This gene encodes a member of the non-histone chromosomal high-mobility group protein family.[3] The proteins of this family are chromatin-associated and ubiquitously distributed in the nucleus of higher eukaryotic cells. In vitro studies have demonstrated that this protein is able to efficiently bend DNA and form DNA circles. These studies suggest a role in facilitating cooperative interactions between cis-acting proteins by promoting DNA flexibility. This protein was also reported to be involved in the final ligation step in DNA end-joining processes of DNA double-strand breaks repair and V(D)J recombination.[2]
↑Murugesapillai D, McCauley MJ, Maher LJ, Williams MC (15 November 2016). "Single-molecule studies of high-mobility group B architectural DNA bending proteins". Biophysical Reviews. doi:10.1007/s12551-016-0236-4.
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Shykind BM, Kim J, Sharp PA (Jun 1995). "Activation of the TFIID-TFIIA complex with HMG-2". Genes & Development. 9 (11): 1354–65. doi:10.1101/gad.9.11.1354. PMID7797075.
Paull TT, Haykinson MJ, Johnson RC (Aug 1993). "The nonspecific DNA-binding and -bending proteins HMG1 and HMG2 promote the assembly of complex nucleoprotein structures". Genes & Development. 7 (8): 1521–34. doi:10.1101/gad.7.8.1521. PMID8339930.
Wanschura S, Schoenmakers EF, Huysmans C, Bartnitzke S, Van de Ven WJ, Bullrdiek J (Jan 1996). "Mapping of the human HMG2 gene to 4q31". Genomics. 31 (2): 264–5. doi:10.1006/geno.1996.0046. PMID8824816.
Nagaki S, Yamamoto M, Yumoto Y, Shirakawa H, Yoshida M, Teraoka H (May 1998). "Non-histone chromosomal proteins HMG1 and 2 enhance ligation reaction of DNA double-strand breaks". Biochemical and Biophysical Research Communications. 246 (1): 137–41. doi:10.1006/bbrc.1998.8589. PMID9600082.
Yumoto Y, Shirakawa H, Yoshida M, Suwa A, Watanabe F, Teraoka H (Sep 1998). "High mobility group proteins 1 and 2 can function as DNA-binding regulatory components for DNA-dependent protein kinase in vitro". Journal of Biochemistry. 124 (3): 519–27. doi:10.1093/oxfordjournals.jbchem.a022143. PMID9722660.
Butteroni C, De Felici M, Schöler HR, Pesce M (Dec 2000). "Phage display screening reveals an association between germline-specific transcription factor Oct-4 and multiple cellular proteins". Journal of Molecular Biology. 304 (4): 529–40. doi:10.1006/jmbi.2000.4238. PMID11099378.
Stros M, Ozaki T, Bacikova A, Kageyama H, Nakagawara A (Mar 2002). "HMGB1 and HMGB2 cell-specifically down-regulate the p53- and p73-dependent sequence-specific transactivation from the human Bax gene promoter". The Journal of Biological Chemistry. 277 (9): 7157–64. doi:10.1074/jbc.M110233200. PMID11748232.
Dubois T, Howell S, Zemlickova E, Aitken A (Apr 2002). "Identification of casein kinase Ialpha interacting protein partners". FEBS Letters. 517 (1–3): 167–71. doi:10.1016/S0014-5793(02)02614-5. PMID12062430.
Fan Z, Beresford PJ, Zhang D, Xu Z, Novina CD, Yoshida A, Pommier Y, Lieberman J (Feb 2003). "Cleaving the oxidative repair protein Ape1 enhances cell death mediated by granzyme A". Nature Immunology. 4 (2): 145–53. doi:10.1038/ni885. PMID12524539.
Lv X, Xu DD, Liu DP, Li L, Hao DL, Liang CC (2003). "High-mobility group protein 2 may be involved in the locus control region regulation of the beta-globin gene cluster". Biochemistry and Cell Biology. 80 (6): 765–70. doi:10.1139/o02-164. PMID12555809.
Aird KM, Iwasaki O, Kossenkov AV, Tanizawa H, Fatkhutdinov N, Bitler BG, Le L, Alicea G, Yang TL, Johnson FB, Noma K, Zhang R (Oct 2016). "HMGB2 orchestrates the chromatin landscape of senescence-associated secretory phenotype gene loci"(PDF). JCB. doi:10.1083/jcb.201608026. Loss of HMGB2 (High-mobility group protein box 2) during senescence blunts SASP (senescence-associated secretory phenotype) gene expression by allowing for spreading of repressive heterochromatin into SASP gene loci. This correlates with incorporation of SASP gene loci into SAHF (senescence-associated heterochromatin foci), which in turn represses SASP gene expression