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Histone H4

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H4 histone, family 3
Identifiers
SymbolH4F3
NCBI gene3023
HGNC4780
UniProtP62805
Other data
LocusChr. 3 q13.13
Search for
StructuresSwiss-model
DomainsInterPro
Basic units of chromatin structure

Histone H4 is one of the five main histone proteins involved in the structure of chromatin in eukaryotic cells. Featuring a main globular domain and a long N-terminal tail, H4 is involved with the structure of the nucleosome of the 'beads on a string' organization. Histone proteins are highly post-translationally modified. Covalently bonded modifications include acetylation and methylation of the N-terminal tails. These modifications may alter expression of genes located on DNA associated with its parent histone octamer.[1][2] Histone H4 is an important protein in the structure and function of chromatin, where its sequence variants and variable modification states are thought to play a role in the dynamic and long term regulation of genes.

Genetics

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Histone H4 is encoded in multiple genes at different loci including: HIST1H4A, HIST1H4B, HIST1H4C, HIST1H4D, HIST1H4E, HIST1H4F, HIST1H4G, HIST1H4H, HIST1H4I, HIST1H4J, HIST1H4K, HIST1H4L, HIST2H4A, HIST2H4B, HIST4H4.

Evolution

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Histone proteins are among the most highly conserved eukaryotic proteins. For example, the amino acid sequence of histone H4 from a pea and cow differ at only 2 out of the 102 positions. This evolutionary conservation suggests that the functions of histone proteins involve nearly all of their amino acids so that any change is deleterious to the cell. Most changes in histone sequences are lethal; the few that are not lethal cause changes in the pattern of gene expression as well as other abnormalities.[3]

Structure

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Histone H4 is a 102 to 135 amino acid protein which shares a structural motif, known as the histone fold, formed from three a-helices connected by two loops. Histone proteins H3 and H4 bind to form a H3-H4 dimer, two of these H3-H4 dimers combine to form a tetramer. This tetramer further combines with two H2a-H2b dimers to form the compact Histone octamer core.[3]

Sequence variants

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Histone H4 is one of the slowest evolving proteins. There are H4 genes that are constitutively expressed throughout the cell cycle that encode for proteins that are identical in sequence to the major H4.[4] Variants in human histone H4 were only recently discovered and are very rare.[5][6][7]

Pathogenic de novo missense variants have been identified in six H4 genes (HIST1H4C, HIST1H4D, HIST1H4E, HIST1H4F, HIST1H4I, HIST1H4J) in 33 individuals total, all presenting with neurodevelopmental features of intellectual disability and motor and/or gross developmental delay, but with variable non-neurological features. Ten amino acids were affected, six of which were found recurrently. These mutations were located within either the H4 core globular domain (involved in protein-protein interaction) or C-terminal tail (involved in post-translational modification).[5][6][7]

Alternative translation

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The Osteogenic Growth Peptide (OGP) is a 14-aa peptide produced from alternative translation of histone H4 mRNA, sharing the C-terminal sequence ALKRQGRTLYGFGG of histone H4. Translation is initiated at the 85th amino acid of the histone H4 mRNA, resulting in a 19-aa peptide (preOGP). This is converted into OGP through the cleavage of 5 amino-terminal residues.[8] It is found in human and rat circulation as well as regenerating bone marrow. In blood serum it is bound to α2M along with two other binding proteins that are not clearly identified. A specific receptor has not been identified, but some signaling pathways involved in its bone-regenaration function has been elucidated.[9]

Post-translational modifications

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Eukaryotic organisms can produce small amounts of specialized variant core histones that differ in amino acid sequence from the main ones. These variants with a variety of covalent modifications on the N-terminal can be added to histones making possible different chromatin structures that are required for DNA function in higher eukaryotes. Potential modifications include methylation (mono-, di-, or tri-methylation) or acetylation on the tails.[3]

Methylation

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Histone methylation occurs on arginine, lysine and histidine amino acids residues. Mono-, di- or tri-methylation has been discovered on histone H2A, H3 and H4.[10] Histone methylation has been associated with various cellular functions such as transcription, DNA replication, and DNA damage response including repair, heterochromatin formation, and somatic cell reprogramming. Among these biological functions, transcriptional repression and activation are the most studied.[10] Studies have shown that H4R3 methylation by PRMT1 (a histone methyltransferase) appears to be essential in vivo for the establishment or maintenance of a wide range of “active” chromatin modifications. Also methylation of histone H4 by PRMT1 was sufficient to permit subsequent acetylation on the N-terminal tail. However, acetylation of H4 inhibits its methylation by PRMT1.[11]

Acetylation

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Acetylation of histones is thought to relax condensed heterochromatin as the negative charge of acetyl groups can repel the DNA phosphate backbone charges, thus reducing the histone binding affinity for DNA. This hypothesis was validated by the discovery of the histone acetyltransferase (HAT) activity of several transcriptional activator complexes.[10] Histone acetylation influences chromatin structure in several ways. First, it can provide a tag for the binding of proteins that contain areas which recognize the acetylated tails. Secondly, it can block the function of chromatin remodelers.[12] Thirdly, it neutralizes the positive charge on lysines.[12] Acetylation of histone H4 on lysine 16 (H4K16ac) is especially important for chromatin structure and function in a variety of eukaryotes and is catalyzed by specific histone lysine acetyltransferases (HATs). H4K16 is particularly interesting because this is the only acetylatable site of the H4 N-terminal tail, and can influence the formation of a compact higher-order chromatin structure.[12] Hypoacetylation of H4K16 appears to cause delayed recruitment of DNA repair proteins to sites of DNA damage in a mouse model of the premature aging syndrome Hutchinson Gilford progeria.[13] H4K16Ac also has roles in transcriptional activation and the maintenance of euchromatin.[14] Additional acetylations include K31ac and K79ac.[15]

