VISTA 数据库中的验证负区 (VNR) 可能是真正增强子的截断形式

Pengyu Ni, Siwen Wu, Zhengchang Su
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引用次数: 0

摘要

VISTA 增强子数据库是评估人类和小鼠中预测增强子的宝贵资源。除了人类和小鼠基因组中数以千计的验证阳性区域(VPRs)外,该数据库还包含类似数量的验证阴性区域(VNRs)。以前的研究表明,VPRs 的平均长度是高度保守的重叠增强子预测长度的一半,并假设 VPRs 可能是长的真正增强子的截短形式。这里的研究表明,与 VPRs 一样,VNRs 也受到强烈的进化限制,并与基因组中预测的增强子重叠。与高度保守的预测重叠增强子相比,VNRs 的长度平均只有一半。此外,VNRs 和 VPRs 对活性增强子的关键表观遗传标记显示出类似的细胞/组织特异性修饰模式。此外,VNRs 和 VPRs 还显示出相似的硅突变影响得分谱。VPRs 和 VNRs 的这些高度相似的特性表明,与 VPRs 一样,VNRs 也可能是真正的长增强子的截短形式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Validated Negative Regions (VNRs) in the VISTA Database might be Truncated Forms of Bona Fide Enhancers

Validated Negative Regions (VNRs) in the VISTA Database might be Truncated Forms of Bona Fide Enhancers

The VISTA enhancer database is a valuable resource for evaluating predicted enhancers in humans and mice. In addition to thousands of validated positive regions (VPRs) in the human and mouse genomes, the database also contains similar numbers of validated negative regions (VNRs). It is previously shown that the VPRs are on average half as long as predicted overlapping enhancers that are highly conserved and hypothesize that the VPRs may be truncated forms of long bona fide enhancers. Here, it is shown that like the VPRs, the VNRs also are under strong evolutionary constraints and overlap predicted enhancers in the genomes. The VNRs are also on average half as long as predicted overlapping enhancers that are highly conserved. Moreover, the VNRs and the VPRs display similar cell/tissue-specific modification patterns of key epigenetic marks of active enhancers. Furthermore, the VNRs and the VPRs show similar impact score spectra of in silico mutagenesis. These highly similar properties between the VPRs and the VNRs suggest that like the VPRs, the VNRs may also be truncated forms of long bona fide enhancers.

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