The multifaceted regulation of autophagy protein ATG16L1 and its implications in human diseases

ATG16L1 (autophagy related 16 like 1) is a core macroautophagy/autophagy protein essential for autophagosome formation. It also functions in non-canonical autophagy pathways such as LC3-associated phagocytosis (LAP) and in other processes including immunity, inflammation, and membrane trafficking. This review synthesizes recent advances and proposes that ATG16L1 functions as a central molecular integrator governed by a multi-layered regulatory code. This framework includes genetic polymorphisms, transcriptional control, and diverse post-transcriptional and post-translational mechanisms. We detail how these regulatory layers collectively fine-tune ATG16L1 function in response to cellular stress. Dysregulation of this network contributes broadly to human diseases including inflammatory bowel disease, cancer, and neurodegenerative disorders. Notably, the functional impact of specific regulatory events is highly context dependent, a principle exemplified by the Crohn disease-associated T300A polymorphism. Deciphering this regulatory landscape and its crosstalk with both autophagy-dependent and autophagy-independent functions positions ATG16L1 as a pivotal node in cellular homeostasis and as an emerging therapeutic target.

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Publication Details

Journal
Autophagy
Published
2026-05-10
DOI
https://doi.org/10.1080/15548627.2026.2672698
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
0.00

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article

The multifaceted regulation of autophagy protein ATG16L1 and its implications in human diseases

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Autophagy
Autophagy in Disease and Therapy
article

The multifaceted regulation of autophagy protein ATG16L1 and its implications in human diseases

Xiaozhu Zhao, Aimin Yang, Fujing Wei, Xiaoying Yu, Yuanhao Sun, Yue Wang, Xiaoxue Ke, Hongjuan Cui, Zhenzhen Liu, Ziling Feng, Yuanyuan Zhao
article en

Abstract

ATG16L1 (autophagy related 16 like 1) is a core macroautophagy/autophagy protein essential for autophagosome formation. It also functions in non-canonical autophagy pathways such as LC3-associated phagocytosis (LAP) and in other processes including immunity, inflammation, and membrane trafficking. This review synthesizes recent advances and proposes that ATG16L1 functions as a central molecular integrator governed by a multi-layered regulatory code. This framework includes genetic polymorphisms, transcriptional control, and diverse post-transcriptional and post-translational mechanisms. We detail how these regulatory layers collectively fine-tune ATG16L1 function in response to cellular stress. Dysregulation of this network contributes broadly to human diseases including inflammatory bowel disease, cancer, and neurodegenerative disorders. Notably, the functional impact of specific regulatory events is highly context dependent, a principle exemplified by the Crohn disease-associated T300A polymorphism. Deciphering this regulatory landscape and its crosstalk with both autophagy-dependent and autophagy-independent functions positions ATG16L1 as a pivotal node in cellular homeostasis and as an emerging therapeutic target.

Autophagy
Southwest University (CN), Chongqing University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Chongqing, Fundamental Research Funds for the Central Universities
Zero hunger
Openalex Percentile: Top 5%
Autophagy in Disease and Therapy
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