Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Jun;46(6):e2400038.
doi: 10.1002/bies.202400038. Epub 2024 May 9.

Omegasomes control formation, expansion, and closure of autophagosomes

Affiliations
Review

Omegasomes control formation, expansion, and closure of autophagosomes

Viola Nähse et al. Bioessays. 2024 Jun.

Abstract

Autophagy, an essential cellular process for maintaining cellular homeostasis and eliminating harmful cytoplasmic objects, involves the de novo formation of double-membraned autophagosomes that engulf and degrade cellular debris, protein aggregates, damaged organelles, and pathogens. Central to this process is the phagophore, which forms from donor membranes rich in lipids synthesized at various cellular sites, including the endoplasmic reticulum (ER), which has emerged as a primary source. The ER-associated omegasomes, characterized by their distinctive omega-shaped structure and accumulation of phosphatidylinositol 3-phosphate (PI3P), play a pivotal role in autophagosome formation. Omegasomes are thought to serve as platforms for phagophore assembly by recruiting essential proteins such as DFCP1/ZFYVE1 and facilitating lipid transfer to expand the phagophore. Despite the critical importance of phagophore biogenesis, many aspects remain poorly understood, particularly the complete range of proteins involved in omegasome dynamics, and the detailed mechanisms of lipid transfer and membrane contact site formation.

Keywords: DFCP1; FYVE domain; PI3P; omegasome; phagophore.

PubMed Disclaimer

Similar articles

References

REFERENCES

    1. Graef, M., Friedman, J. R., Graham, C., Babu, M., & Nunnari, J. (2013). ER exit sites are physical and functional core autophagosome biogenesis components. Molecular Biology of the Cell, 24(18), 2918–2931.
    1. Suzuki, K., Akioka, M., Kondo‐Kakuta, C., Yamamoto, H., & Ohsumi, Y. (2013). Fine mapping of autophagy‐related proteins during autophagosome formation in Saccharomyces cerevisiae. Journal of Cell Science, 126(Pt 11), 2534–2544.
    1. Ge, L., Melville, D., Zhang, M., & Schekman, R. (2013). The ER‐Golgi intermediate compartment is a key membrane source for the LC3 lipidation step of autophagosome biogenesis. Elife, 2, e00947.
    1. Puri, C., Renna, M., Bento, C. F., Moreau, K., & Rubinsztein, D. C. (2013). Diverse autophagosome membrane sources coalesce in recycling endosomes. Cell, 154(6), 1285–1299.
    1. Longatti, A., Lamb, C. A., Razi, M., Yoshimura, S. I., Barr, F. A., & Tooze, S. A. (2012). TBC1D14 regulates autophagosome formation via Rab11‐ and ULK1‐positive recycling endosomes. Journal of Cell Biology, 197(5), 659–675.

Substances

LinkOut - more resources