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Relationship: 2683
Title
dimerization, AHR/ARNT leads to Increase, slincR expression
Upstream event
Downstream event
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| Aryl hydrocarbon receptor activation leading to early life stage mortality via sox9 repression induced impeded craniofacial development | adjacent | Moderate | Moderate | Agnes Aggy (send email) | Under development: Not open for comment. Do not cite | EAGMST Under Review |
| Aryl hydrocarbon receptor activation leading to early life stage mortality via sox9 repression induced cardiovascular toxicity | adjacent | Moderate | Moderate | Allie Always (send email) | Under development: Not open for comment. Do not cite | EAGMST Under Review |
Taxonomic Applicability
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | High |
Life Stage Applicability
| Term | Evidence |
|---|---|
| Embryo | High |
| Development | High |
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Dimerization of Ahr/ARNT take place when the ligand-activated Ahr translocates to the nucleus from the cytoplasm.
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The Ahr/ARNT heterodimer can recognize aryl hydrocarbon response elements (AHREs), also known as xenobiotic response elements (XREs) or dioxin response elements (DREs), in the promoter region of downstream genes to regulate gene expression (Schmidt and Bradfield 1996). The target genes can either increase or decrease in their expression.
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slincR expression significantly increases when zebrafish are exposed to TCDD, and the slincR promoter includes the core AHRE (5’-T/GCGTG-3’) in multiple locations (Garcia et al., 2017), suggesting that slincR is a direct downstream target of the Ahr/ARNT heterodimer.
Evidence gathered for this KER is primarily from two main studies, (Garcia et al., 2017) and (Garcia et al., 2018), that discovered and described slincR in zebrafish.
| ID | Experimental Design | Species | Upstream Observation | Downstream Observation | Citation (first author, year) | Notes |
|---|
| Title | First Author | Biological Plausibility |
Dose Concordance |
Temporal Concordance |
Incidence Concordance |
|---|
Biological Plausibility
Dose Concordance Evidence
Temporal Concordance Evidence
Incidence Concordance Evidence
Uncertainties and Inconsistencies
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Certain PAHs, such as fluoranthene, phenanthrene, and 9-methylanthracene that significantly induce cyp1a greater than log2FC = 2, indicating that Ahr has been activated, do not induce slincR expression in zebrafish (Garcia et al., 2018).
- A TCDD dose-response experiment was conducted measuring gene expression changes of slincR and cyp1a (biomarker for Ahr activation) in 48 hpf zebrafish. While cyp1a expression was always higher than slincR, the expression of the two genes increased in parallel, with significant slincR expression being identified at and above 0.0625 ng/mL TCDD exposure concentration (Garcia et al., 2018).
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slincR expression increases in parallel with cyp1a when zebrafish are also exposed individually to several PAHs. Data come from a study that created a gene co-expression network and found that cyp1a and slincR expression were highly correlated with each other across multiple PAH treatments (Shankar et al., 2021).
Response-response Relationship
Time-scale
Known Feedforward/Feedback loops influencing this KER
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Ahr activation (and thus, the dimerization of Ahr/ARNT) resulting in significant slincR induction of expression has only been investigated in zebrafish and mice (Garcia et al., 2017; Garcia et al., 2018).