Scientific Publications

Systematic dissection and optimization of inducible enhancers in human cells using a massively parallel reporter assay.

Publication TypeJournal Article
AuthorsMelnikov, A., Murugan A., Zhang X., Tesileanu T., Wang L., Rogov P., Feizi S., Gnirke A., Callan CG Jr, Kinney JB, Kellis M., Lander E. S., and Mikkelsen TS
AbstractLearning to read and write the transcriptional regulatory code is of central importance to progress in genetic analysis and engineering. Here we describe a massively parallel reporter assay (MPRA) that facilitates the systematic dissection of transcriptional regulatory elements. In MPRA, microarray-synthesized DNA regulatory elements and unique sequence tags are cloned into plasmids to generate a library of reporter constructs. These constructs are transfected into cells and tag expression is assayed by high-throughput sequencing. We apply MPRA to compare >27,000 variants of two inducible enhancers in human cells: a synthetic cAMP-regulated enhancer and the virus-inducible interferon-β enhancer. We first show that the resulting data define accurate maps of functional transcription factor binding sites in both enhancers at single-nucleotide resolution. We then use the data to train quantitative sequence-activity models (QSAMs) of the two enhancers. We show that QSAMs from two cellular states can be combined to design enhancer variants that optimize potentially conflicting objectives, such as maximizing induced activity while minimizing basal activity.
Year of Publication2012
JournalNature biotechnology
Volume30
Issue3
Pages271-7
Date Published (YYYY/MM/DD)2012/02/26
ISSN Number1087-0156
DOI10.1038/nbt.2137
PubMedhttp://www.ncbi.nlm.nih.gov/pubmed/22371084?dopt=Abstract