在内在无序的转录激活域中,在没有维护氨基酸序列的情况下维护功能
Claire LeBlanc1,2, Jordan Stefani1,2, Melvin Soriano1,2
1Department of Molecular and Cell Biology, University of California Berkeley, Berkeley, 94720.
bioRxiv : the preprint server for biology
|December 16, 2024
概括
内在无序的蛋白质区域 (IDRs) 保持功能,尽管有快速的序列变化. 关键残留物的进化周转允许在灵活的IDR中进行功能性保存,例如Gcn4激活域.
科学领域:
- 进化生物学是进化的生物学.
- 分子生物学分子生物学
- 遗传学 遗传学是一种遗传学.
背景情况:
- 蛋白质的功能往往比序列更保守,特别是在折叠的域中.
- 内在无序的蛋白质区域 (IDR) 缺乏稳定的结构,使其功能性保护机制不清楚.
- 转录激活域是IDR,对基因调节至关重要.
研究的目的:
- 研究如何在内在无序的蛋白质区域 (IDR) 中保持功能,这些蛋白质区域在氨基酸序列中迅速分离.
- 探索转录激活域的进化动态,作为IDR进化的模型.
主要方法:
- 在6亿年的真菌进化过程中,系统识别了502个正统的Gcn4转录激活域.
- 在这些领域内对序列分离和功能保存进行比较分析.
主要成果:
- 尽管有显著的序列分歧,但Gcn4的中央激活域显示出强大的功能保护.
- 功能保存是通过关键的酸性和芳香性残留物的进化收益和损失来实现的.
- 激活域的交互接口的物理灵活性与其进化序列的灵活性相关.
结论:
- 简短的功能元素的快速序列循环,包括单个氨基酸,是保护内在无序蛋白区域 (IDR) 功能的一个关键机制.
- IDRs中的物理灵活性可能促进进化的可塑性,使其在保持功能的同时能够适应.
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