SOCS2

Protein-coding gene in the species Homo sapiens
SOCS2
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2C9W, 4JGH, 5BO4

Identifiers
AliasesSOCS2, CIS2, Cish2, SOCS-2, SSI-2, SSI2, STATI2, suppressor of cytokine signaling 2
External IDsOMIM: 605117; MGI: 1201787; HomoloGene: 2880; GeneCards: SOCS2; OMA:SOCS2 - orthologs
Gene location (Human)
Chromosome 12 (human)
Chr.Chromosome 12 (human)[1]
Chromosome 12 (human)
Genomic location for SOCS2
Genomic location for SOCS2
Band12q22Start93,569,814 bp[1]
End93,583,487 bp[1]
Gene location (Mouse)
Chromosome 10 (mouse)
Chr.Chromosome 10 (mouse)[2]
Chromosome 10 (mouse)
Genomic location for SOCS2
Genomic location for SOCS2
Band10 C2|10 49.35 cMStart95,221,224 bp[2]
End95,253,042 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • secondary oocyte

  • canal of the cervix

  • vena cava

  • body of uterus

  • myometrium

  • seminal vesicula

  • Epithelium of choroid plexus

  • ectocervix

  • prostate

  • pituitary gland
Top expressed in
  • cumulus cell

  • Ileal epithelium

  • olfactory epithelium

  • vestibular membrane of cochlear duct

  • left lung lobe

  • vestibular sensory epithelium

  • stria vascularis

  • Gonadal ridge

  • right lung

  • interventricular septum
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
  • insulin-like growth factor receptor binding
  • protein kinase inhibitor activity
  • JAK pathway signal transduction adaptor activity
  • protein binding
  • growth hormone receptor binding
  • 1-phosphatidylinositol-3-kinase regulator activity
Cellular component
  • cytoplasm
  • cytosol
  • phosphatidylinositol 3-kinase complex
Biological process
  • receptor signaling pathway via JAK-STAT
  • response to estradiol
  • intracellular signal transduction
  • negative regulation of protein kinase activity
  • cytokine-mediated signaling pathway
  • negative regulation of apoptotic process
  • negative regulation of insulin receptor signaling pathway
  • cellular response to hormone stimulus
  • growth hormone receptor signaling pathway
  • regulation of signal transduction
  • regulation of cell growth
  • protein ubiquitination
  • regulation of growth
  • negative regulation of signal transduction
  • negative regulation of receptor signaling pathway via JAK-STAT
  • positive regulation of signal transduction
  • lactation
  • regulation of multicellular organism growth
  • negative regulation of multicellular organism growth
  • post-translational protein modification
  • positive regulation of neuron differentiation
  • mammary gland alveolus development
  • interleukin-7-mediated signaling pathway
  • regulation of phosphatidylinositol 3-kinase activity
  • phosphatidylinositol phosphate biosynthetic process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

8835

216233

Ensembl

ENSG00000120833

ENSMUSG00000020027

UniProt

O14508

O35717

RefSeq (mRNA)
NM_001270467
NM_001270468
NM_001270469
NM_001270470
NM_001270471

NM_003877

NM_001168655
NM_001168656
NM_001168657
NM_007706

RefSeq (protein)
NP_001257396
NP_001257397
NP_001257398
NP_001257399
NP_001257400

NP_003868

NP_001162126
NP_001162127
NP_001162128
NP_031732

Location (UCSC)Chr 12: 93.57 – 93.58 MbChr 10: 95.22 – 95.25 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Suppressor of cytokine signaling 2 is a protein that in humans is encoded by the SOCS2 gene.[5][6][7]

This gene encodes a member of the STAT-induced STAT inhibitor (SSI), also known as suppressor of cytokine signalling (SOCS), family. SSI family members are cytokine-inducible negative regulators of cytokine signaling. The expression of this gene can be induced by a subset of cytokines, including erythropoietin, GM-CSF, IL10 and interferon-gamma (IFN-gamma). The protein encoded by this gene is found to interact with the cytoplasmic domain of insulin-like growth factor 1 receptor (IGF1R), and thus is thought to be involved in the regulation of IGF1R mediated cell signaling.[8] Knockout studies in mice also suggested a regulatory role of this gene in IGF-1 related growth control.[7][9]

