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Updated: Jun 2, 2025

Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions
Published on: June 28, 2018
Cohesin Complex Interacting with Promoters of MMP Genes for in Pterygium Occurrence
Shichao Han1, Wei Zhu1, Qianqian Guo1
1Department of Ophthalmology, Zibo Center Hospital, Zibo, China.
Purpose:
Pterygium is a common ocular surface disease characterized by a high recurrence rate and unknown etiology.
Methods:
In this study, we investigated the upregulation of matrix metalloproteinase genes, including MMP1, MMP2, MMP3, MMP7, MMP9, MMP11, MMP12, MMP13, MMP23B, and MMP28, in pterygium tissue using RNA sequencing, Western blotting, and immunohistochemistry.
Results:
Employing the MEME tool, we identified a conserved DNA motif within the promoter regions of these matrix metalloproteinase genes. Mass spectrometry analysis revealed an interaction between the cohesin complex and this motif. Disrupting the cohesin complex through RNA interference of RAD21 cohesin complex component or structural maintenance of chromosomes 3 in primary pterygial fibroblasts led to decreased matrix metalloproteinase gene expression and reduced recruitment of twist family bHLH transcription factor 1 and transcription factor 4 to matrix metalloproteinase gene promoters.
Conclusion:
Overall, our findings suggest a novel epigenetic mechanism regulating matrix metalloproteinase transcription in pterygium.
Insights
Researchers uncovered a new epigenetic mechanism in pterygium, a common eye condition. This involves the cohesin complex regulating matrix metalloproteinase gene expression, potentially explaining pterygium's recurrence.
Area of Science:
- Ophthalmology
- Molecular Biology
- Epigenetics
Background:
- Pterygium is a prevalent ocular surface disease with a high recurrence rate.
- The exact causes of pterygium remain largely unknown.
- Matrix metalloproteinases (MMPs) are implicated in tissue remodeling and inflammation.
Purpose of the Study:
- To investigate the role of matrix metalloproteinase (MMP) gene expression in pterygium.
- To identify regulatory mechanisms controlling MMP transcription in pterygium tissue.
Main Methods:
- RNA sequencing, Western blotting, and immunohistochemistry were used to analyze MMP gene expression.
- The MEME tool identified conserved DNA motifs in MMP gene promoters.
- Cohesin complex interactions and the effect of its disruption on MMP gene expression were studied using RNA interference and mass spectrometry.
Main Results:
- Upregulation of multiple matrix metalloproteinase (MMP) genes (MMP1, MMP2, MMP3, MMP7, MMP9, MMP11, MMP12, MMP13, MMP23B, MMP28) was observed in pterygium tissue.
- A conserved DNA motif interacting with the cohesin complex was identified in MMP gene promoters.
- Disrupting the cohesin complex reduced MMP gene expression and the recruitment of transcription factors (TWIST1, TCF4) to MMP promoters.
Conclusions:
- A novel epigenetic mechanism involving the cohesin complex regulates MMP gene transcription in pterygium.
- This finding provides new insights into the molecular pathogenesis of pterygium.
- Targeting this epigenetic pathway may offer therapeutic strategies for pterygium.
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