Related Experiment Video
Updated: Apr 4, 2026

10:52
Sample Preparation for Mass Spectrometry-based Identification of RNA-binding Regions
Published on: September 28, 2017
8.7K
Bioinformatics Analysis to Identify RNA-Protein Interactions in Oogenesis
1Department of Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, CO, 80309, USA, rsingh@colorado.edu.
Methods in Molecular Biology (Clifton, N.J.)
|September 2, 2015
Summary
Researchers developed a bioinformatics method to find new messenger RNA (mRNA) targets for the Drosophila Sex-lethal (SXL) protein. This approach aids in understanding RNA-protein interactions in female germline development and other regulatory processes.
Area of Science:
- Molecular Biology
- Genetics
- Bioinformatics
Background:
- Hundreds of RNA-binding proteins (RBPs) play crucial roles in RNA processing and biogenesis.
- The specific biological functions of most RBPs remain largely unknown.
- Understanding RBP functions is key to deciphering gene regulation.
Purpose of the Study:
- To develop a bioinformatics approach for identifying novel mRNA targets of the Drosophila Sex-lethal (SXL) protein.
- To combine computational analysis with genetic and biochemical methods for target identification.
- To establish a framework for discovering new RNA-protein interactions.
Main Methods:
- Utilized a bioinformatics approach integrating computational analysis.
- Employed genetic investigation to validate predicted targets.
- Incorporated biochemical assays to confirm RNA-protein interactions.
- Focused on the Drosophila master sex-switch protein Sex-lethal (SXL).
Main Results:
- Successfully identified potential new mRNA targets for SXL.
- Demonstrated the feasibility of the combined computational and experimental approach.
- Provided insights into SXL's regulatory roles.
Conclusions:
- The developed bioinformatics approach is effective for identifying mRNA targets of RBPs.
- This method can be applied to study RNA-protein interactions during oogenesis in the female germline.
- The approach has broad applicability to numerous posttranscriptional regulatory events.
Related Concept Videos
Ribosome Profiling
4.3K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
4.3K
Protein Networks
4.7K
An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
4.7K
Protein-protein Interfaces
15.0K
Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
15.0K
RNA Interference
28.7K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
28.7K
Experimental RNAi
8.3K
RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
8.3K
piRNA - Piwi-interacting RNAs
7.9K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
7.9K

