CHHM:一个手动策划的人类质子修饰的目录,揭示热点区域和独特的分布模式
Wendong Ma1, Xiaofan Ding1, Jiajia Xu1
1Institute of Translational Medicine, Centre for Precision Medicine Research and Training, MoE Frontiers Science Center for Precision Oncology, Faculty of Health Sciences, University of Macau, Macau, 999078, China.
一个新的人体基因组修饰 (CHHM) 编辑目录整合了分散的数据,揭示了对表观遗传控制和疾病的洞察力. CHHM为研究质子修饰和转录调节的研究人员提供了一个用户友好的资源.
科学领域:
- 表观遗传学和分子生物学
- 基因组学和蛋白质组学
背景情况:
- 基因组蛋白修饰对于表观遗传控制,调节生物过程和疾病发展至关重要.
- 现有的人类基因组修饰数据在多个数据库中分散,阻碍了全面的研究.
研究的目的:
- 创建一个统一的,精心策划的人体基因素修饰 (CHHM) 的目录.
- 为研究人员提供一个用户友好的资源,提供证据可信度水平.
- 提供对基因素修饰机制和表观遗传控制的新见解.
主要方法:
- 手动检索和整合来自10个知识库/数据库和3个文章的修改记录.
- 对6612个非冗余修改条目进行证据评估和策划.
- 包括31种修饰类型,2种基因组-DNA交叉链接,以及各种基因组变异 (H1,H2A,H2B,H3,H4) 的数据.
主要成果:
- 该CHHM目录包含6612个非冗余的人体质子修饰条目.
- 化修饰是最丰富的类型,突出显示了细胞代谢的作用.
- 基质子家族之间分布不均,表明对修饰的敏感性差异,确定了热点区域.
结论:
- CHHM是生物医学,临床和基因组蛋白修饰的基础研究的宝贵资源.
- 该目录促进了对转录调节和表观遗传机制的研究.
- 研究结果表明,细胞代谢状态和表观遗传控制之间存在显著联系.
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