Homologous chromosome

Homologous Chromosomes are a pair of chromosomes, one from each parent, that have the same length, gene position, and centromere location. They are key players in the process of meiosis, where they pair up and exchange segments of DNA in a process known as crossing over.

Definition

Homologous chromosomes, also known as homologs, are two pieces of DNA within a diploid organism which carry the same genes, one from each parental source. They are similar but not identical, each carrying a different version of the same genes. These different versions of the same gene are called alleles.

Role in Meiosis

During meiosis, homologous chromosomes pair up in a process called synapsis. This pairing allows for the exchange of genetic material between homologous chromosomes, a process known as crossing over. This genetic recombination results in offspring that are genetically different from their parents, contributing to genetic diversity.

Role in Mitosis

In mitosis, homologous chromosomes do not pair up. Instead, each chromosome is replicated and the two copies, called sister chromatids, are distributed to the two daughter cells. This ensures that each daughter cell receives a complete set of chromosomes.

Disorders Involving Homologous Chromosomes

Errors in the separation of homologous chromosomes during meiosis can lead to disorders such as Down syndrome, where an individual has three copies of chromosome 21 instead of the usual two. Other disorders caused by such errors include Klinefelter syndrome, Turner syndrome, and Patau syndrome.

See Also

• Chromosome
• Gene
• Allele
• Meiosis
• Mitosis
• Crossing over
• Synapsis
• Sister chromatids
• Down syndrome
• Klinefelter syndrome
• Turner syndrome
• Patau syndrome

Homologous chromosome Resources
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