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Related Concept Videos

Translational Regulation01:29

Translational Regulation

Translational regulation in prokaryotes ensures efficient protein synthesis by controlling ribosome access to mRNA. This regulation is mediated by secondary RNA structures, including translational riboswitches, RNA thermometers, and small RNAs (sRNAs), which respond to intracellular and environmental signals to modulate gene expression.Translational RiboswitchesRiboswitches in the leader region of mRNAs can regulate translation by altering the accessibility of the Shine-Dalgarno (SD) sequence,...
RNA Interference01:23

RNA Interference

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...
RNA Interference01:23

RNA Interference

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.
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Bacterial Protein Maturation01:26

Bacterial Protein Maturation

Bacterial protein maturation is a tightly regulated process that ensures newly synthesized polypeptides achieve correct functional conformations. This maturation involves a series of modifications, folding events, and quality control steps, often assisted by specialized chaperone proteins.N-Terminal ModificationsThe maturation of bacterial polypeptides begins cotranslationally as the polypeptide exits the ribosome. The first amino acid, N-formylmethionine (fMet), is typically modified at the...
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...
siRNA - Small Interfering RNAs02:30

siRNA - Small Interfering RNAs

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Related Experiment Video

Updated: Jun 16, 2026

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using &#967;CRAC
09:15

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC

Published on: May 9, 2020

CISP, an Intrinsically Disordered Cold-Inducible Barley Protein, Functions as a Small RNA Chaperone.

Yutaro Okumura1, Md Maksudul Haque1, Shin-Ichiro Kidou1,2

  • 1Graduate School of Science Nagoya City University Nagoya Japan.

Plant Direct
|June 15, 2026
PubMed
Summary
This summary is machine-generated.

A novel barley protein, CISP, enhances growth in low temperatures by acting as an RNA chaperone. This discovery offers new strategies for improving crop cold tolerance through molecular breeding.

Keywords:
CISPRNA chaperonebarleycold toleranceintrinsically disordered protein (IDPs)

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Using Caenorhabditis elegans to Screen for Tissue-Specific Chaperone Interactions
06:55

Using Caenorhabditis elegans to Screen for Tissue-Specific Chaperone Interactions

Published on: June 7, 2020

Related Experiment Videos

Last Updated: Jun 16, 2026

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using &#967;CRAC
09:15

Monitoring Protein-RNA Interaction Dynamics In Vivo at High Temporal Resolution Using χCRAC

Published on: May 9, 2020

Using Caenorhabditis elegans to Screen for Tissue-Specific Chaperone Interactions
06:55

Using Caenorhabditis elegans to Screen for Tissue-Specific Chaperone Interactions

Published on: June 7, 2020

Area of Science:

  • Plant Biology
  • Molecular Biology
  • Biochemistry

Background:

  • Low temperatures pose significant stress, limiting plant growth and crop yields.
  • Understanding molecular mechanisms of cold tolerance is crucial for agricultural improvement via molecular breeding.

Purpose of the Study:

  • To investigate the function of CISP, a barley protein induced by cold stress.
  • To determine CISP's role in promoting growth under low temperatures and its molecular activity.

Main Methods:

  • Heterologous expression of CISP in *Escherichia coli* and *Arabidopsis thaliana* to assess growth promotion.
  • RNA chaperone assays using RNA beacons to evaluate CISP's effect on RNA secondary structures.

Main Results:

  • CISP expression enhanced bacterial and plant seedling growth at low temperatures.
  • CISP demonstrated RNA chaperone activity by reducing and destabilizing RNA secondary structures.
  • CISP, a basic protein with an intrinsically disordered N-terminal region, lacks canonical RNA-binding domains.

Conclusions:

  • CISP promotes growth in heterologous organisms under cold stress, suggesting a conserved function.
  • CISP exhibits RNA chaperone activity, potentially representing a novel class of RNA chaperones.
  • CISP offers new insights into barley cold tolerance mechanisms and potential applications in crop improvement.