyer, Tobias.
Contained By:	Dissertations Abstracts International83-05B.
標題:	Daughters.
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28812955
ISBN:	9798494453662

Investigation of Cell-Cycle Entry and DNA Replication Termination Using Single-Cell Microscopy.
Fan, Yilin.

Investigation of Cell-Cycle Entry and DNA Replication Termination Using Single-Cell Microscopy. - Ann Arbor : ProQuest Dissertations & Theses, 2021 - 152 p.

Source: Dissertations Abstracts International, Volume: 83-05, Section: B.

Thesis (Ph.D.)--Stanford University, 2021.

This item must not be sold to any third party vendors.

The cell cycle is a highly orchestrated series of cellular events that results in the duplication of DNA and division into two daughter cells. As a critical process during tissue development and homeostasis, the cell cycle is tightly regulated at the cellular, tissue, and organismal levels. In this thesis, we study two cellular processes that are key to cell-cycle regulation: the decision to enter the cell cycle in response to extracellular signals, and the multi-step process that replicates DNA. In the first study, we find that the decision of a newborn cell to proliferate or become quiescent is controlled by the memory of local cell density that is inherited from its mother cell. This memory regulates the expression of the cell-cycle activator cyclin D1 and inhibitor p27. Cyclin D1 and p27 form an activator-inhibitor balance in newborn cells that regulates the proliferation-quiescence decision in a sharp, ultrasensitive manner. We further show that competing cell density and mitogen signals are funneled into the cyclin D1-p27 balance through ERK signaling. We propose that memory of cell density, coupled to tight regulation of proliferation by the activator- inhibitor balance, may contribute to robust control of cell density and tissue homeostasis. In the second study, we demonstrate that replisome disassembly, a final step during DNA replication that is generally thought to be functionally downstream of nascent DNA synthesis, is continuously required for efficient DNA synthesis. Failure to disassemble replisomes traps essential replisome components on chromatin, which prevents their recycling into the soluble pool and blocks replication initiation. Cells with defects in replisome disassembly experience slow and incomplete DNA replication, G2/M checkpoint activation, and cell-cycle arrest. We also show that LRR1, which encodes a key component of the E3 ligase CRL2-LRR1 that initiates replisome disassembly, is an essential gene in actively dividing human cells. Thus we propose that inhibiting CRL2-LRR1 activity may be a potential target for cancer therapy, which acts by blocking the recycling of key replication factors that are in high demand in cancer cells due to the higher replicative activity in many cancers.

ISBN: 9798494453662Subjects--Topical Terms:

915859
Daughters.

Investigation of Cell-Cycle Entry and DNA Replication Termination Using Single-Cell Microscopy.
LDR:03386nmm a2200361 4500 001 616493
005 20220513114352.5
008 220920s2021 ||||||||||||||||| ||eng d
020 $a 9798494453662
035 $a (MiAaPQ)AAI28812955
035 $a (MiAaPQ)STANFORDzm982wf9873
035 $a AAI28812955
040 $a MiAaPQ $c MiAaPQ
100 1 $a Fan, Yilin. $3 915858
245 1 0 $a Investigation of Cell-Cycle Entry and DNA Replication Termination Using Single-Cell Microscopy.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2021
300 $a 152 p.
500 $a Source: Dissertations Abstracts International, Volume: 83-05, Section: B.
500 $a Advisor: Ferrell, James;Meyer, Tobias.
502 $a Thesis (Ph.D.)--Stanford University, 2021.
506 $a This item must not be sold to any third party vendors.
520 $a The cell cycle is a highly orchestrated series of cellular events that results in the duplication of DNA and division into two daughter cells. As a critical process during tissue development and homeostasis, the cell cycle is tightly regulated at the cellular, tissue, and organismal levels. In this thesis, we study two cellular processes that are key to cell-cycle regulation: the decision to enter the cell cycle in response to extracellular signals, and the multi-step process that replicates DNA. In the first study, we find that the decision of a newborn cell to proliferate or become quiescent is controlled by the memory of local cell density that is inherited from its mother cell. This memory regulates the expression of the cell-cycle activator cyclin D1 and inhibitor p27. Cyclin D1 and p27 form an activator-inhibitor balance in newborn cells that regulates the proliferation-quiescence decision in a sharp, ultrasensitive manner. We further show that competing cell density and mitogen signals are funneled into the cyclin D1-p27 balance through ERK signaling. We propose that memory of cell density, coupled to tight regulation of proliferation by the activator- inhibitor balance, may contribute to robust control of cell density and tissue homeostasis. In the second study, we demonstrate that replisome disassembly, a final step during DNA replication that is generally thought to be functionally downstream of nascent DNA synthesis, is continuously required for efficient DNA synthesis. Failure to disassemble replisomes traps essential replisome components on chromatin, which prevents their recycling into the soluble pool and blocks replication initiation. Cells with defects in replisome disassembly experience slow and incomplete DNA replication, G2/M checkpoint activation, and cell-cycle arrest. We also show that LRR1, which encodes a key component of the E3 ligase CRL2-LRR1 that initiates replisome disassembly, is an essential gene in actively dividing human cells. Thus we propose that inhibiting CRL2-LRR1 activity may be a potential target for cancer therapy, which acts by blocking the recycling of key replication factors that are in high demand in cancer cells due to the higher replicative activity in many cancers.
590 $a School code: 0212.
650 4 $a Daughters. $3 915859
650 4 $a CRISPR. $3 915860
650 4 $a Failure. $3 915861
650 4 $a Regulation. $3 915636
650 4 $a DNA damage. $3 229562
650 4 $a Cyclin-dependent kinases. $3 199303
650 4 $a Microscopy. $3 189037
650 4 $a Genetic engineering. $3 189009
650 4 $a Frogs. $3 627374
650 4 $a Genomes. $3 201972
650 4 $a Phosphorylation. $3 202958
650 4 $a Genes. $3 201304
650 4 $a Cell growth. $3 915565
650 4 $a Kinases. $3 915567
650 4 $a Mothers. $3 622670
650 4 $a Cell cycle. $3 193777
650 4 $a Transcription factors. $3 202406
650 4 $a Cell division. $3 188931
650 4 $a Biochemistry. $3 188609
650 4 $a Bioengineering. $3 229635
650 4 $a Cellular biology. $3 708607
650 4 $a Chemistry. $3 188628
650 4 $a Engineering. $3 210888
650 4 $a Genetics. $3 189015
690 $a 0487
690 $a 0202
690 $a 0379
690 $a 0485
690 $a 0537
690 $a 0369
710 2 $a Stanford University. $3 212607
773 0 $t Dissertations Abstracts International $g 83-05B.
790 $a 0212
791 $a Ph.D.
792 $a 2021
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28812955