GOLGA4

From WikiMD's Food, Medicine & Wellness Encyclopedia

GOLGA4 (Golgin A4) is a protein that in humans is encoded by the GOLGA4 gene. This gene is a member of the golgin subfamily of the coiled-coil type of proteins, which are localized to the Golgi apparatus. Golgins play a significant role in the structure and function of the Golgi apparatus, involved in the tethering of transport vesicles and the maintenance of Golgi structural integrity. They are also implicated in various cellular processes including vesicle trafficking, apoptosis, and cell migration.

Function[edit | edit source]

The GOLGA4 protein is involved in maintaining the structural integrity of the Golgi apparatus and is essential for the proper functioning of the Golgi. It participates in the tethering of transport vesicles, which is crucial for the efficient transport of proteins and lipids within the cell. Additionally, GOLGA4 has been implicated in the process of mitosis, playing a role in the Golgi fragmentation and reassembly cycle that occurs during cell division.

Clinical Significance[edit | edit source]

Alterations in the expression or function of GOLGA4 have been associated with various human diseases, although the exact mechanisms remain under investigation. Studies have suggested a potential link between GOLGA4 and certain types of cancer, including prostate and ovarian cancer, where it may influence cancer cell proliferation and survival. Furthermore, due to its role in vesicle trafficking and cell migration, GOLGA4 is also being studied in the context of neurodegenerative diseases and its potential involvement in the pathological processes.

Genetic[edit | edit source]

The GOLGA4 gene is located on human chromosome 3q13.13. It consists of multiple exons and encodes the GOLGA4 protein, which is characterized by a coiled-coil domain, typical of golgins, facilitating its interaction with other proteins and its structural role in the Golgi apparatus.

Research Directions[edit | edit source]

Ongoing research is focused on elucidating the detailed mechanisms by which GOLGA4 contributes to Golgi apparatus function and cellular processes. Understanding the molecular pathways involving GOLGA4 may provide insights into the development of targeted therapies for diseases associated with Golgi dysfunction, including certain cancers and neurodegenerative disorders.

See Also[edit | edit source]

References[edit | edit source]



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Contributors: Prab R. Tumpati, MD