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Wikipedia

Cytosine

Cytosine (/ˈstəˌsn, -ˌzn, -ˌsɪn/[2][3]) (symbol C or Cyt) is one of the four nucleobases found in DNA and RNA, along with adenine, guanine, and thymine (uracil in RNA). It is a pyrimidine derivative, with a heterocyclic aromatic ring and two substituents attached (an amine group at position 4 and a keto group at position 2). The nucleoside of cytosine is cytidine. In Watson-Crick base pairing, it forms three hydrogen bonds with guanine.

Cytosine
Names
Preferred IUPAC name
4-Aminopyrimidin-2(1H)-one
Other names
4-Amino-1H-pyrimidine-2-one
Identifiers
  • 71-30-7 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:16040 Y
ChEMBL
  • ChEMBL15913 Y
ChemSpider
  • 577 Y
ECHA InfoCard 100.000.681
KEGG
  • C00380 Y
MeSH Cytosine
  • 597
UNII
  • 8J337D1HZY Y
  • DTXSID4044456
  • InChI=1S/C4H5N3O/c5-3-1-2-6-4(8)7-3/h1-2H,(H3,5,6,7,8) Y
    Key: OPTASPLRGRRNAP-UHFFFAOYSA-N Y
  • InChI=1/C4H5N3O/c5-3-1-2-6-4(8)7-3/h1-2H,(H3,5,6,7,8)
    Key: OPTASPLRGRRNAP-UHFFFAOYAY
  • O=C1Nccc(N)n1
Properties
C4H5N3O
Molar mass 111.10 g/mol
Density 1.55 g/cm3 (calculated)
Melting point 320 to 325 °C (608 to 617 °F; 593 to 598 K) (decomposes)
Acidity (pKa) 4.45 (secondary), 12.2 (primary)[1]
-55.8·10−6 cm3/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

History edit

Cytosine was discovered and named by Albrecht Kossel and Albert Neumann in 1894 when it was hydrolyzed from calf thymus tissues.[4][5] A structure was proposed in 1903, and was synthesized (and thus confirmed) in the laboratory in the same year.

In 1998, cytosine was used in an early demonstration of quantum information processing when Oxford University researchers implemented the Deutsch–Jozsa algorithm on a two qubit nuclear magnetic resonance quantum computer (NMRQC).[6]

In March 2015, NASA scientists reported the formation of cytosine, along with uracil and thymine, from pyrimidine under the space-like laboratory conditions, which is of interest because pyrimidine has been found in meteorites although its origin is unknown.[7]

Chemical reactions edit

 
Cytosine
Cytosine and guanine with the direction of hydrogen bonding indicated (arrow points positive to negative charge).
Methylation of cytosine occurs on carbon number 5.

Cytosine can be found as part of DNA, as part of RNA, or as a part of a nucleotide. As cytidine triphosphate (CTP), it can act as a co-factor to enzymes, and can transfer a phosphate to convert adenosine diphosphate (ADP) to adenosine triphosphate (ATP).

In DNA and RNA, cytosine is paired with guanine. However, it is inherently unstable, and can change into uracil (spontaneous deamination). This can lead to a point mutation if not repaired by the DNA repair enzymes such as uracil glycosylase, which cleaves a uracil in DNA.

Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase or be methylated and hydroxylated to make 5-hydroxymethylcytosine. The difference in rates of deamination of cytosine and 5-methylcytosine (to uracil and thymine) forms the basis of bisulfite sequencing.[8]

Biological function edit

When found third in a codon of RNA, cytosine is synonymous with uracil, as they are interchangeable as the third base. When found as the second base in a codon, the third is always interchangeable. For example, UCU, UCC, UCA and UCG are all serine, regardless of the third base.

Active enzymatic deamination of cytosine or 5-methylcytosine by the APOBEC family of cytosine deaminases could have both beneficial and detrimental implications on various cellular processes as well as on organismal evolution.[9] The implications of deamination on 5-hydroxymethylcytosine, on the other hand, remains less understood.

