端粒长度稳态是通过端粒酶可扩展和不可扩展状态之间的切换来实现的
M Teresa Teixeira1, Milica Arneric, Peter Sperisen
1Swiss Institute for Experimental Cancer Research and National Center of Competence in Research Frontiers in Genetics, CH-1066 Epalinges/s Lausanne, Switzerland.
Cell
|April 28, 2004
概括
端粒长度稳态是由端粒酶维持的,它在染色体末端不均地添加核酸. 这项研究表明,端粒酶更喜欢较短的端粒,其中Rif1/Rif2蛋白控制延长频率.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 细胞生物学 细胞生物学
背景情况:
- 端粒侵蚀是由于DNA复制和核分解处理不完整而发生的.
- 了解端粒长度恒常是至关重要的,但由于缺乏对单分子端粒延长事件的测试而受到限制.
研究的目的:
- 在Saccharomyces cerevisiae中测量核酸分辨率时的端粒延长.
- 阐明控制端粒长度恒常的机制.
主要方法:
- 在Saccharomyces cerevisiae中对端粒延长的单分子分析.
- 测量端粒延伸事件的核酸分辨率测量.
主要成果:
- 每个细胞周期的端粒延长从几到100多个核酸变化,独立于端粒长度.
- 端粒酶表现出较短的端粒的优先延长.
- 删除Rif1或Rif2蛋白质通过增强延长频率来增加端粒长度.
结论:
- 端粒长度稳态由端粒酶可扩展和不可扩展状态之间的切换来调节.
- 端粒长度由端粒酶作用的频率和程度动态控制.
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