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Related Concept Videos

Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
Experimental RNAi02:15

Experimental RNAi

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...
Transcriptional Regulation: Riboswitches01:23

Transcriptional Regulation: Riboswitches

Riboswitches are RNA elements that regulate gene expression by altering their secondary structures in response to specific effector molecules. These elements, located in the leader regions of certain mRNAs, act as transcriptional regulators by toggling between alternative conformations to control downstream gene expression. Riboswitch-mediated regulation is a precise mechanism for modulating biosynthetic pathways, as exemplified by the riboflavin biosynthesis pathway in Bacillus...

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Related Experiment Video

Updated: May 22, 2026

Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains
12:21

Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains

Published on: December 13, 2014

A new function of ROD1 in nonsense-mediated mRNA decay.

T F Brazão1, J Demmers, W van IJcken

  • 1Department of Cell Biology & Genetics, Erasmus MC, Rotterdam, The Netherlands. t.brazao@erasmusmc.nl

FEBS Letters
|May 12, 2012
PubMed
Summary
This summary is machine-generated.

ROD1, a paralog of polypyrimidine tract binding protein (PTBP), functions in nonsense-mediated mRNA decay (NMD). ROD1 interacts with UPF1 and regulates NMD targets, revealing a new role for PTBP paralogs in gene expression control.

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12:21

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Published on: December 13, 2014

Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing (RIPiT-Seq)
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08:53

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Area of Science:

  • Molecular Biology
  • Gene Regulation
  • RNA Processing

Background:

  • RNA-binding proteins regulate gene expression post-transcriptionally.
  • Polypyrimidine tract binding protein (PTBP) is a known splicing factor.
  • ROD1 is a PTBP paralog with four RNA recognition motif (RRM) domains.

Purpose of the Study:

  • To investigate the function of ROD1 in gene expression regulation.
  • To determine ROD1's role in nonsense-mediated mRNA decay (NMD).

Main Methods:

  • Protein-protein interaction studies (e.g., co-immunoprecipitation).
  • Reporter assays to assess mRNA destabilization.
  • RNA immunoprecipitation sequencing (RIP-seq) to identify target transcripts.

Main Results:

  • ROD1 interacts with the core NMD factor UPF1.
  • ROD1 and UPF1 co-regulate a large set of target genes.
  • ROD1 is essential for the destabilization of NMD substrates, similar to UPF1 and UPF2.
  • ROD1 and UPF1 bind to a substantial number of common transcripts.

Conclusions:

  • ROD1 plays a significant role in nonsense-mediated mRNA decay (NMD).
  • ROD1 acts in concert with UPF1 to regulate NMD pathway targets.
  • This study uncovers a novel function for PTBP paralogs in mRNA decay and gene regulation.