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Repeated sequence (DNA)

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Repeated sequences (also known as repetitive elements, repeating units or repeats) are short or long patterns that occur in multiple copies throughout the genome. In many organisms, a significant fraction of the genomic DNA is repetitive, with over two-thirds of the sequence consisting of repetitive elements in humans.[1] Some of these repeated sequences are necessary for maintaining important genome structures such as telomeres or centromeres.[2]

Repeated sequences are categorized into different classes depending on features such as structure, length, location, origin, and mode of multiplication. The disposition of repetitive elements throughout the genome can consist either in directly adjacent arrays called tandem repeats or in repeats dispersed throughout the genome called interspersed repeats.[3] Tandem repeats and interspersed repeats are further categorized into subclasses based on the length of the repeated sequence and/or the mode of multiplication.

While some repeated DNA sequences are important for cellular functioning and genome maintenance, other repetitive sequences can be harmful. Many repetitive DNA sequences have been linked to human diseases such as Huntington's disease and Friedreich's ataxia. Some repetitive elements are neutral and occur when there is an absence of selection for specific sequences depending on how transposition or crossing over occurs.[2] However, an abundance of neutral repeats can still influence genome evolution as they accumulate over time. Overall, repeated sequences are an important area of focus because they can provide insight into human diseases and genome evolution.[2]

History

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In the 1950s, Barbara McClintock first observed DNA transposition and illustrated the functions of the centromere and telomere at the Cold Spring Harbor Symposium.[4] McClintock's work set the stage for the discovery of repeated sequences because transposition, centromere structure, and telomere structure are all possible through repetitive elements, yet this was not fully understood at the time. The term "repeated sequence" was first used by Roy John Britten and D. E. Kohne in 1968; they found out that more than half of the eukaryotic genomes were repetitive DNA through their experiments on reassociation of DNA.[5] Although the repetitive DNA sequences were conserved and ubiquitous, their biological role was yet unknown. In the 1990s, more research was conducted to elucidate the evolutionary dynamics of minisatellite and microsatellite repeats because of their importance in DNA-based forensics and molecular ecology. DNA-dispersed repeats were increasingly recognized as a potential source of genetic variation and regulation. Discoveries of deleterious repetitive DNA-related diseases stimulated further interest in this area of study.[6] In the 2000s, the data from full eukaryotic genome sequencing enabled the identification of different promoters, enhancers, and regulatory RNAs which are all coded by repetitive regions. Today, the structural and regulatory roles of repetitive DNA sequences remain an active area of research.

Types and functions

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Many repeat sequences are likely to be non-functional, decaying remnants of Transposable elements, these have been labelled "junk" or "selfish" DNA.[7][8][9] Nevertheless, occasionally some repeats may be exapted for other functions.[10]

Tandem repeats

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Tandem repeats are repeated sequences which are directly adjacent to each other in the genome.[11] Tandem repeats may vary in the number of nucleotides comprising the repeated sequence, as well as the number of times the sequence repeats. When the repeating sequence is only 2–10 nucleotides long, the repeat is referred to as a short tandem repeat (STR) or microsatellite.[12] When the repeating sequence is 10–60 nucleotides long, the repeat is referred to as a minisatellite.[13] For minisatellites and microsatellites, the number of times the sequence repeats at a single locus can range from twice to hundreds of times.

Tandem repeats have a wide variety of biological functions in the genome. For example, minisatellites are often hotspots of meiotic homologous recombination in eukaryotic organisms.[14] Recombination is when two homologous chromosomes align, break, and rejoin to swap pieces. Recombination is important as a source of genetic diversity, as a mechanism for repairing damaged DNA, and a necessary step in the appropriate segregation of chromosomes in meiosis.[14] The presence of repeated sequence DNA makes it easier for areas of homology to align, thereby controlling when and where recombination occurs.

