Tandem repeat

Source: Wikipedia, the free encyclopedia.
Not to be confused with Tandemly arrayed genes.

In

primary structure, such as armadillo repeats. However, in proteins, perfect tandem repeats are unlikely in most in vivo proteins, and most known repeats are in proteins which have been designed.[2]

An example would be:

ATTCG ATTCG ATTCG

in which the sequence ATTCG is repeated three times.

Terminology

All tandem repeat arrays are classifiable as satellite DNA, a name originating from the fact that tandem DNA repeats, by nature of repeating the same nucleotide sequences repeatedly, have a unique ratio of the two possible nucleotide base pair combinations, conferring them a specific mass density that allows them to be separated from the rest of the genome with density-based laboratory techniques, thus appearing as "satellite bands." Albeit, a tandem repeat array could not show up as a satellite band if it had a nucleotide composition close to the average of the genome.[citation needed]

When exactly two nucleotides are repeated, it is called a dinucleotide repeat (for example: ACACACAC...). The

hereditary nonpolyposis colon cancer most commonly affects such regions.[3]

When three nucleotides are repeated, it is called a trinucleotide repeat (for example: CAGCAGCAGCAG...), and abnormalities in such regions can give rise to

trinucleotide repeat disorders
.

When between 10 and 60 nucleotides are repeated, it is called a

short tandem repeats
.

When much larger lengths of nucleotides are repeated, on the order of 1,000 nucleotides, it is called a macrosatellite.

When the repeat unit copy number is variable in the population being considered, it is called a variable number tandem repeat (VNTR). MeSH classifies variable number tandem repeats under minisatellites.[4]

Mechanism

Tandem repeats can occur through different mechanisms. For example, slipped strand mispairing (SSM), (also known as

replication slippage
), is a mutation process which occurs during DNA replication. It involves denaturation and displacement of the DNA strands, resulting in mispairing of the complementary bases. Slipped strand mispairing is one explanation for the origin and evolution of repetitive DNA sequences.

Other mechanisms include

unequal crossover and gene conversion
.

Uses

Tandem repeat describes a pattern that helps determine an individual's inherited traits.

Tandem repeats can be very useful in determining

microsatellites
within the chromosomal DNA. Parentage can be determined through the similarity in these regions.

Polymorphic tandem repeats (alias VNTRs) are also present in microorganisms and can be used to trace the origin of an outbreak. The corresponding assay in which a collection of VNTRs is typed to characterize a strain is most often called

monkeypox (mpox) virus genome during 2022 pandemic. [5]

In the field of

computer science, tandem repeats in strings (e.g., DNA sequences) can be efficiently detected using suffix trees or suffix arrays
.

Studies in 2004 linked the unusual genetic plasticity of dogs to mutations in tandem repeats.[6]

Nested tandem repeats are described as repeating unit lengths that are variable or unknown and frequently include an asymmetric hierarchy of smaller repeating units. These repeats are constructed from distinct groups of homologous-length monomers. An algorithm known as NTRprism was created by Oxford Nanopore Technologies researchers to enable for the annotation of repetitive structures in built satellite DNA arrays. The algorithm NTRprism is developed to find and display the satellite repeating periodicity.[7]

See also

References

  1. ^ Tandem+Repeat at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  2. PMID 20553501
    .
  3. PMID 10321739
    .
  4. ^ Variable+Number+of+Tandem+Repeats at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  5. PMID 36495863
    .
  6. S2CID 10680162
    .
  7. PMID 35357911
    .

External links
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