RBPome

RBPome catalogs RNA-binding proteins (RBPs) identified by RNA interactome capture (RIC) and enables analysis of their modulation by hypoxia and HIF-signaling in Caenorhabditis elegans, including vhl-1 loss-of-function mutants.


Key Features:

  • Global RBP catalog: Contains a detailed RBPome of more than 1,300 nematode RBPs, including 270 novel proteins identified by RNA interactome capture (RIC).
  • HIF-signaling modulation: Profiles changes in the RBPome under hypoxic conditions and in vhl-1 loss-of-function mutants to link HIF-signaling with RBP dynamics.
  • Data mining and visualization: Provides analytical support for mining and visualizing RIC-derived RBP datasets.
  • Differential RNA-binding analysis: Highlights differences in RNA-binding that are independent of protein abundance, indicating condition-specific RNA-binding changes such as those induced by hypoxia.

Scientific Applications:

  • Hypoxia response studies: Enables investigation of how hypoxia and HIF-signaling alter RBP composition and RNA interactions in C. elegans.
  • Longevity and organismal survival: Supports studies into RBP roles in longevity mechanisms and organismal adaptation to low-oxygen conditions.
  • Disease mechanism and therapeutic target discovery: Informs research on RBP involvement in disease progression and the identification of potential therapeutic targets relevant to hypoxia-related pathology.

Methodology:

RNA interactome capture (RIC) performed on wild-type Caenorhabditis elegans and vhl-1 loss-of-function mutants.

Topics

Details

Added:
1/14/2020
Last Updated:
1/15/2021

Operations

Publications

Esmaillie R, Ignarski M, Bohl K, Krüger T, Ahmad D, Seufert L, Schermer B, Benzing T, Müller R, Fabretti F. Activation of Hypoxia-Inducible Factor Signaling Modulates the RNA Protein Interactome in Caenorhabditis elegans. iScience. 2019;22:466-476. doi:10.1016/j.isci.2019.11.039. PMID:31835171. PMCID:PMC6926210.

PMID: 31835171
PMCID: PMC6926210
Funding: - National Institutes of Health: P40 OD010440 - Deutsche Forschungsgemeinschaft: BE2212, KFO329, MU3629/2\u20131, MU3629/3-1, SCHE1562/6