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Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome

机译:远程进化限制揭示了人类X染色体上的顺式调控相互作用

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摘要

Enhancers can regulate the transcription of genes over long genomic distances. This is thought to lead to selection against genomic rearrangements within such regions that may disrupt this functional linkage. Here we test this concept experimentally using the human X chromosome. We describe a scoring method to identify evolutionary maintenance of linkage between conserved noncoding elements and neighbouring genes. Chromatin marks associated with enhancer function are strongly correlated with this linkage score. We test > 1,000 putative enhancers by transgenesis assays in zebrafish to ascertain the identity of the target gene. The majority of active enhancers drive a transgenic expression in a pattern consistent with the known expression of a linked gene. These results show that evolutionary maintenance of linkage is a reliable predictor of an enhancer's function, and provide new information to discover the genetic basis of diseases caused by the mis-regulation of gene expression.
机译:增强子可以调节长基因组距离内基因的转录。认为这导致针对此类区域内的基因组重排的选择,这可能破坏该功能性连接。在这里,我们使用人类X染色体实验性地测试了这一概念。我们描述了一种评分方法,以确定保守的非编码元素和邻近基因之间的联系进化进化维持。与增强子功能相关的染色质标记与该连锁评分高度相关。我们通过转基因实验在斑马鱼中测试了> 1,000种推定的增强子,以确定靶基因的身份。大部分活性增强剂以与连锁基因的已知表达一致的模式驱动转基因表达。这些结果表明,连锁的进化维持是增强子功能的可靠预测因子,并提供了新的信息来发现由基因表达调控异常引起的疾病的遗传基础。

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