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When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
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相关实验视频

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Detection of Signaling Effector-Complexes Downstream of BMP4 Using in situ PLA, a Proximity Ligation Assay
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下游的核事件在布拉西诺固醇信号中.

Grégory Vert1, Joanne Chory

  • 1Plant Biology Laboratory, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.

Nature
|May 5, 2006
PubMed
概括

铜类固醇 (BRs) 通过涉及BIN2激酶的途径调节植物生长. 新发现表明,BIN2通过酸化直接抑制核中的BES1转录因子活性,影响DNA结合.

科学领域:

  • 植物生物学 植物生物学
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 铜类固醇 (BRs) 是关键的植物类固醇激素,调节生长和发育.
  • 这种BR信号通路涉及BRI1受体,BIN2激酶和BSU1酸酶.
  • 之前的模型表明BIN2控制BES1/BZR1的稳定性和定位.

研究的目的:

  • 阐明BIN2激酶调节BR信号通路的精确机制.
  • 研究BIN2在调节BES1转录因子活性中的作用.

主要方法:

  • 研究了BES1.1的亚细胞局部化.
  • 分析了BIN2激酶对核中的BES1活性的影响.
  • 评估了BES1的BIN2介导酸化及其对DNA结合和转录活性的影响.

主要成果:

  • BES1 构成性地定位在核中.
  • 核局部化的BIN2酸化BES1,抑制其DNA结合和转录活性.
  • 酸化损害了BES1的多元化,导致转激活减少.

结论:

  • 通过酸化,BIN2激酶通过酸化直接抑制核内BES1的活动.

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  • 对DNA结合和转激活的酸化依赖抑制是BES1的主要调节机制.
  • 这项研究完善了对植物中BR信号通路调节的理解.