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RIP-Seq

Overview

Protein-RNA interactions play important roles in multiple post-transcriptional regulation processes such as RNA cleavage, transport, sequence editing, intracellular localization and translational control. RNA immunoprecipitation (RIP) can be used to detect the association of individual proteins with specific nucleic acids. RNA immunoprecipitation sequencing (RIP-Seq) is a revolutionary technology that reveals the interaction of RNA and RNA-binding proteins at the genome-wide level. RIP-Seq maps the sites at which proteins are bound to the RNA and provides single-base resolution of protein-bound RNA.

Service Specifications Demo Reports

Applications

  • Applications range from transcriptional regulation to developmental pathways to disease mechanisms and beyond.

Advantages

  • Academic Service: Novogene provides scientific service and meticulous design to guarantee high-quality research results from material selection, library preparation and sequencing, to data analysis.
  • Data Quality: Unsurpassed data quality with a guaranteed Q30 score ≥ 80% that exceeds Illumina’s official benchmarks.
  • Comprehensive Analysis: Professional bioinformatic tools enables protein binding site screening and identification from transcriptomic perspective, and invetigation of in-depth interpretation of target RNA-protein interactions.

Sample Requirements

Sample Type Required Amount Peaks Distribution Purity
Enriched RNA Sample
≥100 ng (Concentration ≥3 ng/μl)
For unfragmented sample, the main peak should be higher that 1000bp.
OD260/280>2.0
No degradation or DNA contamination

Sequencing Parameter and Analysis

Platform Type Illumina Novaseq 6000
Read Length Pair-end 150
Recommended Sequencing Depth ≥20 million read pair per sample for the species with reference genome
Standard Data Analysis
Data quality control
Mapping onto reference genome
Peak calling
Motif prediction
Peak annotation
Functional analysis of peak-associated genes
Visualization of RIP-seq data

Note: For detailed information, please refer to the Service Specifications & Demo Reports and contact us for customized requests.

Project Workflow

Sample Quality Control

Library Quality Control

Data Quality Control

Sample Preparation

Library Construction

Sequencing

Bioinformatics Analysis

The RNA binding protein SORBS2 suppresses metastatic colonization of ovarian cancer by stabilizing tumorsuppressive immunomodulatory transcripts

Background:

Ovarian cancer constitutes one of the most lethal gynecologic malignancies for females. In this study, the RNA-binding proteins (RBPs) sorbin and SH3 domain containing 2 (SORBS2) is identified as a potent suppressor of ovarian cancer metastatic colonization. Mechanistic studies show that SORBS2 binds the 3′-untranslated regions (UTRs) of WFDC1 (WAP four-disulfide core domain 1) and IL-17D (Interleukin-17D), two secreted molecules that are shown to act as metastasis suppressors. By enhancing the stability of these gene transcripts, SORBS2 suppresses ovarian cancer invasiveness and affects monocyte to myeloid-derived suppressor cell and M2-like macrophage polarization, eliciting a tumor-suppressive immune microenvironment.

Sampling & Sequencing Strategy:

2.1. Samples:
A2780s ovarian cancer cell lines

2.2. Library preparation:
RIP-seq library and RNA-seq library

2.3. Sequencing:
Illumina HiSeq, PE150

2.4. Bioinformatics analysis:
RIP-seq standard analysis and Gene expression analysis

Figure 1. Epigenetic adaptations in the anterior cingulate cortex following child abuse.

Figure 2. DNA methylation was measured in sorted populations of NeuN+ and Sox10+ nuclei, focusing on differentially methylated loci identified by RRBS.
Results:

1) Integrated analysis identifies SORBS2 as a key RBP that suppresses ovarian cancer metastasis and its expression is associated with clinical outcome of ovarian cancer patients
Through cross-referencing a list of RBPs in the published literature, public oncogenomic data analysis, and searching in the cBioPortal TCGA ovarian cancer dataset, 4 genes were identified and showed deletion in more than 5% of TCGA ovarian cancer samples (Fig. 1a, b). Only SORBS2 and MEX3D gene knock-down significantly increased the metastatic colonization capacity of ovarian cancer (Fig. 1c). Only SORBS2 was significantly correlated with overall survival of ovarian cancer patients in the Australian Ovarian Cancer Study (AOCS) dataset (GSE9891) (Fig. 1d).

2) WFDC1 and IL-17D mRNAs are bound by SORBS2 and destabilized by SORBS2 depletion
RIP sequencing was performed to identify endogenous RNA targets of SORBS2 in ovarian cancer cells (Fig. 2a). Relative transcript levels in treated SORBS2-depleted or control A2780s ovarian cancer cells were determined through transcriptomic sequencing, revealing a set of transcripts whose stability was deregulated upon SORBS2 loss. A proportion of transcripts bound by SORBS2 was found to overlap with the group of transcripts destabilized by SORBS2 knockdown compared with transcripts with no SORBS2-dependent changes in stability (Fig. 2b). Among the 91 gene transcripts potentially bound and stabilized by SORBS2, seven transcripts encoding secreted proteins attracted our attention since we focus on potential interactions between ovarian cancer cells and the tumor microenvironment during the metastatic process (Fig. 2c, d). WFDC1 and IL-17D exhibited reduced steady-state levels upon SORBS2 knockdown in both cell lines.

Conclusion:

This study takes advantage of the combination of RNA-seq and RIP-seq technology to illustrate a novel post-transcriptional network that links cancer progression and immunomodulation within the tumor microenvironment through SORBS2-mediated transcript stabilization.


Figure 1 Plots of strand cross correlation.png


Figure 2 Motif analysis.pdf


Figure 3 Enrichment analysis among samples.pdf


Figure 4 GO enrichment.png


Figure 5 KEGG enrichment scatter.png