STC2: Difference between revisions

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| summary_text = This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The encoded protein has 10 of its 15 cysteine residues conserved among stanniocalcin family members and is phosphorylated by casein kinase 2 exclusively on its serine residues. Its C-terminus contains a cluster of histidine residues which may interact with metal ions.<ref name="entrez">{{cite web | title = Entrez Gene: STC2 stanniocalcin 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8614| accessdate = }}</ref>
| summary_text = This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The encoded protein has 10 of its 15 cysteine residues conserved among stanniocalcin family members and is phosphorylated by casein kinase 2 exclusively on its serine residues. Its C-terminus contains a cluster of histidine residues which may interact with metal ions.<ref name="entrez">{{cite web | title = Entrez Gene: STC2 stanniocalcin 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8614| accessdate = }}</ref>
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The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/[[phosphate homeostasis]]. Constitutive overexpression of human stanniocalcin 2 in mice resulted in pre- and postnatal growth restriction, reduced bone and skeletal muscle growth, and organomegaly. Expression of this gene is induced by estrogen and altered in some breast cancers.<ref name="entrez">{{cite web | title = Entrez Gene: STC2 stanniocalcin 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8614| accessdate = }}</ref> Stanniocalcin 2 may suppress P<sub>i</sub> cotransport.<ref name=Murer>{{ cite journal |author=Murer H, Hernando N, Forster I, Biber J |title=Proximal tubular phosphate reabsorption: molecular mechanisms |journal=Physiol Rev. |year=2000 |month=Oct |volume=80 |issue=4 |pages=1373-409 |pmid=11015617 }}</ref>
The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/[[phosphate homeostasis]]. Constitutive overexpression of human stanniocalcin 2 in mice resulted in pre- and postnatal growth restriction, reduced bone and skeletal muscle growth, and organomegaly. Expression of this gene is induced by estrogen and altered in some breast cancers.<ref name="entrez">{{cite web | title = Entrez Gene: STC2 stanniocalcin 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8614| accessdate = }}</ref> Stanniocalcin 2 may suppress P<sub>i</sub> cotransport.<ref name=Murer>{{ cite journal |author=Murer H, Hernando N, Forster I, Biber J |title=Proximal tubular phosphate reabsorption: molecular mechanisms |journal=Physiol Rev. |year=2000 |month=Oct |volume=80 |issue=4 |pages=1373-409 |pmid=11015617 }}</ref>


Revision as of 19:49, 8 September 2009


Stanniocalcin 2
Identifiers
Symbols STC2 ; STC-2; STCRP
External IDs Template:OMIM5 Template:MGI HomoloGene: 2753
RNA expression pattern
File:PBB GE STC2 203439 s at tn.png
File:PBB GE STC2 203438 at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

Stanniocalcin 2, also known as STC2, is a human gene.[1] This gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The encoded protein has 10 of its 15 cysteine residues conserved among stanniocalcin family members and is phosphorylated by casein kinase 2 exclusively on its serine residues. Its C-terminus contains a cluster of histidine residues which may interact with metal ions.[1] The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport, cell metabolism, or cellular calcium/phosphate homeostasis. Constitutive overexpression of human stanniocalcin 2 in mice resulted in pre- and postnatal growth restriction, reduced bone and skeletal muscle growth, and organomegaly. Expression of this gene is induced by estrogen and altered in some breast cancers.[1] Stanniocalcin 2 may suppress Pi cotransport.[2]

References

  1. ↑ 1.0 1.1 1.2 "Entrez Gene: STC2 stanniocalcin 2".
  2. ↑ Murer H, Hernando N, Forster I, Biber J (2000). "Proximal tubular phosphate reabsorption: molecular mechanisms". Physiol Rev. 80 (4): 1373–409. PMID 11015617. Unknown parameter |month= ignored (help)

Further reading

  • Chang AC, Reddel RR (1998). "Identification of a second stanniocalcin cDNA in mouse and human: stanniocalcin 2". Mol. Cell. Endocrinol. 141 (1–2): 95–9. PMID 9723890.
  • Ishibashi K, Miyamoto K, Taketani Y; et al. (1998). "Molecular cloning of a second human stanniocalcin homologue (STC2)". Biochem. Biophys. Res. Commun. 250 (2): 252–8. doi:10.1006/bbrc.1998.9300. PMID 9753616.
  • DiMattia GE, Varghese R, Wagner GF (1999). "Molecular cloning and characterization of stanniocalcin-related protein". Mol. Cell. Endocrinol. 146 (1–2): 137–40. PMID 10022771.
  • Moore EE, Kuestner RE, Conklin DC; et al. (1999). "Stanniocalcin 2: characterization of the protein and its localization to human pancreatic alpha cells". Horm. Metab. Res. 31 (7): 406–14. PMID 10450831.
  • Jellinek DA, Chang AC, Larsen MR; et al. (2001). "Stanniocalcin 1 and 2 are secreted as phosphoproteins from human fibrosarcoma cells". Biochem. J. 350 Pt 2: 453–61. PMID 10947959.
  • Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.
  • Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Beausoleil SA, Jedrychowski M, Schwartz D; et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMID 15302935.
  • Gagliardi AD, Kuo EY, Raulic S; et al. (2005). "Human stanniocalcin-2 exhibits potent growth-suppressive properties in transgenic mice independently of growth hormone and IGFs". Am. J. Physiol. Endocrinol. Metab. 288 (1): E92–105. doi:10.1152/ajpendo.00268.2004. PMID 15367391.
  • Luo CW, Pisarska MD, Hsueh AJ (2005). "Identification of a stanniocalcin paralog, stanniocalcin-2, in fish and the paracrine actions of stanniocalcin-2 in the mammalian ovary". Endocrinology. 146 (1): 469–76. doi:10.1210/en.2004-1197. PMID 15486227.
  • Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.
  • Stelzl U, Worm U, Lalowski M; et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. PMID 16169070.
  • Otsuki T, Ota T, Nishikawa T; et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. 12 (2): 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.
  • Esseghir S, Kennedy A, Seedhar P; et al. (2007). "Identification of NTN4, TRA1, and STC2 as prognostic markers in breast cancer in a screen for signal sequence encoding proteins". Clin. Cancer Res. 13 (11): 3164–73. doi:10.1158/1078-0432.CCR-07-0224. PMID 17545519.
  • Ichikawa T, Horie-Inoue K, Ikeda K; et al. (2007). "Vitamin K2 induces phosphorylation of protein kinase A and expression of novel target genes in osteoblastic cells". J. Mol. Endocrinol. 39 (4): 239–47. doi:10.1677/JME-07-0048. PMID 17909264.

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