In addition to playing an important role in recombination, tandem repeats also play important structural roles in the genome. For example, telomeres are composed mainly of tandem TTAGGG repeats.[15] These repeats fold into highly organized G quadruplex structures which protect the ends of chromosomal DNA from degradation.[16] Repetitive elements are enriched in the middle of chromosomes as well. Centromeres are the highly compact regions of chromosomes which join sister chromatids together and also allow the mitotic spindle to attach and separate sister chromatids during cell division.[17] Centromeres are composed of a 177 base pair tandem repeat named the α-satellite repeat.[16] Pericentromeric heterochromatin, the DNA which surrounds the centromere and is important for structural maintenance, is composed of a mixture of different satellite subfamilies including the α-, β- and γ-satellites as well as HSATII, HSATIII, and sn5 repeats.[18]

Tandem and interspersed repeat

Some repetitive sequences, such as those with structural roles discussed above, play roles necessary for proper biological functioning. Other tandem repeats have deleterious roles which drive diseases. Many other tandem repeats, however, have unknown or poorly understood functions.[19]

Interspersed repeats

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Interspersed repeats are identical or similar DNA sequences which are found in different locations throughout the genome.[20] Interspersed repeats are distinguished from tandem repeats in that the repeated sequences are not directly adjacent to each other but instead may be scattered among different chromosomes or far apart on the same chromosome. Most interspersed repeats are transposable elements (TEs), mobile sequences which can be "cut and pasted" or "copied and pasted" into different places in the genome.[21] TEs were originally called "jumping genes" for their ability to move, yet this term is somewhat misleading as not all TEs are discrete genes.[22]

Transposable elements that are transcribed into RNA, reverse-transcribed into DNA, then reintegrated into the genome are called retrotransposons.[21] Just as tandem repeats are further subcategorized based on the length of the repeating sequence, there are many different types of retrotransposons. Long interspersed nuclear elements (LINEs) are typically 3–7 kilobases in length.[23] Short interspersed nuclear elements (SINEs) are typically 100-300 base pairs and no longer than 600 base pairs.[23] Long-terminal repeat retrotransposons (LTRs) are a third major class of retrotransposons and are characterized by highly repetitive sequences as the ends of the repeat.[21] When a transposable element does not proceed through RNA as an intermediate, it is called a DNA transposon.[21] Other classification systems refer to retrotransposons as "Class I" and DNA transposons as "Class II" transposable elements.[22]

Transposable elements are estimated to constitute 45% of the human genome.[24] Since uncontrolled propagation of TEs could wreak havoc on the genome, many regulatory mechanisms have evolved to silence their spread, including DNA methylation, histone modifications, non-coding RNAs (ncRNAs) including small interfering RNA (siRNA), chromatin remodelers, histone variants, and other epigenetic factors.[22] However, TEs play a wide variety of important biological functions. When TEs are introduced into a new host, such as from a virus, they increase genetic diversity.[22] In some cases, host organisms find new functions for the proteins which arise from expressing TEs in an evolutionary process called TE exaptation.[22] Recent research also suggests that TEs serve to maintain higher-order chromatin structure and 3D genome organization.[25] Furthermore, TEs contribute to regulating the expression of other genes by serving as distal enhancers and transcription factor binding sites.[26]

The prevalence of interspersed elements in the genome has garnered attention for more research on their origins and functions. Some specific interspersed elements have been characterized, such as the Alu repeat and LINE1.

Intrachromosomal recombination

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Homologous recombination between chromosomal repeated sequences in somatic cells of Nicotiana tabacum was found to be increased by exposure to mitomycin C, a bifunctional alkylating agent that crosslinks DNA strands.[27] This increase in recombination was attributed to increased intrachromosomal recombinational repair.[27] By this process, mitomycin C damaged DNA in one sequence is repaired using intact information from the other repeated sequence.

