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Related Concept Videos

Transcription Attenuation in Prokaryotes02:42

Transcription Attenuation in Prokaryotes

Transcriptional attenuation occurs when RNA transcription is prematurely terminated due to the formation of a terminator mRNA hairpin structure.  Bacteria use these hairpins to regulate the transcription process and control the synthesis of several amino acids including histidine, lysine, threonine, and phenylalanine. Transcription attenuation takes place in the non-coding regions of mRNA.
There are several different mechanisms used to attenuate transcription. In ribosome mediated...
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart, a...
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
Conserved Binding Sites01:49

Conserved Binding Sites

Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
GPCR Desensitization01:12

GPCR Desensitization

G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...

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Related Experiment Video

Updated: May 27, 2026

Studying DNA Looping by Single-Molecule FRET
11:27

Studying DNA Looping by Single-Molecule FRET

Published on: June 28, 2014

Attenuation of loop-receptor interactions with pseudoknot formation.

Kirill A Afonin1, Yen-Ping Lin, Erin R Calkins

  • 1Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106-9510, USA.

Nucleic Acids Research
|November 15, 2011
PubMed
Summary

Natural RNA structures prefer A/U-rich sequences to avoid folding traps. This study shows G/C-rich RNA receptors can be trapped in pseudoknots, explaining evolutionary preferences and aiding synthetic biology designs.

Related Experiment Videos

Last Updated: May 27, 2026

Studying DNA Looping by Single-Molecule FRET
11:27

Studying DNA Looping by Single-Molecule FRET

Published on: June 28, 2014

Area of Science:

  • Molecular Biology
  • Structural Biology
  • RNA Biology

Background:

  • RNA tetraloops mediate long-range interactions in natural RNAs.
  • In vitro selected GNRA tetraloop/receptor interactions are often G/C-rich, unlike natural A/U-rich counterparts.
  • Evolutionary preference for A/U-rich sequences may prevent folding traps in larger RNA contexts.

Purpose of the Study:

  • Investigate the hypothesis that natural RNA evolution favors A/U-rich GNRA receptors to avoid folding traps.
  • Examine how G/C content in GNRA receptors affects their ability to form alternative intramolecular structures (pseudoknots).
  • Provide design principles for RNA-based attenuator devices.

Main Methods:

  • In vitro investigation of riboswitches with natural and artificial GNRA receptors.
  • Native gel-shift assays to determine interaction extents.
  • Co-transcriptional assembly to study RNA folding and interactions.

Main Results:

  • The extent of attenuation in riboswitches is correlated with the G/C content of the GNRA receptor.
  • G/C-rich GNRA receptors are more prone to being trapped in alternative intramolecular pseudoknots.
  • This trapping mechanism prevents intermolecular GNRA/receptor interactions.

Conclusions:

  • The G/C content of GNRA receptors influences their structural behavior and interaction potential.
  • Evolutionary selection may favor A/U-rich GNRA receptors to ensure proper RNA folding and function.
  • Findings offer insights into RNA structural evolution and guide the design of synthetic RNA devices.