Interactions

SOCS2 has been shown to interact with insulin-like growth factor 1 receptor[8] and erythropoietin receptor.[10] Additionally, it acts as a substrate recognition subunit of a Cullin5 E3 ubiquitin ligase complex.[11] It is under investigation for use in targeted protein degradation.[12]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000120833 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020027 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Masuhara M, Sakamoto H, Matsumoto A, Suzuki R, Yasukawa H, Mitsui K, et al. (October 1997). "Cloning and characterization of novel CIS family genes". Biochemical and Biophysical Research Communications. 239 (2): 439–446. doi:10.1006/bbrc.1997.7484. PMID 9344848.
  6. ^ Minamoto S, Ikegame K, Ueno K, Narazaki M, Naka T, Yamamoto H, et al. (August 1997). "Cloning and functional analysis of new members of STAT induced STAT inhibitor (SSI) family: SSI-2 and SSI-3". Biochemical and Biophysical Research Communications. 237 (1): 79–83. doi:10.1006/bbrc.1997.7080. PMID 9266833.
  7. ^ a b "Entrez Gene: SOCS2 suppressor of cytokine signaling 2".
  8. ^ a b Dey BR, Spence SL, Nissley P, Furlanetto RW (September 1998). "Interaction of human suppressor of cytokine signaling (SOCS)-2 with the insulin-like growth factor-I receptor". The Journal of Biological Chemistry. 273 (37): 24095–24101. doi:10.1074/jbc.273.37.24095. PMID 9727029.
  9. ^ Greenhalgh CJ, Bertolino P, Asa SL, Metcalf D, Corbin JE, Adams TE, et al. (June 2002). "Growth enhancement in suppressor of cytokine signaling 2 (SOCS-2)-deficient mice is dependent on signal transducer and activator of transcription 5b (STAT5b)". Molecular Endocrinology. 16 (6): 1394–1406. doi:10.1210/mend.16.6.0845. PMID 12040024.
  10. ^ Eyckerman S, Verhee A, der Heyden JV, Lemmens I, Ostade XV, Vandekerckhove J, Tavernier J (December 2001). "Design and application of a cytokine-receptor-based interaction trap". Nature Cell Biology. 3 (12): 1114–1119. doi:10.1038/ncb1201-1114. PMID 11781573. S2CID 10228882.
  11. ^ Kung WW, Ramachandran S, Makukhin N, Bruno E, Ciulli A (June 2019). "Structural insights into substrate recognition by the SOCS2 E3 ubiquitin ligase". Nature Communications. 10 (1): 2534. Bibcode:2019NatCo..10.2534K. doi:10.1038/s41467-019-10190-4. PMC 6557900. PMID 31182716.
  12. ^ Ramachandran S, Makukhin N, Haubrich K, Nagala M, Forrester B, Lynch D, et al. (2022-10-18). "Structure-based design of a phosphotyrosine-masked covalent ligand targeting the E3 ligase SOCS2". Nature Communications. 14 (1): 6345. doi:10.1038/s41467-023-41894-3. PMC 10564737. PMID 37816714.

