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DESCRIPTION (provided by applicant): DNA replication in metazoan cells has been one of the most important areas of research in biology. Even though great progress has been made in characterizing the proteins involved in this process and the regulatory circuitry evolved to ensure the fidelity of replication, there are still many fundamentally important questions that have not yet been fully understood about these specialized regions in the eukaryotic genome. One of these is the selection and maintenance of active replication start sites in complex initiation zones found at most metazoan replication origins. In this project, we propose to apply two single molecule techniques, atomic force microscopy and DNA mapping with molecular combing, to directly examine the details of DNA replication at the B-globin locus from individual human cells as a model system. Specifically, we wish (1) to determine whether multiple start sites in the initiation zone at the B-globin locus could be utilized simultaneously in a given S-phase, thus, to determine if a mechanism similar to "origin interference" found in yeast should also apply to other higher eukaryotes as a general principle of replication initiation; (2) to discover whether a specific start site used in one cell cycle could be "memorized" in subsequent S-phases, thus, to determine if an active start site could be maintained by an epigenetic mechanism; (3) to further correlate these studies with the distribution of selected chromosomal proteins in the vicinity of these loci using ChIP and optical mapping on combed DNA at high spatial resolution, thus, to determine if any of the known chromatin structural proteins can be directly linked to the selection and maintenance of active replication start sites. With these studies, not only do we wish to reveal critical insights on the nature and utility of complex replication origins, but also to further establish these single molecule methods for the study of DNA replication in individual eukaryotic cells. When such methods are combined with other established techniques, we will be able to further unravel various molecular determinants and the fundamental principles of genomic replication that should also have practical implications.
期刊论文(3)
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DOI: 10.4049/jimmunol.1000203
发表时间: 2010-05-01
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者: [Czajkowsky DM, Salanti A, Ditlev SB, Shao Z, Ghumra A, Rowe JA, Pleass RJ]
通讯作者: Pleass RJ
Feasibility: Non-Contact Cryo-Atomic Force Microscope High Resolution Bioimaging
  • 批准号:
    7683997
  • 项目类别:
  • 资助金额:
    $10.94万
  • 财政年份:
    2007
  • 负责人:
    ZHIFENG SHAO
  • 依托单位:
Feasibility: Non-Contact Cryo-Atomic Force Microscope High Resolution Bioimaging
  • 批准号:
    7491678
  • 项目类别:
  • 资助金额:
    $18.94万
  • 财政年份:
    2007
  • 负责人:
    ZHIFENG SHAO
  • 依托单位:
Feasibility: Non-Contact Cryo-Atomic Force Microscope High Resolution Bioimaging
  • 批准号:
    7024182
  • 项目类别:
  • 资助金额:
    $18.94万
  • 财政年份:
    2007
  • 负责人:
    ZHIFENG SHAO
  • 依托单位:
Genomic Mapping of Replication Origins in Higher Eukaryotes by Okazaki Analysis
  • 批准号:
    7140232
  • 项目类别:
  • 资助金额:
    $14.79万
  • 财政年份:
    2005
  • 负责人:
    ZHIFENG SHAO
  • 依托单位:
国内基金
海外基金
层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
  • 批准号:
    2021JJ40433
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2021
  • 负责人:
    孙磊
  • 依托单位:
寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
  • 批准号:
    32001603
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2020
  • 负责人:
    段真珍
  • 依托单位:
AREA国际经济模型的移植.改进和应用
  • 批准号:
    18870435
  • 项目类别:
    面上项目
  • 资助金额:
    2.0万元
  • 批准年份:
    1988
  • 负责人:
    史树中
  • 依托单位: