Inoue Fumitaka, Ahituv Nadav
Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA 94158, USA; Institute for Human Genetics, University of California San Francisco, San Francisco, CA 94158, USA.
Genomics. 2015 Sep;106(3):159-164. doi: 10.1016/j.ygeno.2015.06.005. Epub 2015 Jun 10.
Enhancers control the timing, location and expression levels of their target genes. Nucleotide variation in enhancers has been shown to lead to numerous phenotypes, including human disease. While putative enhancer sequences and nucleotide variation within them can now be detected in a rapid manner using various genomic technologies, the understanding of the functional consequences of these variants still remains largely unknown. Massively parallel reporter assays (MPRAs) can overcome this hurdle by providing the ability to test thousands of sequences and nucleotide variants within them for enhancer activity en masse. Here, we describe this technology and specifically focus on how it is being used to obtain an increased understanding of enhancer regulatory code and grammar.
增强子控制其靶基因的时间、位置和表达水平。增强子中的核苷酸变异已被证明会导致多种表型,包括人类疾病。虽然现在可以使用各种基因组技术快速检测推定的增强子序列及其内部的核苷酸变异,但对这些变异的功能后果的了解仍然知之甚少。大规模平行报告基因检测(MPRA)可以通过大规模测试数千个序列及其内部的核苷酸变异的增强子活性来克服这一障碍。在这里,我们描述了这项技术,并特别关注它如何被用于增进对增强子调控密码和语法的理解。