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{{Short description|Chemical compound of DNA and RNA}}
{{Short description|Chemical compound in nucleic acids}}
{{distinguish|cysteine|cystine|cytisine|cytidine}}
{{Distinguish|cytokine|cytidine|cysteine|cystine|cytisine}}
{{chembox
{{chembox
| Watchedfields = changed
| Watchedfields = changed
| verifiedrevid = 443557332
| verifiedrevid = 443557332
| ImageFile1 = Cytosine_chemical_structure.png
| ImageFile1 = Cytosine structure 2022.svg
| ImageSize1 = 120px
| ImageSize1 = 120px
| ImageFile2 = Cytosine-3D-balls.png
| ImageFile2 = Cytosine-3D-balls.png
| ImageSize2 = 180px
| ImageSize2 = 180px
| ImageFile3 = Cytosine-3D-vdW.png
| ImageFile3 = Cytosine-3D-vdW.png
| ImageSize3 = 150px
| ImageSize3 = 150px
| IUPACName=4-aminopyrimidin-2(1''H'')-one
| PIN = 4-Aminopyrimidin-2(1''H'')-one
| OtherNames=4-amino-1''H''-pyrimidine-2-one
| OtherNames = 4-Amino-1''H''-pyrimidine-2-one
|Section1={{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 577
| ChemSpiderID = 577
Line 21: Line 21:
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = OPTASPLRGRRNAP-UHFFFAOYSA-N
| StdInChIKey = OPTASPLRGRRNAP-UHFFFAOYSA-N
| CASNo=71-30-7
| CASNo = 71-30-7
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo_Ref = {{cascite|correct|CAS}}
| PubChem=597
| PubChem = 597
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 8J337D1HZY
| UNII = 8J337D1HZY
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 16040
| ChEBI = 16040
| SMILES = c1cnc(=O)[nH]c1N
| SMILES = O=C1Nccc(N)n1
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C00380
| KEGG = C00380
| InChI = 1/C4H5N3O/c5-3-1-2-6-4(8)7-3/h1-2H,(H3,5,6,7,8)
| InChI = 1/C4H5N3O/c5-3-1-2-6-4(8)7-3/h1-2H,(H3,5,6,7,8)
| InChIKey = OPTASPLRGRRNAP-UHFFFAOYAY
| InChIKey = OPTASPLRGRRNAP-UHFFFAOYAY
| MeSHName=Cytosine
| MeSHName = Cytosine
}}
}}
|Section2={{Chembox Properties
| Section2 = {{Chembox Properties
| Formula=C<sub>4</sub>H<sub>5</sub>N<sub>3</sub>O
| Formula=C<sub>4</sub>H<sub>5</sub>N<sub>3</sub>O
| MolarMass=111.10 g/mol
| MolarMass=111.10 g/mol
Line 47: Line 47:
| MagSus = -55.8·10<sup>−6</sup> cm<sup>3</sup>/mol
| MagSus = -55.8·10<sup>−6</sup> cm<sup>3</sup>/mol
}}
}}
|Section3={{Chembox Hazards
| Section3 = {{Chembox Hazards
| MainHazards=
| MainHazards=
| FlashPt=
| FlashPt=
Line 54: Line 54:
}}
}}


'''Cytosine''' ({{IPAc-en|ˈ|s|aɪ|t|ə|ˌ|s|iː|n|,_|-|ˌ|z|iː|n|,_|-|ˌ|s|ɪ|n}};<ref>{{Dictionary.com|Cytosine}}</ref><ref>{{MerriamWebsterDictionary|Cytosine}}</ref> '''C''') is one of the four main bases 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 [[Ketone|keto]] group at position 2). The [[nucleoside]] of cytosine is [[cytidine]]. In Watson-Crick [[base pair]]ing, it forms three hydrogen bonds with [[guanine]].
'''Cytosine''' ({{IPAc-en|ˈ|s|aɪ|t|ə|ˌ|s|iː|n|,_|-|ˌ|z|iː|n|,_|-|ˌ|s|ɪ|n}}<ref>{{Dictionary.com|Cytosine}}</ref><ref>{{MerriamWebsterDictionary|Cytosine}}</ref>) ([[nucleoside#List of nucleosides and corresponding nucleobases|symbol]] '''C''' or '''Cyt''') is one of the four [[Nucleobase|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 [[Ketone|keto]] group at position 2). The [[nucleoside]] of cytosine is [[cytidine]]. In [[Watson–Crick base pair]]ing, it forms three [[hydrogen bond]]s with [[guanine]].


