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Updated: Aug 5, 2026

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3D Imaging of PDL Collagen Fibers during Orthodontic Tooth Movement in Mandibular Murine Model
Published on: April 15, 2021
Association Between Single-Nucleotide Polymorphisms and DRAM1 Gene Expression in Periodontal Ligament Fibroblasts
Rebecca Linke1, Erika Calvano Küchler1, Peter Proff2
1Department of Orthodontics, Medical Faculty, University of Bonn, 53111 Bonn, Germany.
Biomedicines
|July 28, 2026
Summary
Investigating DNA damage-regulated autophagy modulator 1 (DRAM1) single-nucleotide polymorphisms (SNPs) in human periodontal ligament fibroblasts revealed no significant impact on gene expression under orthodontic compression. The studied DRAM1 SNPs did not appear to regulate gene expression during tooth movement.
Area of Science:
- Genetics
- Cell Biology
- Orthodontics
Background:
- Autophagy is crucial for orthodontic tooth movement.
- DNA damage-regulated autophagy modulator 1 (DRAM1) regulates autophagic cargo degradation.
- DRAM1 expression is differentially regulated in human periodontal ligament (hPDL) fibroblasts under compressive force.
Purpose of the Study:
- To investigate the impact of DRAM1 single-nucleotide polymorphisms (SNPs) on DRAM1 gene expression in hPDL fibroblasts under compressive force.
- To determine if specific DRAM1 SNPs influence gene expression during simulated orthodontic tooth movement.
Main Methods:
- hPDL fibroblasts from 59 patients were subjected to a compressive strain of 2 g/cm³.
- Relative DRAM1 gene expression was measured under loaded and control conditions.
- Genotyping analysis of six DRAM1 SNPs (rs756534, rs2138257, rs2176092, rs4622329, rs10860812, rs4764657) was performed using real-time PCR.
- Linear regression was used to evaluate SNP-SNP interactions.
Main Results:
- No statistically significant differences in relative DRAM1 gene expression were observed among the genotypes of the studied SNPs (p > 0.05).
- SNP-SNP interaction analysis did not reveal any statistically significant associations.
- The tested intronic SNPs within the DRAM1 gene did not show a regulatory role in gene expression under orthodontic compression.
Conclusions:
- The expression of DRAM1 in hPDL fibroblasts under orthodontic compression is not significantly regulated by the investigated intronic SNPs.
- These findings suggest that other regulatory mechanisms may be involved in DRAM1 modulation during orthodontic tooth movement.
- Further research is needed to explore other genetic variants or regulatory factors influencing DRAM1 in this context.
