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  2. Thymine - Wikipedia

    en.wikipedia.org/wiki/Thymine

    As its alternate name (5-methyluracil) suggests, thymine may be derived by methylation of uracil at the 5th carbon. In RNA, thymine is replaced with uracil in most cases. In DNA, thymine (T) binds to adenine (A) via two hydrogen bonds, thereby stabilizing the nucleic acid structures. Thymine combined with deoxyribose creates the nucleoside ...

  3. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    The purine nitrogenous bases are characterized by their single amino group (−NH 2), at the C6 carbon in adenine and C2 in guanine. [5] Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases. [6]

  4. 5-Methylcytosine - Wikipedia

    en.wikipedia.org/wiki/5-Methylcytosine

    5-Methylcytosine is a methylated form of the DNA base cytosine (C) that regulates gene transcription and takes several other biological roles. [1] When cytosine is methylated, the DNA maintains the same sequence, but the expression of methylated genes can be altered (the study of this is part of the field of epigenetics). 5-Methylcytosine is incorporated in the nucleoside 5-methylcytidine.

  5. DNA methylation - Wikipedia

    en.wikipedia.org/wiki/DNA_methylation

    Methylation of cytosine to form 5-methylcytosine occurs at the same 5 position on the pyrimidine ring where the DNA base thymine's methyl group is located; the same position distinguishes thymine from the analogous RNA base uracil, which has no methyl group. Spontaneous deamination of 5-methylcytosine converts it to thymine. This results in a T ...

  6. 5,6-Dihydro-5 (α-thyminyl)thymine - Wikipedia

    en.wikipedia.org/wiki/5,6-Dihydro-5(α-thyminyl...

    5,6-Dihydro-5(α-thyminyl)thymine is a DNA pyrimidine dimer photoproduct produced when DNA in bacterial spores is exposed to ultraviolet light. [1] In bacteria, this DNA base dimer deforms the structure of DNA, so endospore forming bacteria have an enzyme called spore photoproduct lyase that repairs this damage.

  7. Bisulfite sequencing - Wikipedia

    en.wikipedia.org/wiki/Bisulfite_sequencing

    In oxidative bisulfite sequencing (oxBS), Tet is used to convert 5-hydroxymethylcytosine to 5-formylcytosine, which subsequently converts to uracil during bisulfite treatment. [35] The only base that then reads as a C is 5‑methylcytosine, giving a map of the true methylation status in the DNA sample.

  8. Uracil - Wikipedia

    en.wikipedia.org/wiki/Uracil

    In DNA, the uracil nucleobase is replaced by thymine (T). Uracil is a demethylated form of thymine. Uracil is a common and naturally occurring pyrimidine derivative. [2] The name "uracil" was coined in 1885 by the German chemist Robert Behrend, who was attempting to synthesize derivatives of uric acid. [3]

  9. Cytosine - Wikipedia

    en.wikipedia.org/wiki/Cytosine

    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]