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基于功能的哺乳动物增强子的鉴定,使用特定位置的整合。

Function-based identification of mammalian enhancers using site-specific integration.

机构信息

Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA.

1] Gladstone Institute of Cardiovascular Disease, San Francisco, California, USA. [2] Roddenberry Center for Stem Cell Biology and Medicine at Gladstone Institutes, San Francisco, California, USA.

出版信息

Nat Methods. 2014 May;11(5):566-71. doi: 10.1038/nmeth.2886. Epub 2014 Mar 23.

Abstract

The accurate and comprehensive identification of functional regulatory sequences in mammalian genomes remains a major challenge. Here we describe site-specific integration fluorescence-activated cell sorting followed by sequencing (SIF-seq), an unbiased, medium-throughput functional assay for the discovery of distant-acting enhancers. Targeted single-copy genomic integration into pluripotent cells, reporter assays and flow cytometry are coupled with high-throughput DNA sequencing to enable parallel screening of large numbers of DNA sequences. By functionally interrogating >500 kilobases (kb) of mouse and human sequence in mouse embryonic stem cells for enhancer activity we identified enhancers at pluripotency loci including NANOG. In in vitro-differentiated cardiomyocytes and neural progenitor cells, we identified cardiac enhancers and neuronal enhancers, respectively. SIF-seq is a powerful and flexible method for de novo functional identification of mammalian enhancers in a potentially wide variety of cell types.

摘要

哺乳动物基因组中功能调节序列的准确全面鉴定仍然是一个主要挑战。在这里,我们描述了一种无偏、中等通量的功能测定方法,即基于特异性整合的荧光激活细胞分选和测序(SIF-seq),用于发现远距离作用的增强子。通过将靶向的单拷贝基因组整合到多能细胞中,结合报告基因检测和流式细胞术,与高通量 DNA 测序相结合,可实现对大量 DNA 序列的平行筛选。通过对小鼠胚胎干细胞中超过 500 千碱基(kb)的序列进行功能分析,我们鉴定到了包括 NANOG 在内的多能性基因座的增强子。在体外分化的心肌细胞和神经祖细胞中,我们分别鉴定到了心脏增强子和神经元增强子。SIF-seq 是一种强大而灵活的方法,可在多种潜在的细胞类型中从头鉴定哺乳动物增强子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a20/4008384/1a7f2861a6c3/emss-57097-f0001.jpg

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