Direct and inverted repeats

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While tandem and interspersed repeats are distinguished based on their location in the genome, direct and inverted repeats are distinguished based on the ordering of the nucleotide bases. Direct repeats occur when a nucleotide sequence is repeated with the same directionality. Inverted repeats occur when a nucleotide sequence is repeated in the inverse direction. For example, a direct repeat of "CATCAT" would be another repetition of "CATCAT". In contrast, the inverted repeated would be "ATGATG". When there are no nucleotides separating the inverted repeat, such as "CATCATATGATG", the sequence is called a palindromic repeat. Inverted repeats can play structural roles in DNA and RNA by forming stem loops and cruciforms.[28]

Repeated sequences in human disease

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For humans, some repeated DNA sequences are associated with diseases. Specifically, tandem repeat sequences, underlie several human disease conditions, particularly trinucleotide repeat diseases such as Huntington's disease, fragile X syndrome, several spinocerebellar ataxias, myotonic dystrophy and Friedreich's ataxia.[29] Trinucleotide repeat expansions in the germline over successive generations can lead to increasingly severe manifestations of the disease. These trinucleotide repeat expansions may occur through strand slippage during DNA replication or during DNA repair synthesis.[29] It has been noted that genes containing pathogenic CAG repeats often encode proteins that themselves have a role in the DNA damage response and that repeat expansions may impair specific DNA repair pathways.[30] Faulty repair of DNA damages in repeat sequences may cause further expansion of these sequences, thus setting up a vicious cycle of pathology.[30]

Huntington's disease

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Image of the repeated DNA sequence in Huntington's disease.

Huntington's disease is a neurodegenerative disorder which is due to the expansion of repeated trinucleotide sequence CAG in exon 1 of the huntingtin gene (HTT). This gene is responsible for encoding the protein huntingtin which plays a role in preventing apoptosis,[31] otherwise known as cell death, and repair of oxidative DNA damage.[32] In Huntington's disease the expansion of the trinucleotide sequence CAG encodes for a mutant huntingtin protein with an expanded polyglutamine domain.[33] This domain causes the protein to form aggregates in nerve cells preventing normal cellular function and resulting in neurodegeneration.

Fragile X repeated CCG DNA sequence in comparison to a normal X chromosome.

Fragile X syndrome

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Fragile X syndrome is caused by the expansion of the DNA sequence CCG in the FMR1 gene on the X chromosome.[34] This gene produces the RNA-binding protein FMRP. In the case of Fragile X syndrome the repeated sequence makes the gene unstable and therefore silences the gene FMR1.[35] Because the gene resides on the X chromosome, females who have two X chromosomes are less effected than males who only have on X chromosome and one Y chromosome because the second X chromosome can compensate for the silencing of the gene on the other X chromosome.

Spinocerebellar ataxias

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The disease spinocerebellar ataxias has CAG trinucleotide repeat sequences that underlie several types of spinocerebellar ataxias (SCAs-SCA1; SCA2; SCA3; SCA6; SCA7; SCA12; SCA17).[36] Similar to Huntington's disease, the polyglutamine tail created due to this trinucleotide expansion causes aggregation of proteins, preventing normal cellular function and causing neurodegeneration.[37]

Friedreich's Ataxia

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Friedreich's ataxia is a type of ataxia that has an expanded repeat sequence GAA in the frataxin gene.[38] The frataxin gene is responsible for producing the frataxin protein, which is a mitochondrial protein involved in energy production and cellular respiration.[39] The expanded GAA sequence results in the silencing of the first intron resulting in loss of function in the frataxin protein. The loss of a functional FXN gene leads to issues with mitochondrial functioning as a whole and can present phenotypically in patients as difficulty walking.

Myotonic dystrophy

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Myotonic dystrophy is a disorder that presents as muscle weakness and consists of two main types: DM1 and DM2.[40] Both types of myotonic dystrophy are due to expanded DNA sequences. In DM1 the DNA sequence that is expanded is CTG while in DM2 it is CCTG. These two sequences are found on different genes with the expanded sequence in DM2 being found on the ZNF9 gene and the expanded sequence in DM1 found on the DMPK gene. The two genes don't encode for proteins unlike other disorders like Huntington's disease or Fragile X syndrome. It has been shown, however, that there is a link between RNA toxicity and the repeat sequences in DM1 and DM2.

