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Updated: Aug 7, 2026

Analysis of the c-KIT Ligand Promoter Using Chromatin Immunoprecipitation
Published on: June 27, 2017
A conserved quadruplex motif located in a transcription activation site of the human c-kit oncogene
Himesh Fernando1, Anthony P Reszka, Julian Huppert
1Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, United Kingdom.
Abstract:
The c-kit gene encodes a receptor tyrosine kinase, whose engagement by its ligand triggers signals leading to cell proliferation. c-kit activity is elevated in gastrointestinal stromal tumors (GISTs), and its therapeutic inhibition by small molecules such as imatinib is clinically validated. We identified a putative quadruplex forming 21-nucleotide sequence upstream of the c-kit transcription initiation site (c-kit21), on the G-rich strand, which occupies a site required for core promoter activity. Here, we show by nuclear magnetic resonance (NMR), circular dichroism (CD), and ultraviolet (UV) spectroscopic methods that c-kit21 forms quadruplexes under physiological conditions. Mutational analysis of c-kit21 has provided insights into its structural polymorphism. In particular, one mutated form appears to form a single quadruplex species that adopts a parallel conformation. The quadruplex-forming sequence shows a high level of sequence conservation across human, mouse, rat, and chimpanzee. The small variation in sequence between the quadruplex in human/chimpanzee as compared to the rat/mouse was examined more closely by biophysical methods. Despite a variation in the sequence and length of loop 2, the quadruplexes showed both comparable CD spectra, indicative of parallel quadruplexes, and also similar thermal-stability profiles, suggesting conservation of biophysical characteristics. Collectively, the evidence suggests that this quadruplex is a serious target for a detailed functional investigation at the cell-biology level.
Insights
Researchers found a G-rich DNA sequence (c-kit21) upstream of the c-kit gene forms stable quadruplex structures. This discovery suggests a potential new target for GIST therapies by modulating c-kit activity.
Area of Science:
- Molecular biology
- Genetics
- Biophysics
Background:
- The c-kit gene encodes a receptor tyrosine kinase crucial for cell proliferation.
- Elevated c-kit activity is linked to gastrointestinal stromal tumors (GISTs).
- Targeting c-kit with small molecules like imatinib is a validated therapeutic strategy.
Purpose of the Study:
- To investigate a putative quadruplex-forming sequence (c-kit21) upstream of the c-kit gene.
- To determine if c-kit21 forms quadruplex structures under physiological conditions.
- To analyze the structural characteristics and conservation of the c-kit21 quadruplex.
Main Methods:
- Nuclear magnetic resonance (NMR) spectroscopy
- Circular dichroism (CD) spectroscopy
- Ultraviolet (UV) spectroscopy
- Mutational analysis
- Biophysical characterization
Main Results:
- The c-kit21 sequence forms quadruplex structures under physiological conditions.
- Mutational analysis revealed structural polymorphism, with one mutant forming a parallel quadruplex.
- The quadruplex sequence is highly conserved across human, mouse, rat, and chimpanzee.
- Despite minor sequence variations, quadruplexes exhibited conserved biophysical characteristics.
Conclusions:
- The identified c-kit21 quadruplex is a stable structure with conserved biophysical properties.
- This quadruplex represents a potential novel therapeutic target for GISTs.
- Further cell-biology investigations are warranted to explore its functional significance.
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