H3K36me

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H3K36me is an

epigenetic modification to the DNA packaging protein Histone H3, specifically, the mono-methylation at the 36th lysine
residue of the histone H3 protein.

There are diverse modifications at H3K36, such as phosphorylation, methylation, acetylation, and ubiquitylation, which have many important biological processes.[1] The methylation of H3K36 has particularly had effects in transcriptional repression, alternative splicing, dosage compensation, DNA replication and repair, DNA methylation, and the transmission of the memory of gene expression from parents to offspring during development.[1]

Nomenclature

H3K36me2 indicates dimethylation of lysine 36 on histone H3 protein subunit:[2]

Abbr. Meaning
H3 H3 family of histones
K standard abbreviation for lysine
36 position of amino acid residue

(counting from N-terminus)

me methyl group
1 number of methyl groups added

Lysine methylation

Methylation-lysine

This diagram shows the progressive methylation of a lysine residue. The mono-methylation (second from left) denotes the methylation present in H3K36me1.

Lysine methylation is the addition of a methyl group to the lysine of histone proteins.[3] This occurs via histone lysine methyltransferase (HMTase) that utilize S-adenosylmethionine to specifically place the methyl group on histone Lys or Arg residues.[1] So far, there have only been eight specific mammalian enzymes discovered that can methylate H3K36 in vitro and/or in vivo, all of which have identical catalytic SET domains but, different preferences for Lys36 residues in different methylation states.[1]

Histone modifications

The genomic DNA of eukaryotic cells is wrapped around special protein molecules known as

histones. The complexes formed by the looping of the DNA are known as chromatin. The basic structural unit of chromatin is the nucleosome, which consists of the core octamer of histones (H2A, H2B, H3, and H4) as well as a linker histone and about 180 base pairs of DNA wrapped around it. These core histones are rich in lysine and arginine residues. The carboxyl (C) terminal end of these histones contribute to histone-histone interactions, as well as histone-DNA interactions. The amino (N) terminal charged tails are the site of the post-translational modifications, such as the one seen in H3K36me3.[4][5]

Epigenetic implications

The post-translational modification of histone tails by either histone-modifying complexes or chromatin remodeling complexes is interpreted by the cell and leads to the complex, combinatorial transcriptional output. It is thought that a

ChIP-sequencing revealed regions in the genome characterized by different banding.[8] Different developmental stages were profiled in Drosophila as well, an emphasis was placed on histone modification relevance.[9] A look into the data obtained led to the definition of chromatin states based on histone modifications.[10]
Certain modifications were mapped and enrichment was seen to localize in certain genomic regions. Five core histone modifications were found with each respective one being linked to various cell functions.

The human genome was annotated with chromatin states. These annotated states can be used as new ways to annotate a genome independently of the underlying genome sequence. This independence from the DNA sequence enforces the epigenetic nature of histone modifications. Chromatin states are also useful in identifying regulatory elements that have no defined sequence, such as enhancers. This additional level of annotation allows for a deeper understanding of cell-specific gene regulation.[11]

Methods

The histone mark H3K36me can be detected in a variety of ways:

  1. Chromatin
    ChIP-sequencing) measures the amount of DNA enrichment once bound to a targeted protein and immunoprecipitated. It results in good optimization and is used in vivo to reveal DNA-protein binding occurring in cells. ChIP-Seq can be used to identify and quantify various DNA fragments for different histone modifications along a genomic region.[12]
  2. Micrococcal Nuclease sequencing (MNase-seq) is used to investigate regions that are bound by well-positioned nucleosomes. The use of the micrococcal nuclease enzyme is employed to identify nucleosome positioning. Well-positioned nucleosomes are seen to have enrichment of sequences.[13]
  3. Assay for transposase accessible chromatin sequencing (ATAC-seq) is used to look into regions that are nucleosome-free (open chromatin). It uses hyperactive
    Tn5 transposon to highlight nucleosome localization.[14][15][16]

See also

References

  1. ^
    PMID 22266761
    .
  2. ISBN 978-0-12-799958-6
    .
  3. S2CID 140312035
    .
  4. PMID 18037899
    .
  5. PMID 17320507
    .
  6. S2CID 1883924
    .
  7. PMID 17571346
    .
  8. PMID 20888037
    .
  9. PMID 21177974
    .
  10. PMID 21179089
    .
  11. PMID 25693563
    .
  12. ^ "Whole-Genome Chromatin IP Sequencing (ChIP-Seq)"(PDF). Illumina. Retrieved 23 October 2019.
  13. ^ "MAINE-Seq/Mnase-Seq". illumina. Retrieved 23 October 2019.
  14. PMID 25559105
    .
  15. PMID 26314830
    .
  16. PMID 20150147
    .
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