Amyotrophic lateral sclerosis and Frontotemporal dementia

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Not all diseases caused by repeated DNA sequences are trinucleotide repeat diseases. The diseases amyotrophic lateral sclerosis and frontotemporal dementia are caused by hexanucleotide GGGGCC repeat sequences in the C9orf72 gene, causing RNA toxicity that leads to neurodegeneration.[41][36]

Biotechnology

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Repetitive DNA is hard to sequence using next-generation sequencing techniques because sequence assembly from short reads simply cannot determine the length of a repetitive part. This issue is particularly serious for microsatellites, which are made of tiny 1-6bp repeat units.[42] Although they are difficult to sequence, these short repeats have great value in DNA fingerprinting and evolutionary studies. Many researchers have historically left out repetitive sequences when analyzing and publishing whole genome data due to technical limitations.[43]

Bustos. et al. proposed one method of sequencing long stretches of repetitive DNA.[42] The method combines the use of a linear vector for stabilization and exonuclease III for deletion of continuing simple sequence repeats (SSRs) rich regions. First, SSR-rich fragments are cloned into a linear vector that can stably incorporate tandem repeats up to 30kb. Expression of repeats is prohibited by the transcriptional terminators in the vector. The second step involves the use of exonuclease III. The enzyme can delete nucleotide at the 3' end which results in the production of a unidirectional deletion of SSR fragments. Finally, this product which has deleted fragments is multiplied and analyzed with colony PCR. The sequence is then built by an ordered sequencing of a set of clones containing different deletions.