==History==
==History==
Cytosine was discovered and named by [[Albrecht Kossel]] and Albert Neumann in 1894 when it was hydrolyzed from calf [[thymus]] tissues.<ref>A. Kossel and Albert Neumann (1894) [http://gallica.bnf.fr/ark:/12148/bpt6k90735d/f437.image.langEN "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".)</ref><ref>{{cite journal |author1=Kossel, A. |author2=Steudel, H. Z. | journal = Physiol. Chem. | year = 1903 | volume = 38 |issue=1–2 | pages = 49–59 | doi = 10.1515/bchm2.1903.38.1-2.49 | title = Weitere Untersuchungen über das Cytosin|url=https://zenodo.org/record/1448762 }}</ref> A structure was proposed in 1903, and was synthesized (and thus confirmed) in the laboratory in the same year.
Cytosine was discovered and named by [[Albrecht Kossel]] and Albert Neumann in 1894 when it was hydrolyzed from calf [[thymus]] tissues.<ref>A. Kossel and Albert Neumann (1894) [http://gallica.bnf.fr/ark:/12148/bpt6k90735d/f437.image.langEN "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".)</ref><ref>{{cite journal |author1=Kossel, A. |author2=Steudel, H. Z. | journal = Physiol. Chem. | year = 1903 | volume = 38 |issue=1–2 | pages = 49–59 | doi = 10.1515/bchm2.1903.38.1-2.49 | title = Weitere Untersuchungen über das Cytosin|url=https://zenodo.org/record/1448762 }}</ref> A structure was proposed in 1903, and was synthesized (and thus confirmed) in the laboratory in the same year.


In 1997 cytosine was used in an early demonstration [[quantum information processing]] when Oxford University researchers implemented the [[Deutsch-Jozsa algorithm]] on a two [[qubit]] [[Nuclear magnetic resonance quantum computer#Overview of Liquid State Nuclear Magnetic Resonance Quantum Information Processing|nuclear magnetic resonance quantum computer (NMRQC)]].<ref>{{cite journal | last = Jones | first = J.A. | author2 = M. Mosca | title = Implementation of a quantum algorithm on a nuclear magnetic resonance quantum computer | journal = J. Chem. Phys. | volume = 109 | issue = 5 | pages = 1648–1653 | date = 1998-08-01 | url = http://www.citebase.org/abstract?id=oai%3AarXiv.org%3Aquant-ph%2F9801027 | doi = 10.1063/1.476739 | id = | accessdate = 2007-10-18 | arxiv = quant-ph/9801027 | archive-url = https://web.archive.org/web/20080612133706/http://www.citebase.org/abstract?id=oai%3AarXiv.org%3Aquant-ph%2F9801027 | archive-date = 2008-06-12 | dead-url = yes }}</ref>
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#Overview of Liquid State Nuclear Magnetic Resonance Quantum Information Processing|nuclear magnetic resonance quantum computer (NMRQC)]].<ref>{{cite journal | last = Jones | first = J.A. | author2 = M. Mosca | title = Implementation of a quantum algorithm on a nuclear magnetic resonance quantum computer | journal = J. Chem. Phys. | volume = 109 | issue = 5 | pages = 1648–1653 | date = 1998-08-01 | url = http://www.citebase.org/abstract?id=oai%3AarXiv.org%3Aquant-ph%2F9801027 | doi = 10.1063/1.476739 | access-date = 2007-10-18 | arxiv = quant-ph/9801027 | bibcode = 1998JChPh.109.1648J | s2cid = 19348964 | archive-url = https://web.archive.org/web/20080612133706/http://www.citebase.org/abstract?id=oai%3AarXiv.org%3Aquant-ph%2F9801027 | archive-date = 2008-06-12 | url-status = dead }}</ref>