Further reading

  • Lopaczynski W (1999). "Differential regulation of signaling pathways for insulin and insulin-like growth factor I". Acta Biochimica Polonica. 46 (1): 51–60. doi:10.18388/abp.1999_4183. PMID 10453981.
  • Wang J, Campbell IL (February 2002). "Cytokine signaling in the brain: putting a SOCS in it?". Journal of Neuroscience Research. 67 (4): 423–427. doi:10.1002/jnr.10145. PMID 11835308. S2CID 33269663.
  • Kile BT, Schulman BA, Alexander WS, Nicola NA, Martin HM, Hilton DJ (May 2002). "The SOCS box: a tale of destruction and degradation". Trends in Biochemical Sciences. 27 (5): 235–241. doi:10.1016/S0968-0004(02)02085-6. PMID 12076535.
  • Pezet A, Buteau H, Kelly PA, Edery M (May 1997). "The last proline of Box 1 is essential for association with JAK2 and functional activation of the prolactin receptor". Molecular and Cellular Endocrinology. 129 (2): 199–208. doi:10.1016/S0303-7207(97)00063-4. PMID 9202403. S2CID 10606236.
  • Dey BR, Spence SL, Nissley P, Furlanetto RW (September 1998). "Interaction of human suppressor of cytokine signaling (SOCS)-2 with the insulin-like growth factor-I receptor". The Journal of Biological Chemistry. 273 (37): 24095–24101. doi:10.1074/jbc.273.37.24095. PMID 9727029.
  • Pezet A, Favre H, Kelly PA, Edery M (August 1999). "Inhibition and restoration of prolactin signal transduction by suppressors of cytokine signaling". The Journal of Biological Chemistry. 274 (35): 24497–24502. doi:10.1074/jbc.274.35.24497. PMID 10455112.
  • Yandava CN, Pillari A, Drazen JM (October 1999). "Radiation hybrid and cytogenetic mapping of SOCS1 and SOCS2 to chromosomes 16p13 and 12q, respectively". Genomics. 61 (1): 108–111. doi:10.1006/geno.1999.5937. PMID 10512686.
  • Ram PA, Waxman DJ (December 1999). "SOCS/CIS protein inhibition of growth hormone-stimulated STAT5 signaling by multiple mechanisms". The Journal of Biological Chemistry. 274 (50): 35553–35561. doi:10.1074/jbc.274.50.35553. PMID 10585430.
  • Metcalf D, Greenhalgh CJ, Viney E, Willson TA, Starr R, Nicola NA, et al. (June 2000). "Gigantism in mice lacking suppressor of cytokine signalling-2". Nature. 405 (6790): 1069–1073. Bibcode:2000Natur.405.1069M. doi:10.1038/35016611. PMID 10890450. S2CID 13750159.
  • Shen X, Hong F, Nguyen VA, Gao B (September 2000). "IL-10 attenuates IFN-alpha-activated STAT1 in the liver: involvement of SOCS2 and SOCS3". FEBS Letters. 480 (2–3): 132–136. doi:10.1016/S0014-5793(00)01905-0. PMID 11034314. S2CID 84290049.
  • Eyckerman S, Verhee A, der Heyden JV, Lemmens I, Ostade XV, Vandekerckhove J, Tavernier J (December 2001). "Design and application of a cytokine-receptor-based interaction trap". Nature Cell Biology. 3 (12): 1114–1119. doi:10.1038/ncb1201-1114. PMID 11781573. S2CID 10228882.
  • Schultheis B, Carapeti-Marootian M, Hochhaus A, Weisser A, Goldman JM, Melo JV (March 2002). "Overexpression of SOCS-2 in advanced stages of chronic myeloid leukemia: possible inadequacy of a negative feedback mechanism". Blood. 99 (5): 1766–1775. doi:10.1182/blood.V99.5.1766. PMID 11861294.
  • Blumenstein M, Bowen-Shauver JM, Keelan JA, Mitchell MD (March 2002). "Identification of suppressors of cytokine signaling (SOCS) proteins in human gestational tissues: differential regulation is associated with the onset of labor". The Journal of Clinical Endocrinology and Metabolism. 87 (3): 1094–1097. doi:10.1210/jcem.87.3.8463. PMID 11889171.
  • Biener E, Maurice S, Sandowski Y, Cohen Y, Gusakowsky EE, Hooghe R, et al. (July 2002). "Recombinant human CIS2 (SOCS2) protein: subcloning, expression, purification, and characterization". Protein Expression and Purification. 25 (2): 305–312. doi:10.1016/S1046-5928(02)00013-X. PMID 12135564.
  • v
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  • 2c9w: CRYSTAL STRUCTURE OF SOCS-2 IN COMPLEX WITH ELONGIN-B AND ELONGIN-C AT 1.9A RESOLUTION
    2c9w: CRYSTAL STRUCTURE OF SOCS-2 IN COMPLEX WITH ELONGIN-B AND ELONGIN-C AT 1.9A RESOLUTION

External links

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