Type of enzymes
DNA is wrapped around histones to form nucleosomes . Nucleosomes are shown as "beads on a string " with the distinction between euchromatin and heterochromatin .
The basic units of chromatin structure.
Histone-modifying enzymes are enzymes involved in the modification of histone substrates after protein translation and affect cellular processes including gene expression .[ 1] [ 2] To safely store the eukaryotic genome , DNA is wrapped around four core histone proteins (H3, H4, H2A, H2B), which then join to form nucleosomes . These nucleosomes further fold together into highly condensed chromatin , which renders the organism's genetic material far less accessible to the factors required for gene transcription , DNA replication , recombination and repair .[ 3] [ 4] Subsequently, eukaryotic organisms have developed intricate mechanisms to overcome this repressive barrier imposed by the chromatin through histone modification , a type of post-translational modification which typically involves covalently attaching certain groups to histone residues. Once added to the histone, these groups (directly or indirectly) elicit either a loose and open histone conformation, euchromatin , or a tight and closed histone conformation, heterochromatin . Euchromatin marks active transcription and gene expression , as the light packing of histones in this way allows entry for proteins involved in the transcription process. As such, the tightly packed heterochromatin marks the absence of current gene expression.[ 4]
While there exist several distinct post-translational modifications for histones , the four most common histone modifications include acetylation ,[ 5] methylation ,[ 6] phosphorylation [ 7] and ubiquitination .[ 8] Histone-modifying enzymes that induce a modification (e.g., add a functional group ) are dubbed writers, while enzymes that revert modifications are dubbed erasers. Furthermore, there are many uncommon histone modifications including O -GlcNAcylation ,[ 9] sumoylation ,[ 10] ADP-ribosylation ,[ 11] citrullination [ 12] [ 13] [ 14] and proline isomerization .[ 15] For a detailed example of histone modifications in transcription regulation see RNA polymerase control by chromatin structure and table "Examples of histone modifications in transcriptional regulation ".
^ Morgan MA, Shilatifard A (December 2020). "Reevaluating the roles of histone-modifying enzymes and their associated chromatin modifications in transcriptional regulation" . Nature Genetics . 52 (12): 1271–1281. doi :10.1038/s41588-020-00736-4 . PMID 33257899 . S2CID 227242638 .
^ Vinayachandran, V; et al. (14 February 2018). "Widespread and precise reprogramming of yeast protein-genome interactions in response to heat shock" . Genome Research . 28 (3): 357–366. doi :10.1101/gr.226761.117 . PMC 5848614 . PMID 29444801 .
^ McGinty RK, Tan S (March 2015). "Nucleosome structure and function" . Chemical Reviews . 115 (6): 2255–2273. doi :10.1021/cr500373h . PMC 4378457 . PMID 25495456 .
^ a b Kouzarides T (February 2007). "Chromatin modifications and their function" . Cell . 128 (4): 693–705. doi :10.1016/j.cell.2007.02.005 . PMID 17320507 . S2CID 11691263 .
^ Sterner DE, Berger SL (June 2000). "Acetylation of histones and transcription-related factors" . Microbiology and Molecular Biology Reviews . 64 (2): 435–459. doi :10.1128/MMBR.64.2.435-459.2000 . PMC 98999 . PMID 10839822 .
^ Zhang Y, Reinberg D (September 2001). "Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails" . Genes & Development . 15 (18): 2343–2360. doi :10.1101/gad.927301 . PMID 11562345 .
^ Nowak SJ, Corces VG (April 2004). "Phosphorylation of histone H3: a balancing act between chromosome condensation and transcriptional activation" . Trends in Genetics . 20 (4): 214–220. doi :10.1016/j.tig.2004.02.007 . PMID 15041176 .
^ Shilatifard A (2006). "Chromatin modifications by methylation and ubiquitination: implications in the regulation of gene expression" . Annual Review of Biochemistry . 75 : 243–269. doi :10.1146/annurev.biochem.75.103004.142422 . PMID 16756492 .
^ Sakabe K, Wang Z, Hart GW (November 2010). "Beta-N-acetylglucosamine (O-GlcNAc) is part of the histone code" . Proceedings of the National Academy of Sciences of the United States of America . 107 (46): 19915–19920. Bibcode :2010PNAS..10719915S . doi :10.1073/pnas.1009023107 . PMC 2993388 . PMID 21045127 .
^ Nathan D, Ingvarsdottir K, Sterner DE, Bylebyl GR, Dokmanovic M, Dorsey JA, et al. (April 2006). "Histone sumoylation is a negative regulator in Saccharomyces cerevisiae and shows dynamic interplay with positive-acting histone modifications" . Genes & Development . 20 (8): 966–976. doi :10.1101/gad.1404206 . PMC 1472304 . PMID 16598039 .
^ Hassa PO, Haenni SS, Elser M, Hottiger MO (September 2006). "Nuclear ADP-ribosylation reactions in mammalian cells: where are we today and where are we going?" . Microbiology and Molecular Biology Reviews . 70 (3): 789–829. doi :10.1128/MMBR.00040-05 . PMC 1594587 . PMID 16959969 .
^ Cuthbert GL, Daujat S, Snowden AW, Erdjument-Bromage H, Hagiwara T, Yamada M, et al. (September 2004). "Histone deimination antagonizes arginine methylation" . Cell . 118 (5): 545–553. doi :10.1016/j.cell.2004.08.020 . PMID 15339660 . S2CID 8948511 .
^ Wang Y, Wysocka J, Sayegh J, Lee YH, Perlin JR, Leonelli L, et al. (October 2004). "Human PAD4 regulates histone arginine methylation levels via demethylimination" . Science . 306 (5694): 279–283. Bibcode :2004Sci...306..279W . doi :10.1126/science.1101400 . PMID 15345777 . S2CID 1579362 .
^ Sams, K.L; Mukai, C; Marks, B.A; Mittal, C; Demeter, E.A; Nelissen, S; Grenier, J.K; Tate, A.E; Ahmed, F; Coonrod, S.A (October 2022). "Delayed puberty, gonadotropin abnormalities and subfertility in male Padi2/Padi4 double knockout mice" . Reprod Biol Endocrinol . 20 (1): 150. doi :10.1186/s12958-022-01018-w . PMC 9555066 . PMID 36224627 .
^ Nelson CJ, Santos-Rosa H, Kouzarides T (September 2006). "Proline isomerization of histone H3 regulates lysine methylation and gene expression" . Cell . 126 (5): 905–916. doi :10.1016/j.cell.2006.07.026 . PMID 16959570 . S2CID 17789997 .