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.<ref name="NASA-20150303">{{cite web |last=Marlaire |first=Ruth |title=NASA Ames Reproduces the Building Blocks of Life in Laboratory |url=http://www.nasa.gov/content/nasa-ames-reproduces-the-building-blocks-of-life-in-laboratory |date=3 March 2015 |work=[[NASA]] |accessdate=5 March 2015 }}</ref>
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.<ref name="NASA-20150303">{{cite web |last=Marlaire |first=Ruth |title=NASA Ames Reproduces the Building Blocks of Life in Laboratory |url=http://www.nasa.gov/content/nasa-ames-reproduces-the-building-blocks-of-life-in-laboratory |date=3 March 2015 |work=[[NASA]] |access-date=5 March 2015 |archive-date=5 March 2015 |archive-url=https://web.archive.org/web/20150305083306/http://www.nasa.gov/content/nasa-ames-reproduces-the-building-blocks-of-life-in-laboratory/ |url-status=dead }}</ref>


==Chemical reactions==
==Chemical reactions==
{{multiple image
[[File:Cytosine chemical structure.svg|thumb|left|100px|Cytosine with numbered components. [[Methylation]] occurs on carbon number 5.]]
| align=left
| total_width = 360
| image1=Cytonum2.svg
| caption1=Cytosine
| image2=Guannum2.svg
| caption2=[[Guanine]]
| footer=Cytosine and guanine with the direction of hydrogen bonding indicated (arrow points positive to negative charge).<br>[[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).
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]] ([[deamination|spontaneous deamination]]). This can lead to a [[point mutation]] if not repaired by the [[DNA repair]] [[enzyme]]s such as uracil glycosylase, which cleaves a uracil in DNA.
In DNA and RNA, cytosine is paired with [[guanine]]. However, it is inherently unstable, and can change into [[uracil]] ([[deamination|spontaneous deamination]]). This can lead to a [[point mutation]] if not repaired by the [[DNA repair]] [[enzyme]]s such as uracil glycosylase, which cleaves a uracil in DNA.


⚫
Cytosine can also be [[Methylation|methylated]] into [[5-Methylcytosine|5-methylcytosine]] by an enzyme called [[DNA methyltransferase]] or be methylated and [[Hydroxylation|hydroxylated]] to make [[5-Hydroxymethylcytosine|5-hydroxymethylcytosine]]. The difference in rates of deamination of cytosine and 5-methylcytosine (to uracil and [[thymine]]) forms the basis of [[bisulfite sequencing]].<ref>{{Cite journal|last=Hayatsu|first=Hikoya|date=2008|title=Discovery of bisulfite-mediated cytosine conversion to uracil, the key reaction for DNA methylation analysis — A personal account|journal=Proceedings of the Japan Academy. Series B, Physical and Biological Sciences|volume=84|issue=8|pages=321–330|doi=10.2183/pjab.84.321|issn=0386-2208|pmc=3722019|pmid=18941305|bibcode=2008PJAB...84..321H}}</ref>
{{clear}}

==Biological function==
When found third in a [[codon]] of [[RNA]], cytosine is synonymous with [[uracil]], as they are interchangeable as the third base.
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.
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.

⚫
Cytosine can also be [[Methylation|methylated]] into [[5-Methylcytosine|5-methylcytosine]] by an enzyme called [[DNA methyltransferase]] or be methylated and [[Hydroxylation|hydroxylated]] to make [[5-Hydroxymethylcytosine|5-hydroxymethylcytosine]]. The difference in rates of deamination of cytosine and 5-methylcytosine (to uracil and [[thymine]]) forms the basis of [[bisulfite sequencing]].<ref>{{Cite journal|last=Hayatsu|first=Hikoya|date=2008|title=Discovery of bisulfite-mediated cytosine conversion to uracil, the key reaction for DNA methylation analysis — A personal account|url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722019/|journal=Proceedings of the Japan Academy. Series B, Physical and Biological Sciences|volume=84|issue=8|pages=321–330|doi=10.2183/pjab/84.321|issn=0386-2208|pmc=3722019|pmid=18941305}}</ref>


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.<ref name="Chahwan">{{cite journal|author1=Chahwan R. |author2=Wontakal S.N. |author3=Roa S. | title=Crosstalk between genetic and epigenetic information through cytosine deamination| journal=Trends in Genetics| volume = 26| pages = 443–448| year = 2010 | doi = 10.1016/j.tig.2010.07.005| pmid = 20800313| issue = 10}}</ref> The implications of deamination on 5-hydroxymethylcytosine, on the other hand, remains less understood.
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.<ref name="Chahwan">{{cite journal|author1=Chahwan R. |author2=Wontakal S.N. |author3=Roa S. | title=Crosstalk between genetic and epigenetic information through cytosine deamination| journal=Trends in Genetics| volume = 26| pages = 443–448| year = 2010 | doi = 10.1016/j.tig.2010.07.005| pmid = 20800313| issue = 10}}</ref> The implications of deamination on 5-hydroxymethylcytosine, on the other hand, remains less understood.


