GOLGA2

From WikiMD's Wellness Encyclopedia

GOLGA2 (Golgin A2), also known as GM130, is a protein that in humans is encoded by the GOLGA2 gene. This protein is a member of the golgin family of proteins, which are localized to the Golgi apparatus. The Golgi apparatus is a critical organelle in the cell that is responsible for modifying, sorting, and packaging proteins and lipids for transport to different destinations within or outside the cell. GOLGA2 plays a significant role in the structure and function of the Golgi apparatus, particularly in the maintenance of its structure and in the process of vesicle trafficking.

Function[edit | edit source]

GOLGA2/GM130 is involved in several critical cellular processes, including the maintenance of the Golgi ribbon integrity, the regulation of the Golgi apparatus's structure during the cell cycle, and the mediation of vesicle docking and fusion. It acts as a tethering molecule, anchoring vesicles to the Golgi membrane, and is involved in the cis-Golgi network. Additionally, GOLGA2 is implicated in the Golgi reassembly stacking protein (GRASP) complex formation, which is essential for the reassembly of the Golgi stack during the M phase of the cell cycle.

Clinical Significance[edit | edit source]

Alterations in the expression or function of GOLGA2 have been associated with various diseases, including cancer and neurological disorders. Its role in vesicle trafficking and Golgi apparatus function suggests that GOLGA2 may influence the secretion of proteins that are critical for cell growth, signaling, and metabolism. Dysregulation of these processes can contribute to the development and progression of disease.

Molecular Biology[edit | edit source]

The GOLGA2 gene is located on chromosome 9q34.11 in humans. The protein encoded by this gene contains a conserved GRIP domain, which is essential for its localization to the Golgi apparatus. GOLGA2 interacts with several other proteins, including Rab1A, a small GTPase involved in vesicle trafficking, and GRASP65, another golgin involved in Golgi stacking.

Research Directions[edit | edit source]

Research on GOLGA2 continues to explore its precise functions within the cell, its interactions with other proteins, and its involvement in diseases. Understanding the molecular mechanisms underlying GOLGA2's role in Golgi apparatus function and vesicle trafficking may lead to the development of novel therapeutic strategies for diseases associated with Golgi dysfunction.


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Contributors: Prab R. Tumpati, MD