Codon
Codon is a sequence of three nucleotides that together form a unit of genetic code in a DNA or RNA molecule. The codon encodes a specific amino acid or a stop signal during protein synthesis. The genetic code is made up of 64 codons, each of which corresponds to a specific amino acid or a stop function in the synthesis process.
Structure and Function[edit | edit source]
A codon is composed of three consecutive nucleotides, and each nucleotide can be adenine (A), cytosine (C), guanine (G), or thymine (T) in DNA and uracil (U) in RNA. The sequence of nucleotides in a codon determines which amino acid will be added next to a growing protein chain or signals the termination of protein synthesis.
The process of translating codons into amino acids takes place in the ribosome, where mRNA is read and translated into protein with the help of tRNA (transfer RNA). Each tRNA molecule carries a specific amino acid and has an anticodon that pairs with the codon in mRNA.
Codon Usage[edit | edit source]
Codon usage varies among different organisms and can affect the efficiency and accuracy of protein synthesis. This variation is known as codon bias. Some codons are used more frequently in certain organisms, which can lead to variations in the speed and efficiency of protein synthesis.
Types of Codons[edit | edit source]
Codons can be classified into several types based on their function in protein synthesis:
- Start Codon: The start codon is the first codon of a mRNA transcript that is translated by a ribosome. The most common start codon is AUG, which codes for methionine in eukaryotes and a modified form of methionine (fMet) in prokaryotes.
- Sense Codons: These codons code for one of the twenty standard amino acids used to build proteins.
- Stop Codons: Also known as nonsense codons, these signal the end of protein synthesis. The three stop codons are UAA, UAG, and UGA.
Genetic Code Table[edit | edit source]
The genetic code is typically represented by a table that maps codons to their corresponding amino acids. This table is crucial for understanding how proteins are encoded by genetic material.
Mutations and Codons[edit | edit source]
Changes in the nucleotide sequence of a codon can lead to mutations, which may affect protein function. These changes can be:
- Silent Mutations: These mutations do not change the amino acid sequence of the protein due to the redundancy of the genetic code.
- Missense Mutations: These result in a different amino acid and can affect the function of the protein.
- Nonsense Mutations: These change a sense codon into a stop codon, leading to premature termination of protein synthesis.
Clinical Significance[edit | edit source]
Understanding codons and their implications in genetic coding is essential for fields like genetic engineering, biotechnology, and medicine. Mutations in codons can lead to various genetic disorders and are a key area of study in the treatment of diseases.
Navigation: Wellness - Encyclopedia - Health topics - Disease Index - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Contributors: Prab R. Tumpati, MD