Theoretical aspects edit

Until October 2021, Cytosine had not been found in meteorites, which suggested the first strands of RNA and DNA had to look elsewhere to obtain this building block. Cytosine likely formed within some meteorite parent bodies, however did not persist within these bodies due to an effective deamination reaction into uracil.[10]

In October 2021, Cytosine was announced as having been found in meteorites by researchers in a joint Japan/NASA project, that used novel methods of detection which avoided damaging nucleotides as they were extracted from meteorites.[11]

References edit

  1. ^ Dawson, R.M.C.; et al. (1959). Data for Biochemical Research. Oxford: Clarendon Press.
  2. ^ "Cytosine". Dictionary.com Unabridged (Online). n.d.
  3. ^ "Cytosine". Merriam-Webster.com Dictionary.
  4. ^ A. Kossel and Albert Neumann (1894) "Darstellung und Spaltungsprodukte der Nucleïnsäure (Adenylsäure)" (Preparation and cleavage products of nucleic acids (adenic acid)), Berichte der Deutschen Chemischen Gesellschaft zu Berlin, 27 : 2215–2222. The name "cytosine" is coined on page 2219: " … ein Produkt von basischen Eigenschaften, für welches wir den Namen "Cytosin" vorschlagen." ( … a product with basic properties, for which we suggest the name "cytosine".)
  5. ^ Kossel, A.; Steudel, H. Z. (1903). "Weitere Untersuchungen über das Cytosin". Physiol. Chem. 38 (1–2): 49–59. doi:10.1515/bchm2.1903.38.1-2.49.
  6. ^ Jones, J.A.; M. Mosca (1998-08-01). . J. Chem. Phys. 109 (5): 1648–1653. arXiv:quant-ph/9801027. Bibcode:1998JChPh.109.1648J. doi:10.1063/1.476739. S2CID 19348964. Archived from the original on 2008-06-12. Retrieved 2007-10-18.
  7. ^ Marlaire, Ruth (3 March 2015). . NASA. Archived from the original on 5 March 2015. Retrieved 5 March 2015.
  8. ^ Hayatsu, Hikoya (2008). "Discovery of bisulfite-mediated cytosine conversion to uracil, the key reaction for DNA methylation analysis — A personal account". Proceedings of the Japan Academy. Series B, Physical and Biological Sciences. 84 (8): 321–330. Bibcode:2008PJAB...84..321H. doi:10.2183/pjab.84.321. ISSN 0386-2208. PMC 3722019. PMID 18941305.
  9. ^ Chahwan R.; Wontakal S.N.; Roa S. (2010). "Crosstalk between genetic and epigenetic information through cytosine deamination". Trends in Genetics. 26 (10): 443–448. doi:10.1016/j.tig.2010.07.005. PMID 20800313.
  10. ^ Tasker, Elizabeth. "Did the Seeds of Life Come from Space?". Scientific American Blog Network. Retrieved 2016-11-24.
  11. ^ Yasuhiro Oba; Yoshinori Takano; Yoshihiro Furukawa; Toshiki Koga; Daniel P. Glavin; Jason P. Dworkin; Hiroshi Naraoka. "Identifying the wide diversity of extraterrestrial purine and pyrimidine nucleobases in carbonaceous meteorites". The Journal of Nature Communications. Nature.com. Retrieved 7 July 2022.

