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Gene Symbol |
HMGB2 |
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Aliases |
HMG2 |
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Entrez Gene ID |
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Gene Name |
High mobility group box 2 |
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Chromosomal Location |
4q34.1 |
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HGNC ID |
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Summary |
This gene encodes a member of the non-histone chromosomal high mobility group protein family. 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. [provided by RefSeq, Jul 2008]
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e!Ensembl
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Gene Ontology (GO)
GO ID |
Ontology |
Function |
Evidence |
Reference |
GO:0001938 |
Biological process |
Positive regulation of endothelial cell proliferation |
IDA |
19811285 |
GO:0006310 |
Biological process |
DNA recombination |
IBA |
21873635 |
GO:0006325 |
Biological process |
Chromatin organization |
NAS |
11909973 |
GO:0006334 |
Biological process |
Nucleosome assembly |
NAS |
11909973 |
GO:0006338 |
Biological process |
Chromatin remodeling |
IBA |
21873635 |
GO:0006357 |
Biological process |
Regulation of transcription by RNA polymerase II |
IBA |
21873635 |
GO:0006357 |
Biological process |
Regulation of transcription by RNA polymerase II |
IDA |
7797075 |
GO:0032075 |
Biological process |
Positive regulation of nuclease activity |
IDA |
978439 |
GO:0043388 |
Biological process |
Positive regulation of DNA binding |
IDA |
19965638 |
GO:0045089 |
Biological process |
Positive regulation of innate immune response |
IBA |
21873635 |
GO:0045648 |
Biological process |
Positive regulation of erythrocyte differentiation |
IMP |
19965638 |
GO:0045654 |
Biological process |
Positive regulation of megakaryocyte differentiation |
IMP |
19965638 |
GO:0045892 |
Biological process |
Negative regulation of transcription, DNA-templated |
IDA |
9636147 |
GO:0045893 |
Biological process |
Positive regulation of transcription, DNA-templated |
IDA |
19965638 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IBA |
21873635 |
GO:0045944 |
Biological process |
Positive regulation of transcription by RNA polymerase II |
IDA |
19223331, 19965638 |
GO:0050829 |
Biological process |
Defense response to Gram-negative bacterium |
IDA |
23877675 |
GO:0050830 |
Biological process |
Defense response to Gram-positive bacterium |
IDA |
23877675 |
GO:0060326 |
Biological process |
Cell chemotaxis |
IDA |
19811285 |
GO:0071222 |
Biological process |
Cellular response to lipopolysaccharide |
IEP |
19811285 |
GO:0000790 |
Cellular component |
Nuclear chromatin |
IBA |
21873635 |
GO:0000793 |
Cellular component |
Condensed chromosome |
IDA |
12925773 |
GO:0005615 |
Cellular component |
Extracellular space |
IDA |
19811285 |
GO:0005623 |
Cellular component |
Cell |
IDA |
15496585 |
GO:0005634 |
Cellular component |
Nucleus |
IDA |
8339930, 11909973 |
GO:0005737 |
Cellular component |
Cytoplasm |
IBA |
21873635 |
GO:0005737 |
Cellular component |
Cytoplasm |
IDA |
11909973 |
GO:0032991 |
Cellular component |
Protein-containing complex |
IDA |
11909973 |
GO:0048471 |
Cellular component |
Perinuclear region of cytoplasm |
IDA |
9010268, 11909973 |
GO:0003677 |
Molecular function |
DNA binding |
IMP |
11909973 |
GO:0003684 |
Molecular function |
Damaged DNA binding |
IDA |
8226934 |
GO:0003713 |
Molecular function |
Transcription coactivator activity |
IDA |
19223331 |
GO:0003723 |
Molecular function |
RNA binding |
HDA |
22658674, 22681889 |
GO:0005515 |
Molecular function |
Protein binding |
IPI |
9636147, 11909973, 25416956 |
GO:0008134 |
Molecular function |
Transcription factor binding |
IBA |
21873635 |
GO:0008301 |
Molecular function |
DNA binding, bending |
IBA |
21873635 |
GO:0008301 |
Molecular function |
DNA binding, bending |
IDA |
8339930, 11909973 |
GO:0042056 |
Molecular function |
Chemoattractant activity |
IDA |
19811285 |
GO:0044212 |
Molecular function |
Transcription regulatory region DNA binding |
IDA |
19965638 |
GO:0050786 |
Molecular function |
RAGE receptor binding |
IGI |
19811285 |
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Protein Information |
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Protein Name |
High mobility group protein B2, HMG-2, high mobility group protein 2, high-mobility group (nonhistone chromosomal) protein 2 |
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Function |
