Jump to content

Tandem repeat: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
Citation bot (talk | contribs)
Bots
5,441,542 edits
Add: authors 1-1. Removed proxy/dead URL that duplicated identifier. Removed parameters. Some additions/deletions were parameter name changes. | Use this bot. Report bugs. | Suggested by Abductive | Category:Articles to be expanded from September 2023 | #UCB_Category 288/741
→Terminology: explained the terminology of satellite DNA. Mentioned macrosatellites
Line 8: Line 8:


==Terminology==
==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 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.{{cn}}
⚫
{{Missing information|section|[[satellite DNA]]|date=September 2023}}When between 10 and 60 nucleotides are repeated, it is called a [[minisatellite]]. Those with fewer are known as [[Microsatellite (genetics)|microsatellite]]s or [[short tandem repeat]]s.


When exactly two nucleotides are repeated, it is called a ''dinucleotide repeat'' (for example: ACACACAC...). The [[microsatellite instability]] in [[hereditary nonpolyposis colon cancer]] most commonly affects such regions.<ref>{{cite journal |vauthors=Oki E, Oda S, Maehara Y, Sugimachi K |title=Mutated gene-specific phenotypes of dinucleotide repeat instability in human colorectal carcinoma cell lines deficient in DNA mismatch repair |journal=Oncogene |volume=18 |issue=12 |pages=2143–7 | date=March 1999 |pmid=10321739 |doi=10.1038/sj.onc.1202583|doi-access=free }}</ref>
When exactly two nucleotides are repeated, it is called a ''dinucleotide repeat'' (for example: ACACACAC...). The [[microsatellite instability]] in [[hereditary nonpolyposis colon cancer]] most commonly affects such regions.<ref>{{cite journal |vauthors=Oki E, Oda S, Maehara Y, Sugimachi K |title=Mutated gene-specific phenotypes of dinucleotide repeat instability in human colorectal carcinoma cell lines deficient in DNA mismatch repair |journal=Oncogene |volume=18 |issue=12 |pages=2143–7 | date=March 1999 |pmid=10321739 |doi=10.1038/sj.onc.1202583|doi-access=free }}</ref>


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 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 [[minisatellite]]. Those with fewer are known as [[Microsatellite (genetics)|microsatellite]]s or [[short tandem repeat]]s.

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). [[Medical Subject Headings|MeSH]] classifies variable number tandem repeats under minisatellites.<ref>{{MeshName|Variable+Number+of+Tandem+Repeats}}</ref>
When the repeat unit copy number is variable in the population being considered, it is called a [[variable number tandem repeat]] (VNTR). [[Medical Subject Headings|MeSH]] classifies variable number tandem repeats under minisatellites.<ref>{{MeshName|Variable+Number+of+Tandem+Repeats}}</ref>

Revision as of 02:19, 27 October 2023

Not to be confused with Tandemly arrayed genes.

Tandem repeats occur in DNA when a pattern of one or more nucleotides is repeated and the repetitions are directly adjacent to each other.[1] Several protein domains also form tandem repeats within their amino acid 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 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 microsatellite instability in 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 minisatellite. Those with fewer are known as microsatellites or 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 parentage. Short tandem repeats are used for certain genealogical DNA tests. DNA is examined from 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 MLVA (Multiple Loci VNTR Analysis).

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.[5]

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.[6]

See also

References

  1. ^ Tandem+Repeat at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  2. ^ Jorda J, Xue B, Uversky VN, Kajava AV (June 2010). "Protein tandem repeats - the more perfect, the less structured". The FEBS Journal. 277 (12): 2673–82. doi:10.1111/j.1742-4658.2010.07684.x. PMC 2928880. PMID 20553501.
  3. ^ Oki E, Oda S, Maehara Y, Sugimachi K (March 1999). "Mutated gene-specific phenotypes of dinucleotide repeat instability in human colorectal carcinoma cell lines deficient in DNA mismatch repair". Oncogene. 18 (12): 2143–7. doi:10.1038/sj.onc.1202583. PMID 10321739.
  4. ^ Variable+Number+of+Tandem+Repeats at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  5. ^ Pennisi E (December 2004). "Genetics. A ruff theory of evolution: gene stutters drive dog shape". Science. 306 (5705): 2172. doi:10.1126/science.306.5705.2172. PMID 15618495. S2CID 10680162.
  6. ^ Altemose, Nicolas; Logsdon, Glennis A.; Bzikadze, Andrey V.; Sidhwani, Pragya; Langley, Sasha A.; Caldas, Gina V.; Hoyt, Savannah J.; Uralsky, Lev; Ryabov, Fedor D.; Shew, Colin J.; Sauria, Michael E. G.; Borchers, Matthew; Gershman, Ariel; Mikheenko, Alla; Shepelev, Valery A. (April 2022). "Complete genomic and epigenetic maps of human centromeres". Science. 376 (6588): eabl4178. doi:10.1126/science.abl4178. ISSN 0036-8075. PMC 9233505. PMID 35357911.
Retrieved from "https://en.wikipedia.org/enwiki/w/index.php?title=Tandem_repeat&oldid=1182092027"