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5-Hydroxymethylcytosine

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5-Hydroxymethylcytosine
Skeletal formula of 5-hydroxymethylcytosine
Ball-and-stick model of the 5-hydroxymethylcytosine molecule
Names
Preferred IUPAC name
4-Amino-5-(hydroxymethyl)pyrimidin-2(1H)-one
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C5H7N3O2/c6-4-3(2-9)1-7-5(10)8-4/h1,9H,2H2,(H3,6,7,8,10) checkY
    Key: RYVNIFSIEDRLSJ-UHFFFAOYSA-N checkY
  • InChI=1/C5H7N3O2/c6-4-3(2-9)1-7-5(10)8-4/h1,9H,2H2,(H3,6,7,8,10)
    Key: RYVNIFSIEDRLSJ-UHFFFAOYAT
  • C1=NC(=O)NC(=C1CO)N
  • O=C1/N=C\C(=C(\N)N1)CO
Properties
C5H7N3O2
Molar mass 141.13 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

5-Hydroxymethylcytosine (5hmC) is a DNA pyrimidine nitrogen base derived from cytosine. It is potentially important in epigenetics, because the hydroxymethyl group on the cytosine can possibly switch a gene on and off. It was first seen in bacteriophages in 1952.[1][2] However, in 2009 it was found to be abundant in human and mouse brains,[3] as well as in embryonic stem cells.[4] In mammals, it can be generated by oxidation of 5-methylcytosine, a reaction mediated by TET enzymes. Its molecular formula is C5H7N3O2.[5]

Localization

Every mammalian cell seems to contain 5-Hydroxymethylcytosine, but the levels vary significantly depending on the cell type. The highest levels are found in neuronal cells of the central nervous system.[6][7][8] The amount of hydroxymethylcytosine increases with age, as shown in mouse hippocampus and cerebellum.[6][9]

Function

The exact function of this nitrogen base is still not fully elucidated, but it is thought that it may regulate gene expression or prompt DNA demethylation. This hypothesis is supported by the fact that artificial DNA that contains 5-hydroxymethylcytosines (5hmC) can be converted into unmodified cytosines once introduced into mammalian cells.[10] Moreover, 5hmC is highly enriched in primordial germ cells, where it apparently plays a role in global DNA demethylation.[11] Additionally, 5-Formylcytosine, an oxidation product of 5-Hydroxymethylcytosine and possible intermediate of an oxidative demethylation pathway was detected in DNA from embryonic stem cells,[12] although no significant amounts of these putative demethylation intermediates could be detected in mouse tissue.[8] 5-Hydroxymethylcytosine may be especially important in the central nervous system, as it is found in very high levels there.[8] Reduction in the 5-Hydroxymethylcytosine levels have been found associated with impaired self-renewal in embryonic stem cells.[13] 5-Hydroxymethylcytosine is also associated with labile, unstable nucleosomes which are frequently repositioned during cell differentiation.[14]

The accumulation of 5-hydroxymethylcytosine (5hmC) in post-mitotic neurons is associated with “functional demethylation” that facilitates transcription and gene expression.[15] The term “demethylation,” as applied to neurons, ordinarily refers to the replacement of 5-methylcytosine (5mC) by cytosine in DNA that can occur through a series of reactions involving a TET enzyme as well as enzymes of the DNA base excision repair pathway (see Epigenetics in learning and memory). “Demethylation” of 5mC in DNA most often results in the promotion of expression of genes with neuronal activities. “Functional demethylation” refers to the replacement of 5mC by 5hmC, ordinarily a single-step TET-mediated reaction, that also facilitates gene expression, an effect similar to that of “demethylation.”

Bacteria and phages

Phages probably evolved to use 5hmC to avoid recognition by most restriction enzymes in bacteria. The T4 phage uses 5hmC exclusively during replication, adding glycosylation to the hydroxyl group to further complicate the moiety.[16] Some bacteria have in turn evolved restriction enzymes specific for sites containing 5hmC. One prominent example is PvuRts1I, originally identified in 1994.[17]

5hmC in T4 is produced by genome protein 42, deoxycytidylate 5-hydroxymethyltransferase (P08773; EC 2.1.2.8). The glycosylation reactions are known as EC 2.4.1.26, EC 2.4.1.27, and EC 2.4.1.28.

History

5-Hydroxymethylcytosine was observed by Skirmantas Kriaucionis, an associate at the Heintz lab, who was looking for levels of 5-methylcytosine in two different neuron types. He discovered a significant amount of an unknown substance instead, and after conducting several tests, identified it as being 5-hydroxymethylcytosine.[18]

The lab of L. Aravind used bioinformatic tools to predict that the Tet family of enzymes would likely oxidize 5-methylcytosine to 5-hydroxymethylcytosine.[19] This was demonstrated in vitro and in live human and mouse cells by scientists working in the labs of Anjana Rao and David R. Liu.

5-Hydroxymethylcytosine was originally observed in mammals in 1972 by R. Yura,[20] but this initial finding is dubious. Yura found 5-hmC present at extremely high levels in rat brain and liver, completely supplanting 5-methylcytosine. This contradicts all research conducted on mammalian DNA composition conducted before and since, including the Heintz and Rao papers, and another group was unable to reproduce Yura's result.[21]

With the discovery of 5-hydroxymethylcytosine some concerns have been raised regarding DNA methylation studies using the bisulfite sequencing technique.[22] 5-hydroxymethylcytosine has been shown to behave like its precursor, 5-methylcytosine, in bisulfite conversion experiments.[23] Therefore, bisulfite sequencing data may need to be revisited to verify whether the detected modified base is 5-methylcytosine or 5-hydroxymethylcytosine. In 2012 the lab of Chuan He discovered a method to solve the problems of 5-hydroxymethylcytosine being detected as 5-methylcytosine in normal bisulfite conversion experiments using the oxidative properties of the Tet-family of enzymes, this method has been termed TAB-seq.[24][25]

In June 2020, Oxford Nanopore added a hydroxymethyl cytosine detection model to their research basecaller, rerio, allowing old signal-level data from any R9+ nanopore runs to be re-called to identify 5hmC. [26]

References

  1. ^ Warren RA (1980). "Modified bases in bacteriophage DNAs". Annu. Rev. Microbiol. 34: 137–158. doi:10.1146/annurev.mi.34.100180.001033. PMID 7002022.
  2. ^ Wyatt GR, Cohen SS (December 1952). "A new pyrimidine base from bacteriophage nucleic acids". Nature. 170 (4338): 1072–1073. Bibcode:1952Natur.170.1072W. doi:10.1038/1701072a0. PMID 13013321. S2CID 4277592.
  3. ^ Kriaucionis S, Heintz N (May 2009). "The nuclear DNA base 5-hydroxymethylcytosine is present in Purkinje neurons and the brain". Science. 324 (5929): 929–930. Bibcode:2009Sci...324..929K. doi:10.1126/science.1169786. PMC 3263819. PMID 19372393.
  4. ^ Tahiliani M, et al. (May 2009). "Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1" (PDF). Science. 324 (5929): 930–935. Bibcode:2009Sci...324..930T. doi:10.1126/science.1170116. PMC 2715015. PMID 19372391.
  5. ^ 5-Hydroxymethylcytosine Archived 2017-09-04 at the Wayback Machine, nextbio.com
  6. ^ a b Münzel M, et al. (July 2010). "Quantification of the Sixth DNA Base Hydroxymethylcytosine in the Brain". Angew. Chem. Int. Ed. 49 (31): 5375–5377. doi:10.1002/anie.201002033. PMID 20583021.
  7. ^ Szwagierczak A, et al. (October 2010). "Sensitive Enzymatic Quantification of 5-Hydroxymethylcytosine in Genomic DNA". Nucleic Acids Res. 38 (19): e181. doi:10.1093/nar/gkq684. PMC 2965258. PMID 20685817.
  8. ^ a b c Globisch D, et al. (December 2010). Croft AK (ed.). "Tissue Distribution of 5-Hydroxymethylcytosine and Search for Active Demethylation Intermediates". PLOS ONE. 5 (12): e15367. Bibcode:2010PLoSO...515367G. doi:10.1371/journal.pone.0015367. PMC 3009720. PMID 21203455.
  9. ^ Song C-X, et al. (December 2010). "Selective chemical labeling reveals the genome-wide distribution of 5-hydroxymethylcytosine". Nat. Biotechnol. 29 (1): 68–72. doi:10.1038/nbt.1732. PMC 3107705. PMID 21151123.
  10. ^ Guo JU, Su Y, Zhong C, Ming Gl, Song H (1 April 2011). "Hydroxylation of 5-Methylcytosine by TET1 Promotes Active DNA Demethylation in the Adult Brain". Cell. 145 (3): 423–434. doi:10.1016/j.cell.2011.03.022. PMC 3088758. PMID 21496894.
  11. ^ Hackett JA, Sengupta R, Zylicz JJ, Murakami K, Lee C, Down T, Surani MA (2012-12-06). "Germline DNA demethylation dynamics and imprint erasure through 5-hydroxymethylcytosine". Science. 339 (6118): 448–52. doi:10.1126/science.1229277. PMC 3847602. PMID 23223451.
  12. ^ Pfaffeneder T, Hackner B, Truss M, Münzel M, Müller M, Deiml CA, Hagemeier C, Carell T (30 June 2011). "The Discovery of 5-Formylcytosine in Embryonic Stem Cell DNA". Angew. Chem. Int. Ed. 50 (31): 7008–7012. doi:10.1002/anie.201103899. PMID 21721093.
  13. ^ Freudenberg JM, Ghosh S, Lackford BL, Yellaboina S, Zheng X, Li R, Cuddapah S, Wade PA, Hu G, Jothi R (April 2012). "Acute depletion of Tet1-dependent 5-hydroxymethylcytosine levels impairs LIF/Stat3 signaling and results in loss of embryonic stem cell identity". Nucleic Acids Research. 40 (8): 3364–3377. doi:10.1093/nar/gkr1253. PMC 3333871. PMID 22210859.
  14. ^ Teif V, Beshnova DA, Vainshtein Y, Marth C, Mallm JP, Höfer T, Rippe K (8 May 2014). "Nucleosome repositioning links DNA (de)methylation and differential CTCF binding during stem cell development". Genome Research. 24 (8): 1285–1295. doi:10.1101/gr.164418.113. PMC 4120082. PMID 24812327.
  15. ^ Mellén M, Ayata P, Heintz N (Sep 2017). "5-hydroxymethylcytosine accumulation in postmitotic neurons results in functional demethylation of expressed genes". Proc Natl Acad Sci U S A. 114 (37): E7812–E7821. Bibcode:2017PNAS..114E7812M. doi:10.1073/pnas.1708044114. PMC 5604027. PMID 28847947.
  16. ^ Bryson AL, Hwang Y, Sherrill-Mix S, Wu GD, Lewis JD, Black L, Clark TA, Bushman FD, Adhya S (16 June 2015). "Covalent Modification of Bacteriophage T4 DNA Inhibits CRISPR-Cas9". mBio. 6 (3): e00648. doi:10.1128/mBio.00648-15. PMC 4471564. PMID 26081634.
  17. ^ Borgaro JG, Zhu Z (April 2013). "Characterization of the 5-hydroxymethylcytosine-specific DNA restriction endonucleases". Nucleic Acids Research. 41 (7): 4198–206. doi:10.1093/nar/gkt102. PMC 3627594. PMID 23482393.
  18. ^ A, T, G, C and What?, popsci.com
  19. ^ Iyer LM, et al. (June 2009). "Prediction of novel families of enzymes involved in oxidative and other complex modifications of bases in nucleic acids". Cell Cycle. 8 (11): 1698–1710. doi:10.4161/cc.8.11.8580. PMC 2995806. PMID 19411852.
  20. ^ Penn NW, Suwalski R, O'Riley C, Bojanowski K, Yura R (February 1972). "The presence of 5-hydroxymethylcytosine in animal deoxyribonucleic acid". Biochem. J. 126 (4): 781–790. doi:10.1042/bj1260781. PMC 1178489. PMID 4538516.
  21. ^ Kothari R, Shankar V (May 1976). "5-Methylcytosine content in the vertebrate deoxyribonucleic acids: species specificity". Journal of Molecular Evolution. 7 (4): 325–329. Bibcode:1976JMolE...7..325K. doi:10.1007/BF01743628. ISSN 0022-2844. PMID 933178. S2CID 19957320.
  22. ^ "5 hydroxymethylcytosine analysis techniques". Archived from the original on 2011-07-10. Retrieved 2011-01-14.
  23. ^ Jin SG et al. (Jun 2010) "Examination of the specificity of DNA methylation profiling techniques towards 5-methylcytosine and 5-hydroxymethylcytosine." Nucleic Acids Res. 2010 Jun 1;38(11):e125
  24. ^ Yu M, Hon GC, Szulwach KE, Song CX, Zhang L, Kim A, Li XK, Dai Q, Shen Y, Park B, Min JH, Jin P, Ren B, He C (June 2012). "Base-resolution analysis of 5-hydroxymethylcytosine in the mammalian genome". Cell. 149 (6): 1368–1380. doi:10.1016/j.cell.2012.04.027. PMC 3589129. PMID 22608086.
  25. ^ Song CX, Szulwach KE, Fu Y, Dai Q, Yi C, Li X, Li Y, Chen CH, Zhang W, Jian X, Wang J, Zhang L, Looney TJ, Zhang B, Godley LA, Hicks LM, Lahn BT, Jin P, He C (2011). "Selective chemical labeling reveals the genome-wide distribution of 5-hydroxymethylcytosine". Nat. Biotechnol. 29 (1): 68–72. doi:10.1038/nbt.1732. PMC 3107705. PMID 21151123.
  26. ^ "Added CpG (min, prom, and min 5mC+5hmC) models and some minor cleanup". nanoporetech / rerio. GitHub. Retrieved 18 June 2020.

See also

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