== Theoretical aspects ==
== Theoretical aspects ==
Cytosine has not been found in meteorites, which suggests 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]].<ref>{{Cite news|url=https://blogs.scientificamerican.com/guest-blog/did-the-seeds-of-life-come-from-space/|title=Did the Seeds of Life Come from Space?|last=Tasker|first=Elizabeth|newspaper=Scientific American Blog Network|access-date=2016-11-24}}</ref>
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]].<ref>{{Cite news|url=https://blogs.scientificamerican.com/guest-blog/did-the-seeds-of-life-come-from-space/|title=Did the Seeds of Life Come from Space?|last=Tasker|first=Elizabeth|newspaper=Scientific American Blog Network|access-date=2016-11-24}}</ref>

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.<ref>{{cite web |author1=Yasuhiro Oba |author2=Yoshinori Takano |author3=Yoshihiro Furukawa |author4=Toshiki Koga |author5=Daniel P. Glavin |author6=Jason P. Dworkin |author7=Hiroshi Naraoka |title=Identifying the wide diversity of extraterrestrial purine and pyrimidine nucleobases in carbonaceous meteorites |url=https://www.nature.com/articles/s41467-022-29612-x#article-info |website=The Journal of Nature Communications |publisher=Nature.com |access-date=7 July 2022}}</ref>


==References==
==References==
Line 84: Line 96:
==External links and citations==
==External links and citations==
{{Commons category|Cytosine}}
{{Commons category|Cytosine}}
* [http://gmd.mpimp-golm.mpg.de/Spectrums/04ef65b4-ae00-4bbf-b115-64d1aa7e0fcd.aspx Cytosine MS Spectrum]
* [https://web.archive.org/web/20190416021636/http://gmd.mpimp-golm.mpg.de/Spectrums/04ef65b4-ae00-4bbf-b115-64d1aa7e0fcd.aspx Cytosine MS Spectrum]
*{{EINECSLink|200-749-5}}
*{{EINECSLink|200-749-5}}
* {{cite journal |author=Shapiro R |title=Prebiotic cytosine synthesis: a critical analysis and implications for the origin of life |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=96 |issue=8 |pages=4396–401 |year=1999 |pmid=10200273 |doi= 10.1073/pnas.96.8.4396|pmc=16343 }}
* {{cite journal |author=Shapiro R |title=Prebiotic cytosine synthesis: a critical analysis and implications for the origin of life |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=96 |issue=8 |pages=4396–401 |year=1999 |pmid=10200273 |doi= 10.1073/pnas.96.8.4396|pmc=16343 |bibcode=1999PNAS...96.4396S |doi-access=free }}


{{Nucleobases, nucleosides, and nucleotides}}
{{Nucleobases, nucleosides, and nucleotides}}

Revision as of 11:04, 9 April 2024

Not to be confused with cytokine, cytidine, cysteine, cystine, or cytisine.
Cytosine
Names
Preferred IUPAC name
4-Aminopyrimidin-2(1H)-one
Other names
4-Amino-1H-pyrimidine-2-one
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.681 Edit this at Wikidata
KEGG
MeSH Cytosine
UNII
  • InChI=1S/C4H5N3O/c5-3-1-2-6-4(8)7-3/h1-2H,(H3,5,6,7,8) checkY
    Key: OPTASPLRGRRNAP-UHFFFAOYSA-N checkY
  • 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).
checkY verify (what is checkY☒N ?)

Cytosine (/ˈsaɪtəˌsiːn, -ˌziːn, -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.

History

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

Cytosine
Guanine
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

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

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

  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). "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.
  7. ^ 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.
  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

Wikimedia Commons has media related to Cytosine.
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