Item Type: | Article |
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Title: | Expanding the map of protein-RNA interaction sites via cell fusion followed by PAR-CLIP |
Creators Name: | Hinze, F., Drewe-Boss, P., Milek, M., Ohler, U., Landthaler, M. and Gotthardt, M. |
Abstract: | PAR-CLIP (photoactivatable ribonucleoside-enhanced crosslinking and immunoprecipitation) facilitates the identification and mapping of protein/RNA interactions. So far, it has been limited to select cell-lines as it requires efficient 4SU uptake. To increase transcriptome complexity and thus identify additional RNA-protein interaction sites we fused HEK 293 T-Rex cells (HEK293-Y) that express the RNA binding protein YBX1 with PC12 cells expressing eGFP (PC12-eGFP). The resulting hybrids enable PAR-CLIP on a neuronally expanded transcriptome (Fusion-CLIP) and serve as a proof of principle. The fusion cells express both parental marker genes YBX1 and eGFP and the expanded transcriptome contains human and rat transcripts. PAR-CLIP of fused cells versus the parental HEK293-Y identified 768 novel RNA targets of YBX1. We were able to trace the origin of the majority of the short PAR-CLIP reads as they differentially mapped to the human and rat genome. Furthermore, Fusion-CLIP expanded the CAUC RNA binding motif of YBX1 to UCUUUNNCAUC. The fusion of HEK293-Y and PC12-eGFP cells resulted in cells with a diverse genome expressing human and rat transcripts that enabled the identification of novel YBX1 substrates. The technique allows the expansion of the HEK 293 transcriptome and makes PAR-CLIP available to fusion cells of diverse origin. |
Keywords: | PAR-CLIP, Cell Fusion, YBX1, RNAseq, Transcriptomics, RNA Processing, RNA-Binding Protein, Animals, Rats |
Source: | RNA Biology |
ISSN: | 1547-6286 |
Publisher: | Taylor & Francis |
Volume: | 15 |
Number: | 3 |
Page Range: | 359-368 |
Date: | 4 March 2018 |
Official Publication: | https://doi.org/10.1080/15476286.2017.1384120 |
External Fulltext: | View full text on PubMed Central |
PubMed: | View item in PubMed |
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