Monocentric chromosome

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Monocentric chromosomes are a type of chromosome characterized by having a single centromere. The centromere is a region of the chromosome that is essential for the correct distribution of chromosomes to daughter cells during cell division. In monocentric chromosomes, this centromere serves as the point of attachment for spindle fibers during mitosis and meiosis, facilitating the segregation of chromosomes into daughter cells.

Structure[edit | edit source]

Monocentric chromosomes consist of two arms, known as the p (short) arm and the q (long) arm, which are joined by a single centromere. The location of the centromere gives the chromosome its characteristic shape and can vary among different chromosomes. Depending on the position of the centromere, chromosomes can be classified as metacentric, submetacentric, acrocentric, or telocentric. However, in the case of monocentric chromosomes, the focus is on the presence of a single, centrally located centromere.

Function[edit | edit source]

The primary function of the centromere in monocentric chromosomes is to ensure the accurate segregation of chromosomes during cell division. The centromere acts as the attachment site for spindle fibers, which are structures that pull the chromosomes apart to opposite poles of the cell. This process is crucial for maintaining the integrity of the genetic material passed on to daughter cells.

Comparison with Holocentric Chromosomes[edit | edit source]

Unlike monocentric chromosomes, holocentric chromosomes do not have a single, localized centromere. Instead, holocentric chromosomes possess multiple centromere-like regions along their length, allowing for attachment of spindle fibers at multiple points. This difference in centromere structure has implications for the mechanisms of chromosome segregation during cell division.

Clinical Significance[edit | edit source]

Abnormalities in the structure or function of the centromere can lead to chromosomal instability, which is associated with various genetic disorders and diseases. For example, mutations affecting the centromere can result in aneuploidy, a condition characterized by an abnormal number of chromosomes, which is a common feature in many cancers.

Research[edit | edit source]

Research into the structure and function of monocentric chromosomes, as well as the proteins that interact with the centromere, continues to provide insights into the complex processes of cell division and genetic inheritance. Understanding these mechanisms is crucial for developing new therapeutic strategies for diseases associated with chromosomal abnormalities.


The image above contains clickable links
A chromosome and its packaged long strand of DNA unraveled. The DNA's base pairs encode genes, which provide functions. A human DNA can have up to 500 million base pairs with thousands of genes.


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Contributors: Prab R. Tumpati, MD