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Related Concept Videos

Cryo-electron Microscopy01:28

Cryo-electron Microscopy

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Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
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RNA Structure01:19

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The basic structure of RNA consists of a string of ribonucleotides attached by phosphodiester bonds. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
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The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
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Nuclear Export of mRNA

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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...
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Nucleic Acids

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Nucleic acids are the most important macromolecules for the continuity of life. They carry the cell's genetic blueprint and carry instructions for its functioning.
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Protein Complex Assembly

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Related Experiment Video

Updated: Jun 13, 2025

Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events
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Naturally ornate RNA-only complexes revealed by cryo-EM.

Rachael C Kretsch1, Yuan Wu2, Svetlana A Shabalina3

  • 1Biophysics Program, Stanford University, Stanford, CA, USA.

Nature
|May 6, 2025
PubMed
Summary
This summary is machine-generated.

Researchers determined the 3D structures of three large bacterial RNAs, revealing complex RNA-only nanocages and dimeric complexes. These ornate RNA structures highlight their biological importance and self-assembly capabilities.

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Do's and Don'ts of Cryo-electron Microscopy: A Primer on Sample Preparation and High Quality Data Collection for Macromolecular 3D Reconstruction
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Nanomanipulation of Single RNA Molecules by Optical Tweezers
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Area of Science:

  • Structural Biology
  • RNA Biology
  • Bacterial Genetics

Background:

  • The three-dimensional structures of natural RNAs are largely unknown, potentially concealing significant biological functions.
  • Large, non-coding RNAs are increasingly recognized for their complex roles in cellular processes.

Purpose of the Study:

  • To elucidate the three-dimensional structures of three large, ornate bacterial RNAs using cryo-electron microscopy (cryo-EM).
  • To investigate the quaternary structures, assembly, and stability of these RNA complexes.
  • To explore the evolutionary conservation and biological significance of these RNA structures.

Main Methods:

  • Cryo-electron microscopy (cryo-EM) was employed to determine high-resolution 3D structures.
  • Bioinformatic analyses, including sequence covariation, were used to identify conserved interactions.
  • Biochemical assays were performed to assess complex stoichiometry and stability.

Main Results:

  • The structures of three large bacterial RNAs (GOLLD, ROOL, and OLE) were determined.
  • GOLLD and ROOL RNAs form RNA-only multimeric nanocages larger than the ribosome.
  • OLE RNA forms a dimeric complex with extensive coaxial stacking.
  • Multiple non-canonical interactions, including A-minor interactions and an A-A helix, stabilize these complexes.
  • RNA complex stoichiometries are maintained at lower concentrations than found in cells.

Conclusions:

  • Large, ornate RNA structures can form complex, protein-independent quaternary assemblies.
  • These RNA nanocages and complexes possess unique architectures stabilized by diverse intramolecular and intermolecular interactions.
  • Evolutionary conservation of intermolecular interactions underscores the biological relevance of these complex RNA structures.