Multifunctional protein with various roles in different cellular compartments. May act in a redox sensitive manner. In the nucleus is an abundant chromatin-associated non-histone protein involved in transcription, chromatin remodeling and V(D)J recombination and probably other processes. Binds DNA with a preference to non-canonical DNA structures such as single-stranded DNA. Can bent DNA and enhance DNA flexibility by looping thus providing a mechanism to promote activities on various gene promoters by enhancing transcription factor binding and/or bringing distant regulatory sequences into close proximity (PubMed:7797075, PubMed:11909973, PubMed:19522541, PubMed:18413230, PubMed:19965638, PubMed:20123072). Involved in V(D)J recombination by acting as a cofactor of the RAG complex: acts by stimulating cleavage and RAG protein binding at the 23 bp spacer of conserved recombination signal sequences (RSS) (By similarity). Proposed to be involved in the innate immune response to nucleic acids by acting as a promiscuous immunogenic DNA/RNA sensor which cooperates with subsequent discriminative sensing by specific pattern recognition receptors (By similarity). In the extracellular compartment acts as a chemokine. Promotes proliferation and migration of endothelial cells implicating AGER/RAGE (PubMed:19811285). Has antimicrobial activity in gastrointestinal epithelial tissues (PubMed:23877675). Involved in inflammatory response to antigenic stimulus coupled with proinflammatory activity (By similarity). Involved in modulation of neurogenesis probably by regulation of neural stem proliferation (By similarity). Involved in articular cartilage surface maintenance implicating LEF1 and the Wnt/beta-catenin pathway (By similarity). |
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UniProt |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000276198 |
P28335 |
P28335 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Endocrine System Diseases |
PCOS |
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Neoplasms |
Liver Cancer |
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Lung Cancer |
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Nutritional and Metabolic Diseases |
Obesity |
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References |
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Xu Huiyu, Han Yong, Lou Jiaying, Zhang Hongxian, Zhao Yue, Gyorffy Balazs, Li Rong |
Department of Obstetrics and Gynecology, Reproductive Medical Center, Peking University Third Hospital, Beijing, P.R. China.| Department of Pathology, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang Province, P.R. China.| Department of Clinical Laboratory, Renmin Hospital of Xiaoshan District, Hangzhou, Zhejiang Province, P.R. China.| Department of Urology, Peking University Third Hospital, Beijing, P.R. China.| Department of Obstetrics and Gynecology, Reproductive Medical Center, Peking University Third Hospital, Beijing, P.R. China.| Momentum Cancer Biomarker Research Group, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.| Second Department of Pediatrics, Semmelweis University, Budapest, Hungary.| Department of Obstetrics and Gynecology, Reproductive Medical Center, Peking University Third Hospital, Beijing, P.R. China. |
Oncotarget. 2017 May 13;8(41):69520-69526. doi: 10.18632/oncotarget.17846. |
Abstract
To explore the key genes associated with both PCOS and breast cancer, we overlapped the synchronously differently expressed genes in two obese insulin-resistant GEO datasets in muscle tissue and genes exert essential roles in breast cancer prognosis together base on the following reasons: (1) Androgens excess is believed to contribute to the onset of both PCOS and breast cancer. (2) PCOS is usually complicated with metabolic symptoms, such as obesity and insulin-resistance. (3) Muscle is the main place where energy metabolism and material metabolism take place. Consequently, 53 genes were found, functionally enriched in pathways such as pyruvate metabolism, muscle system process and development of primary male sexual characteristics etc. We further lay our eyes on genes correlated with male sexual characteristics, which may be involved in the onset of both PCOS and breast cancer. Three genes were indicated to be associated with this process, including hydroxysteroid (17-beta) dehydrogenase 4/HSD17B4, platelet-derived growth factor receptor, alpha polypeptide/PDGFRA and high-mobility group box 2/HMGB2. Gene-drug interaction network about the three genes were then constructed. Drugs or chemicals that contribute to correcting the disorder of lipid metabolism were detected to restore the abnormal expression of the three genes in PCOS, such as simvastatin, bezafibrate, fenofibrate et al, which provide further choices for managing patients with PCOS. |
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