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Control of Early Germline Development in C. elegans

Control of Early Germline Development in C. elegans
线虫早期种系发育的控制
批准号:
7069974
负责人:
Susan Strome
金额:
$42.58万
依托单位国家:
美国
项目类别:
财政年份:
1984
资助国家:
美国
项目状态:
已结题
起止时间:
1984-09-01 至 2007-06-30

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中文摘要
翻译
描述(由申请人提供):生殖细胞负责物种的繁殖和延续,因此在发育中起着关键作用。我们正在研究保存生殖细胞不朽的机制,并在秀丽隐杆线虫模型系统中使用遗传学,基因组学,分子和生化方法的组合来指导它们独特的发育程序。我们之前鉴定了四种秀丽隐杆线虫MES蛋白是生殖细胞不朽所必需的。MES-2、MES-3和MES-6构成了蠕虫染色质调控的Polycomb Group,作为一个复合体运作,参与维持X染色体在大多数种系发育过程中的沉默状态。MES-4与常染色体结合,可能起到保护常染色体免于沉默的作用。MES系统在染色质中组蛋白尾部的修饰水平上运行。MES-2/3/6复合物催化组蛋白H3 Lys27的甲基化,从而抑制基因表达。本建议的目标是:a)阐明MES-3和MES-6以及可能的MES-6的替代伙伴如何通过MES-2影响组蛋白甲基化,b)验证我们的预测,即MES-4也起甲基化组蛋白的作用,并识别与MES-4一起作用的其他蛋白质,c)研究MES-4如何特异性靶向常染色体,d)识别一些表达受MES-2/3/6和MES-4调节的基因。e)确定MES- 2/3/6和MES-4如何相互连接并与SynMuv类染色质调节因子连接。染色质组织的动态调控是控制基因表达和发育的关键水平,而调控不当已知会导致疾病状态和癌症。我们的研究将对理解生殖细胞中染色质状态的控制、常染色体和性染色体的区分机制以及特定的染色质需求做出重要贡献。
英文摘要
DESCRIPTION (provided by applicant): Germ cells are responsible for the fertility and perpetuation of species and thus serve a key role in development. We are investigating the mechanisms that preserve the immortality of germ cells and guide their unique developmental program, using a combination of genetics, genomics, and molecular and biochemical approaches in the model system Caenorhabditis elegans. We previously identified four C. elegans MES proteins as being required for germ cell immortality. MES-2, MES-3, and MES-6 constitute the Polycomb Group of chromatin regulators in worms, operate as a complex, and participate in maintaining the X chromosomes in a silenced state throughout most of germline development. MES-4 binds the autosomes and may function to protect them from silencing. The MES system operates at the level of modification of histone tails in chromatin. The MES-2/3/6 complex catalyzes methylation of histone H3 Lys27, which represses gene expression. The goals of this proposal are to: a) elucidate how MES-3 and MES-6 and perhaps an alternative partner to MES-6 influence histone methylation by MES-2, b) test our prediction that MES-4 also functions to methylate histones and identify other proteins that operate with MES-4, c) investigate how MES-4 is targeted specifically to the autosomes, d) identify some of the genes whose expression is regulated by MES-2/3/6 and MES-4, and e) determine how MES- 2/3/6 and MES-4 interface with each other and with the SynMuv class of chromatin regulators. The dynamic regulation of chromatin organization is a crucial level of control of gene expression and development, and misregulation is known to contribute to disease states and cancers. Our studies will make important contributions to understanding control of chromatin states, mechanisms for discriminating between the autosomes and the sex chromosomes, and specific chromatin requirements in germ cells.
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Training Program in Molecular, Cell, and Developmental Biology
INTERNATIONAL C ELEGANS MEETING
  • 批准号:
    2807513
  • 项目类别:
  • 资助金额:
    $7.88万
  • 财政年份:
    1999
  • 负责人:
    Susan Strome
  • 依托单位:
Training Program in Molecular, Cell, and Development Biology
Training Program in Molecular, Cell, and Development Biology
海外基金