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Related Concept Videos

Ribosome Profiling02:24

Ribosome Profiling

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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.
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The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
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The central dogma explains the flow of genetic information from DNA nucleotides to the amino acid sequence of proteins.
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Prokaryotic genomes exhibit a streamlined organization of coding and non-coding regions essential for gene expression and protein synthesis. While coding regions contain the genetic instructions for proteins or functional RNAs, non-coding regions regulate the precise transcription and translation of these genes.Coding Regions: Proteins and RNAsThe primary coding regions, known as structural genes, include sequences transcribed into messenger RNA (mRNA) and ultimately translated into...
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Related Experiment Video

Updated: Jul 12, 2025

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
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Protein-coding potential of non-canonical open reading frames in human transcriptome.

Hitesh Kore1, Keshava K Datta2, Shivashankar H Nagaraj3

  • 1Centre for Genomics and Personalised Health, Queensland University of Technology, Brisbane, Queensland, 4059, Australia; Cancer Precision Medicine Group, QIMR Berghofer Medical Research Institute, 300 Herston Road, Herston, Queensland, 4006, Australia; Faculty of Health, Queensland University of Technology, Brisbane, Queensland, 4059, Australia.

Biochemical and Biophysical Research Communications
|October 28, 2023
PubMed
Summary

Recent studies reveal numerous small open reading frame encoded proteins (SEPs) from human noncoding DNA. While many are poorly conserved, some SEPs are crucial for biological functions and diseases.

Keywords:
Non-coding RNAsNovel proteinsProtein-coding potentialSEPs

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Area of Science:

  • Genomics
  • Proteomics
  • Molecular Biology

Background:

  • Proteogenomics and ribosome profiling reveal novel proteins from human noncoding genome regions.
  • These small open reading frame encoded proteins (SEPs) originate from untranslated regions (UTRs) of mRNAs and long non-coding RNAs (lncRNAs).
  • SEPs are typically short (<150 amino acids) and exhibit limited evolutionary conservation.

Conclusions:

  • The full extent and functional importance of novel protein-coding regions in the human genome remain incompletely understood.
  • Continued research is vital for accurate annotation and understanding the roles of SEPs.
  • SEPs represent a significant, yet underexplored, component of the human proteome.