See also

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References

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  1. ^ de Koning AP, Gu W, Castoe TA, Batzer MA, Pollock DD (December 2011). "Repetitive elements may comprise over two-thirds of the human genome". PLOS Genetics. 7 (12): e1002384. doi:10.1371/journal.pgen.1002384. PMC 3228813. PMID 22144907.
  2. ^ a b c Lower SE, Dion-Côté AM, Clark AG, Barbash DA (November 2019). "Special Issue: Repetitive DNA Sequences". Genes. 10 (11): 896. doi:10.3390/genes10110896. PMC 6895920. PMID 31698818.
  3. ^ "Repeated Sequence (DNA) — an overview". ScienceDirect Topics. ScienceDirect. Retrieved 2022-10-04.
  4. ^ McClintock B (1951-01-01). "Chromosome organization and genic expression". Cold Spring Harbor Symposia on Quantitative Biology. 16: 13–47. doi:10.1101/sqb.1951.016.01.004. PMID 14942727.
  5. ^ Britten RJ, Kohne DE (August 1968). "Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms". Science. 161 (3841): 529–540. doi:10.1126/science.161.3841.529. PMID 4874239.
  6. ^ Shapiro JA, von Sternberg R (May 2005). "Why repetitive DNA is essential to genome function". Biological Reviews of the Cambridge Philosophical Society. 80 (2): 227–250. doi:10.1017/s1464793104006657. PMID 15921050. S2CID 18866824.
  7. ^ Ohno S (1972). "So much "junk" DNA in our genome". Brookhaven Symposia in Biology. 23: 366–370. PMID 5065367.
  8. ^ Orgel LE, Crick FH, Sapienza C (December 1980). "Selfish DNA". Nature. 288 (5792): 645–6. Bibcode:1980Natur.288..645O. doi:10.1038/288645a0. PMID 7453798. S2CID 4370178.
  9. ^ Palazzo AF, Gregory TR (May 2014). "The case for junk DNA". PLOS Genetics. 10 (5): e1004351. doi:10.1371/journal.pgen.1004351. PMC 4014423. PMID 24809441.
  10. ^ Joly-Lopez Z, Bureau TE (April 2018). "Exaptation of transposable element coding sequences". Current Opinion in Genetics & Development. 49: 34–42. doi:10.1016/j.gde.2018.02.011. PMID 29525543.
  11. ^ "Tandem Repeat". Genome.gov. Retrieved 2022-09-30.
  12. ^ Sznajder ŁJ, Swanson MS (July 2019). "Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy". International Journal of Molecular Sciences. 20 (13): 3365. doi:10.3390/ijms20133365. PMC 6651174. PMID 31323950.
  13. ^ "Minisatellite Repeats (MeSH Descriptor Data 2024)". Medical Subject Headings. National Library of Medicine. D018598.
  14. ^ a b Wahls WP (1998). "Meiotic recombination hotspots: shaping the genome and insights into hypervariable minisatellite DNA change". Current Topics in Developmental Biology. 37: 37–75. doi:10.1016/s0070-2153(08)60171-4. ISBN 9780121531379. PMC 3151733. PMID 9352183.
  15. ^ Janssen A, Colmenares SU, Karpen GH (October 2018). "Heterochromatin: Guardian of the Genome". Annual Review of Cell and Developmental Biology. 34 (1): 265–288. doi:10.1146/annurev-cellbio-100617-062653. PMID 30044650. S2CID 51718804.
  16. ^ a b Qi J, Shafer RH (2005-06-02). "Covalent ligation studies on the human telomere quadruplex". Nucleic Acids Research. 33 (10): 3185–92. doi:10.1093/nar/gki632. PMC 1142406. PMID 15933211.
  17. ^ "Centromere". Genome.gov. Retrieved 2022-09-30.
  18. ^ Miga KH (September 2015). "Completing the human genome: the progress and challenge of satellite DNA assembly". Chromosome Research. 23 (3): 421–6. doi:10.1007/s10577-015-9488-2. PMID 26363799. S2CID 15229421.
  19. ^ Padeken J, Zeller P, Gasser SM (April 2015). "Repeat DNA in genome organization and stability". Current Opinion in Genetics & Development. Genome architecture and expression. 31: 12–19. doi:10.1016/j.gde.2015.03.009. PMID 25917896.
  20. ^ "Interspersed repetitive sequences - Latest research and news | Nature". www.nature.com. Retrieved 2022-09-30.
  21. ^ a b c d Wicker T, Sabot F, Hua-Van A, Bennetzen JL, Capy P, Chalhoub B, et al. (December 2007). "A unified classification system for eukaryotic transposable elements". Nature Reviews. Genetics. 8 (12): 973–982. doi:10.1038/nrg2165. PMID 17984973. S2CID 32132898.
  22. ^ a b c d e Nicolau M, Picault N, Moissiard G (October 2021). "The Evolutionary Volte-Face of Transposable Elements: From Harmful Jumping Genes to Major Drivers of Genetic Innovation". Cells. 10 (11): 2952. doi:10.3390/cells10112952. PMC 8616336. PMID 34831175.
  23. ^ a b Kramerov DA, Vassetzky NS (2011). "SINEs". Wiley Interdisciplinary Reviews. RNA. 2 (6): 772–786. doi:10.1002/wrna.91. PMID 21976282. S2CID 222199613.
  24. ^ Lee HE, Ayarpadikannan S, Kim HS (2015). "Role of transposable elements in genomic rearrangement, evolution, gene regulation and epigenetics in primates". Genes & Genetic Systems. 90 (5): 245–257. doi:10.1266/ggs.15-00016. PMID 26781081.