External links and citations edit

  • EINECS number 200-749-5
  • Shapiro R (1999). "Prebiotic cytosine synthesis: a critical analysis and implications for the origin of life". Proc. Natl. Acad. Sci. U.S.A. 96 (8): 4396–401. Bibcode:1999PNAS...96.4396S. doi:10.1073/pnas.96.8.4396. PMC 16343. PMID 10200273.

cytosine, confused, with, cytokine, cytidine, cysteine, cystine, cytisine, symbol, four, nucleobases, found, along, with, adenine, guanine, thymine, uracil, pyrimidine, derivative, with, heterocyclic, aromatic, ring, substituents, attached, amine, group, posit. Not to be confused with cytokine cytidine cysteine cystine or cytisine Cytosine ˈ s aɪ t e ˌ s iː n ˌ z iː n ˌ s ɪ n 2 3 symbol C or Cyt is one of the four nucleobases found in DNA and RNA along with adenine guanine and thymine uracil in RNA It is a pyrimidine derivative with a heterocyclic aromatic ring and two substituents attached an amine group at position 4 and a keto group at position 2 The nucleoside of cytosine is cytidine In Watson Crick base pairing it forms three hydrogen bonds with guanine Cytosine NamesPreferred IUPAC name 4 Aminopyrimidin 2 1H oneOther names 4 Amino 1H pyrimidine 2 oneIdentifiersCAS Number 71 30 7 Y3D model JSmol Interactive imageChEBI CHEBI 16040 YChEMBL ChEMBL15913 YChemSpider 577 YECHA InfoCard 100 000 681KEGG C00380 YMeSH CytosinePubChem CID 597UNII 8J337D1HZY YCompTox Dashboard EPA DTXSID4044456InChI InChI 1S C4H5N3O c5 3 1 2 6 4 8 7 3 h1 2H H3 5 6 7 8 YKey OPTASPLRGRRNAP UHFFFAOYSA N YInChI 1 C4H5N3O c5 3 1 2 6 4 8 7 3 h1 2H H3 5 6 7 8 Key OPTASPLRGRRNAP UHFFFAOYAYSMILES O C1Nccc N n1PropertiesChemical formula C4H5N3OMolar mass 111 10 g molDensity 1 55 g cm3 calculated Melting point 320 to 325 C 608 to 617 F 593 to 598 K decomposes Acidity pKa 4 45 secondary 12 2 primary 1 Magnetic susceptibility x 55 8 10 6 cm3 molExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox references Contents 1 History 2 Chemical reactions 3 Biological function 4 Theoretical aspects 5 References 6 External links and citationsHistory editCytosine was discovered and named by Albrecht Kossel and Albert Neumann in 1894 when it was hydrolyzed from calf thymus tissues 4 5 A structure was proposed in 1903 and was synthesized and thus confirmed in the laboratory in the same year In 1998 cytosine was used in an early demonstration of quantum information processing when Oxford University researchers implemented the Deutsch Jozsa algorithm on a two qubit nuclear magnetic resonance quantum computer NMRQC 6 In March 2015 NASA scientists reported the formation of cytosine along with uracil and thymine from pyrimidine under the space like laboratory conditions which is of interest because pyrimidine has been found in meteorites although its origin is unknown 7 Chemical reactions edit nbsp Cytosine nbsp GuanineCytosine and guanine with the direction of hydrogen bonding indicated arrow points positive to negative charge Methylation of cytosine occurs on carbon number 5 Cytosine can be found as part of DNA as part of RNA or as a part of a nucleotide As cytidine triphosphate CTP it can act as a co factor to enzymes and can transfer a phosphate to convert adenosine diphosphate ADP to adenosine triphosphate ATP In DNA and RNA cytosine is paired with guanine However it is inherently unstable and can change into uracil spontaneous deamination This can lead to a point mutation if not repaired by the DNA repair enzymes such as uracil glycosylase which cleaves a uracil in DNA Cytosine can also be methylated into 5 methylcytosine by an enzyme called DNA methyltransferase or be methylated and hydroxylated to make 5 hydroxymethylcytosine The difference in rates of deamination of cytosine and 5 methylcytosine to uracil and thymine forms the basis of bisulfite sequencing 8 Biological function