Quantitative assessment of RNA-protein interactions with high-throughput sequencing-RNA affinity profiling.

Abstract:

:Because RNA-protein interactions have a central role in a wide array of biological processes, methods that enable a quantitative assessment of these interactions in a high-throughput manner are in great demand. Recently, we developed the high-throughput sequencing-RNA affinity profiling (HiTS-RAP) assay that couples sequencing on an Illumina GAIIx genome analyzer with the quantitative assessment of protein-RNA interactions. This assay is able to analyze interactions between one or possibly several proteins with millions of different RNAs in a single experiment. We have successfully used HiTS-RAP to analyze interactions of the EGFP and negative elongation factor subunit E (NELF-E) proteins with their corresponding canonical and mutant RNA aptamers. Here we provide a detailed protocol for HiTS-RAP that can be completed in about a month (8 d hands-on time). This includes the preparation and testing of recombinant proteins and DNA templates, clustering DNA templates on a flowcell, HiTS and protein binding with a GAIIx instrument, and finally data analysis. We also highlight aspects of HiTS-RAP that can be further improved and points of comparison between HiTS-RAP and two other recently developed methods, quantitative analysis of RNA on a massively parallel array (RNA-MaP) and RNA Bind-n-Seq (RBNS), for quantitative analysis of RNA-protein interactions.

journal_name

Nat Protoc

journal_title

Nature protocols

authors

Ozer A,Tome JM,Friedman RC,Gheba D,Schroth GP,Lis JT

doi

10.1038/nprot.2015.074

subject

Has Abstract

pub_date

2015-08-01 00:00:00

pages

1212-33

issue

8

eissn

1754-2189

issn

1750-2799

pii

nprot.2015.074

journal_volume

10

pub_type

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