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A STUDY OF TRANSVECTION AT THE DROSOPHILA YELLOW GENE

A STUDY OF TRANSVECTION AT THE DROSOPHILA YELLOW GENE
果蝇黄色基因转染的研究
批准号:
6636514
负责人:
CHAO-TING WU
金额:
$44.65万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-07-01 至 2005-06-30

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中文摘要
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英文摘要
The proposed research explores gene regulation at the level of chromatin structure in Drosophila by focusing on transvection, an unusual form of gene modulation that reflects the proximity of a gene to its homologue. It addresses transvection at the yellow gene. Here, transvection is the basis for intragenic complementation. In particular, studies indicate that when certain alleles are paired, the enhancers of one can act in trans on the promoter of the other. The data also suggest that a prerequisite for the release of an enhancer to act in trans may be the disabling of its own promoter. The preliminary studies have expanded considerably upon this model. In addition, they suggest a second mode of transvection in which the pairing of dissimilar alleles leads to gene topologies that allow an enhancer to bypass a chromatin insulator. The proposed research tests and extends these surprising and new interpretations of transvection at yellow. Specific Aim 1 tests the model in which enhancer action in trans is controlled by the transcriptional competence of the promoter. Specific Aim 2 tests the proposal that pairing can dictate gene topologies to allow an enhancer to bypass an insulator. In Specific Aim 3, the studies extend beyond yellow and ask whether genes and the genome are generally permissiveness for transvection. Finally, Specific Aim 4 searches for the trans- acting factors that mediate and control transvection. Our studies use two technologies to meet the requirement of transvection for homologue pairing. These are targeted gene conversion (Specific Aims 1, 2, and 3) and a technique that allows the placement of genes into allelic positions on different chromosomes (Specific Aim 3). Specific Aim 4 uses standard genetic and molecular biological approaches. There is strong evidence that homologue pairing is a potent force that can cause severe consequences in many organisms. It may underlie some medical diseases and limit certain agricultural technologies. Therefore, the studies here are likely to benefit human welfare through contributions to both medicine and agriculture.
期刊论文(17)
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会议论文
Scalable amplification of strand subsets from chip-synthesized oligonucleotide libraries.
从芯片合成的寡核苷酸文库中可扩展地扩增链子集。
DOI: 10.1038/ncomms9634
发表时间: 2015-11-16
期刊: Nature communications
影响因子: 16.6
作者: [Schmidt TL, Beliveau BJ, Uca YO, Theilmann M, Da Cruz F, Wu CT, Shih WM]
通讯作者: Shih WM
DOI: 10.1371/journal.pgen.1002667
发表时间: 2012
期刊: PLoS genetics
影响因子: 4.5
作者: [Joyce EF, Williams BR, Xie T, Wu CT]
通讯作者: Wu CT
DOI: 10.1371/journal.pgen.1004646
发表时间: 2014-10
期刊: PLoS genetics
影响因子: 4.5
作者: [McCole RB, Fonseka CY, Koren A, Wu CT]
通讯作者: Wu CT
Does random X-inactivation in mammals reflect a random choice between two X chromosomes?
哺乳动物中随机 X 失活是否反映了两条 X 染色体之间的随机选择?
DOI: 10.1534/genetics.104.029819
发表时间: 2004
期刊: Genetics.
影响因子: --
作者: [Williams,BenjaminR, Wu,Chao-Ting]
通讯作者: Wu,Chao-Ting
7
    Center for Genome Imaging
    • 批准号:
      10421292
    • 项目类别:
    • 资助金额:
      $250.0万
    • 财政年份:
      2021
    • 负责人:
      CHAO-TING WU
    • 依托单位:
    Center for Genome Imaging
    • 批准号:
      10177498
    • 项目类别:
    • 资助金额:
      $324.82万
    • 财政年份:
      2021
    • 负责人:
      CHAO-TING WU
    • 依托单位:
    Center for Genome Imaging
    • 批准号:
      10597684
    • 项目类别:
    • 资助金额:
      $250.0万
    • 财政年份:
      2021
    • 负责人:
      CHAO-TING WU
    • 依托单位:
    Technologies for visualizing the genome in situ
    • 批准号:
      9290042
    • 项目类别:
    • 资助金额:
      $62.19万
    • 财政年份:
      2017
    • 负责人:
      CHAO-TING WU
    • 依托单位:
    海外基金