List of H4 modifications

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H4S1p

H4R3me2

H4K5ac

H4K8ac

H4K12ac

H4K16ac

H4K16adp

H4K20me

H4K31ac

H4S47o-p

H4K79ac

H4K91ac

H4K91ub[16]

See also

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References

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  1. ^ Bhasin M, Reinherz EL, Reche PA (2006). "Recognition and classification of histones using support vector machine" (PDF). Journal of Computational Biology. 13 (1): 102–112. doi:10.1089/cmb.2006.13.102. PMID 16472024.
  2. ^ Hartl DL, Freifelder D, Snyder LA (1988). Basic Genetics. Boston: Jones and Bartlett Publishers. ISBN 978-0-86720-090-4.
  3. ^ a b c Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2008). Molecular Biology of the Cell (5th ed.). Spring 2014. ISBN 978-0-8153-4105-5. OCLC 82473851.
  4. ^ Kamakaka RT, Biggins S (February 2005). "Histone variants: deviants?". Genes & Development. 19 (3): 295–310. doi:10.1101/gad.1272805. PMID 15687254.
  5. ^ a b Tessadori F, Giltay JC, Hurst JA, Massink MP, Duran K, Vos HR, et al. (November 2017). "Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control". Nature Genetics. 49 (11): 1642–1646. doi:10.1038/ng.3956. PMID 28920961. S2CID 23404727.
  6. ^ a b Tessadori F, Rehman AU, Giltay JC, Xia F, Streff H, Duran K, et al. (May 2020). "A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder". European Journal of Human Genetics. 28 (5): 674–678. doi:10.1038/s41431-019-0552-9. PMC 7171094. PMID 31804630.
  7. ^ a b Tessadori F, Duran K, Knapp K, Fellner M, Smithson S, Beleza Meireles A, et al. (April 2022). "Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome". American Journal of Human Genetics. 109 (4): 750–758. doi:10.1016/j.ajhg.2022.02.003. PMC 9069069. PMID 35202563.
  8. ^ Bab I, Smith E, Gavish H, Attar-Namdar M, Chorev M, Chen YC, et al. (May 1999). "Biosynthesis of osteogenic growth peptide via alternative translational initiation at AUG85 of histone H4 mRNA". The Journal of Biological Chemistry. 274 (20): 14474–14481. doi:10.1074/jbc.274.20.14474. PMID 10318873.
  9. ^ Pigossi SC, Medeiros MC, Saska S, Cirelli JA, Scarel-Caminaga RM (November 2016). "Role of Osteogenic Growth Peptide (OGP) and OGP(10-14) in Bone Regeneration: A Review". International Journal of Molecular Sciences. 17 (11): 1885. doi:10.3390/ijms17111885. PMC 5133884. PMID 27879684.
  10. ^ a b c Kim JK, Samaranayake M, Pradhan S (February 2009). "Epigenetic mechanisms in mammals". Cellular and Molecular Life Sciences. 66 (4): 596–612. doi:10.1007/s00018-008-8432-4. PMC 2780668. PMID 18985277.
  11. ^ Huang S, Litt M, Felsenfeld G (August 2005). "Methylation of histone H4 by arginine methyltransferase PRMT1 is essential in vivo for many subsequent histone modifications". Genes & Development. 19 (16): 1885–1893. doi:10.1101/gad.1333905. PMC 1186188. PMID 16103216.
  12. ^ a b c Taylor GC, Eskeland R, Hekimoglu-Balkan B, Pradeepa MM, Bickmore WA (December 2013). "H4K16 acetylation marks active genes and enhancers of embryonic stem cells, but does not alter chromatin compaction". Genome Research. 23 (12): 2053–2065. doi:10.1101/gr.155028.113. PMC 3847775. PMID 23990607.
  13. ^ Krishnan V, Chow MZ, Wang Z, Zhang L, Liu B, Liu X, et al. (July 2011). "Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice". Proceedings of the National Academy of Sciences of the United States of America. 108 (30): 12325–12330. Bibcode:2011PNAS..10812325K. doi:10.1073/pnas.1102789108. PMC 3145730. PMID 21746928.
  14. ^ Shogren-Knaak M, Ishii H, Sun JM, Pazin MJ, Davie JR, Peterson CL (February 2006). "Histone H4-K16 acetylation controls chromatin structure and protein interactions". Science. 311 (5762): 844–847. Bibcode:2006Sci...311..844S. doi:10.1126/science.1124000. PMID 16469925. S2CID 11079405.
  15. ^ Dang X, Scotcher J, Wu S, Chu RK, Tolić N, Ntai I, et al. (May 2014). "The first pilot project of the consortium for top-down proteomics: a status report". Proteomics. 14 (10): 1130–1140. doi:10.1002/pmic.201300438. PMC 4146406. PMID 24644084.
  16. ^ "Epigenetic modifications poster | Abcam". Retrieved 25 November 2019.

See also

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