editWhen found third in a codon of RNA cytosine is synonymous with uracil as they are interchangeable as the third base When found as the second base in a codon the third is always interchangeable For example UCU UCC UCA and UCG are all serine regardless of the third base Active enzymatic deamination of cytosine or 5 methylcytosine by the APOBEC family of cytosine deaminases could have both beneficial and detrimental implications on various cellular processes as well as on organismal evolution 9 The implications of deamination on 5 hydroxymethylcytosine on the other hand remains less understood Theoretical aspects editUntil October 2021 Cytosine had not been found in meteorites which suggested the first strands of RNA and DNA had to look elsewhere to obtain this building block Cytosine likely formed within some meteorite parent bodies however did not persist within these bodies due to an effective deamination reaction into uracil 10 In October 2021 Cytosine was announced as having been found in meteorites by researchers in a joint Japan NASA project that used novel methods of detection which avoided damaging nucleotides as they were extracted from meteorites 11 References edit Dawson R M C et al 1959 Data for Biochemical Research Oxford Clarendon Press Cytosine Dictionary com Unabridged Online n d Cytosine Merriam Webster com Dictionary A Kossel and Albert Neumann 1894 Darstellung und Spaltungsprodukte der Nucleinsaure Adenylsaure Preparation and cleavage products of nucleic acids adenic acid Berichte der Deutschen Chemischen Gesellschaft zu Berlin 27 2215 2222 The name cytosine is coined on page 2219 ein Produkt von basischen Eigenschaften fur welches wir den Namen Cytosin vorschlagen a product with basic properties for which we suggest the name cytosine Kossel A Steudel H Z 1903 Weitere Untersuchungen uber das Cytosin Physiol Chem 38 1 2 49 59 doi 10 1515 bchm2 1903 38 1 2 49 Jones J A M Mosca 1998 08 01 Implementation of a quantum algorithm on a nuclear magnetic resonance quantum computer J Chem Phys 109 5 1648 1653 arXiv quant ph 9801027 Bibcode 1998JChPh 109 1648J doi 10 1063 1 476739 S2CID 19348964 Archived from the original on 2008 06 12 Retrieved 2007 10 18 Marlaire Ruth 3 March 2015 NASA Ames Reproduces the Building Blocks of Life in Laboratory NASA Archived from the original on 5 March 2015 Retrieved 5 March 2015 Hayatsu Hikoya 2008 Discovery of bisulfite mediated cytosine conversion to uracil the key reaction for DNA methylation analysis A personal account Proceedings of the Japan Academy Series B Physical and Biological Sciences 84 8 321 330 Bibcode 2008PJAB 84 321H doi 10 2183 pjab 84 321 ISSN 0386 2208 PMC 3722019 PMID 18941305 Chahwan R Wontakal S N Roa S 2010 Crosstalk between genetic and epigenetic information through cytosine deamination Trends in Genetics 26 10 443 448 doi 10 1016 j tig 2010 07 005 PMID 20800313 Tasker Elizabeth Did the Seeds of Life Come from Space Scientific American Blog Network Retrieved 2016 11 24 Yasuhiro Oba Yoshinori Takano Yoshihiro Furukawa Toshiki Koga Daniel P Glavin Jason P Dworkin Hiroshi Naraoka Identifying the wide diversity of extraterrestrial purine and pyrimidine nucleobases in carbonaceous meteorites The Journal of Nature Communications Nature com Retrieved 7 July 2022 External links and citations edit nbsp Wikimedia Commons has media related to Cytosine Cytosine MS Spectrum EINECS number 200 749 5 Shapiro R 1999 Prebiotic cytosine synthesis a critical analysis and implications for the origin of life Proc Natl Acad Sci U S A 96 8 4396 401 Bibcode 1999PNAS 96 4396S doi 10 1073 pnas 96 8 4396 PMC 16343 PMID 10200273 Retrieved from https en wikipedia org w index php title Cytosine amp oldid 1193265316, wikipedia, wiki, book, books, library,

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