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Related Concept Videos

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
Translation01:31

Translation

Lesson: Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Translation01:31

Translation

Lesson: Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Genome Copying Errors02:46

Genome Copying Errors

DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
Alternative RNA Splicing02:18

Alternative RNA Splicing

Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...

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Related Experiment Video

Updated: Jun 10, 2026

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
05:37

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes

Published on: April 4, 2025

G-quadruplex nucleic acids and human disease.

Yuliang Wu1, Robert M Brosh

  • 1Laboratory of Molecular Gerontology, National Institute on Aging, Baltimore, MD, USA.

The FEBS Journal
|July 31, 2010
PubMed
Summary
This summary is machine-generated.

G-quadruplex (G4) DNA structures, distinct from B-DNA, are found in the human genome. These structures impact DNA replication, transcription, and genomic stability, linking G4 DNA to human genetic diseases and cancer.

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Area of Science:

  • Genetics
  • Molecular Biology
  • Biochemistry

Background:

  • Alternate DNA structures, like G-quadruplex (G4) DNA, exist in the human genome.
  • G4 structures are formed by stacked guanine quartets via Hoogsteen hydrogen bonding.
  • These structures can influence DNA replication, transcription, and genomic stability.

Purpose of the Study:

  • To review the connections between G-quadruplex nucleic acids and human genetic diseases.
  • To explore the role of G4 structures in cancer development.
  • To summarize recent literature on G4 DNA in disease.

Main Methods:

  • Literature review of recent studies.
  • Analysis of G-quadruplex formation in G-rich genomic regions.
  • Examination of G4 DNA helicase roles in disease.

Main Results:

  • G-quadruplex structures affect key cellular processes like replication and transcription.
  • Telomere maintenance is linked to G4 structures at telomere ends.
  • Defects in G4 DNA helicases correlate with telomere instability and replication issues.

Conclusions:

  • G-quadruplex DNA plays a significant role in human genetic diseases, including cancer.
  • Telomere stability and genomic integrity are influenced by G4 structures.
  • Further research into G4 DNA is crucial for understanding and treating associated diseases.