  25. ^ Mangiavacchi A, Liu P, Della Valle F, Orlando V (July 2021). "New insights into the functional role of retrotransposon dynamics in mammalian somatic cells". Cellular and Molecular Life Sciences. 78 (13): 5245–56. doi:10.1007/s00018-021-03851-5. PMC 8257530. PMID 33990851.
  26. ^ Ichiyanagi K (2013). "Epigenetic regulation of transcription and possible functions of mammalian short interspersed elements, SINEs". Genes & Genetic Systems. 88 (1): 19–29. doi:10.1266/ggs.88.19. PMID 23676707.
  27. ^ a b Lebel EG, Masson J, Bogucki A, Paszkowski J (January 1993). "Stress-induced intrachromosomal recombination in plant somatic cells". Proc Natl Acad Sci U S A. 90 (2): 422–6. Bibcode:1993PNAS...90..422L. doi:10.1073/pnas.90.2.422. PMC 45674. PMID 11607349.
  28. ^ Pearson CE, Zorbas H, Price GB, Zannis-Hadjopoulos M (October 1996). "Inverted repeats, stem-loops, and cruciforms: significance for initiation of DNA replication". Journal of Cellular Biochemistry. 63 (1): 1–22. doi:10.1002/(SICI)1097-4644(199610)63:1<1::AID-JCB1>3.0.CO;2-3. eISSN 1097-4644. PMID 8891900. S2CID 22204780.
  29. ^ a b Usdin K, House NC, Freudenreich CH (22 January 2015). "Repeat instability during DNA repair: Insights from model systems". Critical Reviews in Biochemistry and Molecular Biology. 50 (2): 142–167. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
  30. ^ a b Massey TH, Jones L (January 2018). "The central role of DNA damage and repair in CAG repeat diseases". Disease Models & Mechanisms. 11 (1): dmm031930. doi:10.1242/dmm.031930. PMC 5818082. PMID 29419417.
  31. ^ Cattaneo E, Zuccato C, Tartari M (December 2005). "Normal huntingtin function: an alternative approach to Huntington's disease". Nature Reviews. Neuroscience. 6 (12): 919–930. doi:10.1038/nrn1806. PMID 16288298. S2CID 10119487.
  32. ^ Maiuri T, Mocle AJ, Hung CL, Xia J, van Roon-Mom WM, Truant R (January 2017). "Huntingtin is a scaffolding protein in the ATM oxidative DNA damage response complex". Human Molecular Genetics. 26 (2): 395–406. doi:10.1093/hmg/ddw395. PMID 28017939.
  33. ^ Schulte J, Littleton JT (January 2011). "The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology". Current Trends in Neurology. 5: 65–78. PMC 3237673. PMID 22180703.
  34. ^ Penagarikano O, Mulle JG, Warren ST (2007-09-01). "The pathophysiology of fragile x syndrome". Annual Review of Genomics and Human Genetics. 8 (1): 109–129. doi:10.1146/annurev.genom.8.080706.092249. PMID 17477822.
  35. ^ Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB, Moine H, Kooy RF, et al. (September 2017). "Fragile X syndrome". Nature Reviews. Disease Primers. 3 (1): 17065. doi:10.1038/nrdp.2017.65. PMID 28960184. S2CID 583204.
  36. ^ a b Abugable AA, Morris JL, Palminha NM, Zaksauskaite R, Ray S, El-Khamisy SF (September 2019). "DNA repair and neurological disease: From molecular understanding to the development of diagnostics and model organisms". DNA Repair. 81: 102669. doi:10.1016/j.dnarep.2019.102669. PMID 31331820.
  37. ^ Honti V, Vécsei L (June 2005). "Genetic and molecular aspects of spinocerebellar ataxias". Neuropsychiatric Disease and Treatment. 1 (2): 125–133. doi:10.2147/nedt.1.2.125.61044. PMC 2413192. PMID 18568057.
  38. ^ Bürk K (2017). "Friedreich Ataxia: current status and future prospects". Cerebellum & Ataxias. 4 (1): 4. doi:10.1186/s40673-017-0062-x. PMC 5383992. PMID 28405347.
  39. ^ Mazzara PG, Muggeo S, Luoni M, Massimino L, Zaghi M, Valverde PT, et al. (August 2020). "Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons". Nature Communications. 11 (1): 4178. Bibcode:2020NatCo..11.4178M. doi:10.1038/s41467-020-17954-3. PMC 7442818. PMID 32826895.
  40. ^ Hahn C, Salajegheh MK (January 2016). "Myotonic disorders: A review article". Iranian Journal of Neurology. 15 (1): 46–53. PMC 4852070. PMID 27141276.
  41. ^ van Blitterswijk M, DeJesus-Hernandez M, Rademakers R (December 2012). "How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?". Current Opinion in Neurology. 25 (6): 689–700. doi:10.1097/WCO.0b013e32835a3efb. PMC 3923493. PMID 23160421.
  42. ^ a b De Bustos A, Cuadrado A, Jouve N (November 2016). "Sequencing of long stretches of repetitive DNA". Scientific Reports. 6 (1): 36665. Bibcode:2016NatSR...636665D. doi:10.1038/srep36665. PMC 5098217. PMID 27819354.
  43. ^ Slotkin RK (1 May 2018). "The case for not masking away repetitive DNA". Mobile DNA. 9 (1): 15. doi:10.1186/s13100-018-0120-9. PMC 5930866. PMID 29743957.
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