Abstract
Genetic variations in the autophagic pathway influence genetic predispositions to Crohn disease. Autophagy, the major lysosomal pathway for degrading and recycling cytoplasmic material, constitutes an important homeostatic cellular process. Of interest, single-nucleotide polymorphisms in ATG16L1 (autophagy-related 16-like 1 [S. cerevisiae]), a key component in the autophagic response to invading pathogens, have been associated with an increased risk of developing Crohn disease. The most common and wellstudied genetic variant of ATG16L1 (rs2241880; leading to a T300A conversion) exhibits a strong association with risk for developing Crohn disease. The rs2241880 variant plays a crucial role in pathogen clearance, resulting in imbalanced cytokine production, and is linked to other biological processes, such as the endoplasmic reticulum stress/unfolded protein response. In this review, we focus on the importance of ATG16L1 and its genetic variant (T300A) within the elementary biological processes linked to Crohn disease.
| Original language | English |
|---|---|
| Journal | Autophagy |
| Volume | 11 |
| Issue number | 4 |
| Pages (from-to) | 585-94 |
| Number of pages | 10 |
| ISSN | 1554-8627 |
| DOIs | |
| Publication status | Published - 3 Apr 2015 |
Keywords
- Animals
- Autophagy
- Carrier Proteins
- Crohn Disease
- Endoplasmic Reticulum Stress
- Genetic Predisposition to Disease
- Humans
- Polymorphism, Single Nucleotide