Procentriole

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Procentriole
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The procentriole is a small, cylindrical structure found in the centrosome of animal cells. It plays a crucial role in the formation of the centriole, which is essential for cell division and organization of the microtubule cytoskeleton. The procentriole is formed during the G1 phase of the cell cycle and serves as a template for the assembly of the centriole.

Structure[edit | edit source]

The procentriole consists of nine microtubule triplets arranged in a cylindrical shape. Each triplet is composed of three microtubules, with one microtubule from each triplet extending outwards to form the centriole. The procentriole is anchored to the mother centriole, which acts as a template for its assembly.

Function[edit | edit source]

The procentriole plays a crucial role in the duplication of the centrosome and the formation of the mitotic spindle during cell division. It serves as a platform for the assembly of the centriole, which is involved in the organization of the microtubule cytoskeleton and the formation of the spindle fibers.

During the G1 phase of the cell cycle, the procentriole begins to form adjacent to the mother centriole. It elongates and matures during the S phase, and by the G2 phase, it is fully formed and ready for duplication. The procentriole then serves as a template for the assembly of the daughter centriole, which is essential for the formation of the mitotic spindle.

Regulation[edit | edit source]

The formation and duplication of the procentriole are tightly regulated processes. Various proteins and signaling pathways are involved in the control of procentriole assembly and duplication. For example, the protein SAS-6 is essential for the initiation of procentriole formation, while the protein PLK4 is involved in the regulation of procentriole duplication.

Clinical Significance[edit | edit source]

Mutations or dysregulation of procentriole-related proteins can lead to various diseases and disorders. For example, defects in procentriole assembly and duplication have been associated with ciliopathies, which are a group of genetic disorders characterized by abnormalities in cilia structure and function. Cilia play important roles in cell signaling, sensory perception, and fluid movement, and their dysfunction can lead to a wide range of clinical manifestations.

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD