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GeezerVison is showing en.wikipedia.org — Base J - Wikipedia

Base J
Names
IUPAC name
5-[(β-D-Glucopyranosyloxy)methyl]pyrimidine-2,4(1H,3H)-dione
Systematic IUPAC name
5-({[(2R,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)pyrimidine-2,4(1H,3H)-dione
Other names
β-D-Glucosyl-5-hydroxymethyluracil
β-D-Glucosyl-hydroxymethyluracil
Identifiers
CAS Number
  • 53910-89-7
3D model (JSmol)
  • Interactive image
ChemSpider
  • 32742278
PubChem CID
  • 129852278
UNII
  • 979DWB8FWS checkY
InChI
  • InChI=1S/C11H16N2O8/c14-2-5-6(15)7(16)8(17)10(21-5)20-3-4-1-12-11(19)13-9(4)18/h1,5-8,10,14-17H,2-3H2,(H2,12,13,18,19)/t5-,6-,7+,8-,10-/m1/s1
    Key: SUDBRAWXUGTELR-HPFNVAMJSA-N
  • InChI=1/C11H16N2O8/c14-2-5-6(15)7(16)8(17)10(21-5)20-3-4-1-12-11(19)13-9(4)18/h1,5-8,10,14-17H,2-3H2,(H2,12,13,18,19)/t5-,6-,7+,8-,10-/m1/s1
    Key: SUDBRAWXUGTELR-HPFNVAMJBD
SMILES
  • c1c(c(=O)[nH]c(=O)[nH]1)CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
Properties
Chemical formula
C11H16N2O8
Molar mass 304.255 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

β-D-Glucopyranosyloxymethyluracil or base J is a hypermodified nucleobase found in the DNA of kinetoplastids including the human pathogenic trypanosomes. It was discovered in 1993, in the trypanosome Trypanosoma brucei and was the first hypermodified nucleobase found in eukaryotic DNA; it has since been found in other kinetoplastids, including Leishmania.[1] Within these organisms Base J acts as a RNA polymerase II transcription terminator, with its removal in knockout cells being accompanied by a massive read-through at RNA polymerase II termination sites, which ultimately proves lethal to the cell.[2][3]

Base J is formed by the initial hydroxylation of thymidine and the subsequent glycosylation by a glycosyltransferase.[4]

The biosynthesis of base J. A: thymidine hydroxylase; B: beta-glucosyltranferase; 1: dT (desoxy thymidine); 2: HOCH3dU; 3: dJ

References

  1. ↑ Borst, Piet; Sabatini, Robert (October 2008). "Base J: Discovery, Biosynthesis, and Possible Functions". Annual Review of Microbiology. 62 (1): 235–251. doi:10.1146/annurev.micro.62.081307.162750. PMID 18729733.
  2. ↑ van Luenen, Henri G.A.M.; Farris, Carol; Jan, Sabrina; Genest, Paul-Andre; Tripathi, Pankaj; Velds, Arno; Kerkhoven, Ron M.; Nieuwland, Marja; Haydock, Andrew; Ramasamy, Gowthaman; Vainio, Saara; Heidebrecht, Tatjana; Perrakis, Anastassis; Pagie, Ludo; van Steensel, Bas; Myler, Peter J.; Borst, Piet (August 2012). "Glucosylated Hydroxymethyluracil, DNA Base J, Prevents Transcriptional Readthrough in Leishmania". Cell. 150 (5): 909–921. doi:10.1016/j.cell.2012.07.030. PMC 3684241. PMID 22939620.
  3. ↑ Hazelbaker, Dane Z.; Buratowski, Stephen (November 2012). "Transcription: Base J Blocks the Way". Current Biology. 22 (22): R960–R962. Bibcode:2012CBio...22.R960H. doi:10.1016/j.cub.2012.10.010. PMC 3648658. PMID 23174300.
  4. ↑ Bullard, Whitney; Lopes da Rosa-Spiegler, Jessica; Liu, Shuo; Wang, Yinsheng; Sabatini, Robert (July 2014). "Identification of the Glucosyltransferase That Converts Hydroxymethyluracil to Base J in the Trypanosomatid Genome". Journal of Biological Chemistry. 289 (29): 20273–20282. doi:10.1074/jbc.M114.579821. PMC 4106341. PMID 24891501.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Base_J&oldid=1372313844"
Categories:
  • Nucleobases
  • Thymine derivatives
  • Glucosides
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