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Atlas of Genetics and Cytogenetics in Oncology and Haematology OPEN ACCESS JOURNAL AT INIST-CNRS Gene Section Short Communication RGS17 (regulator of G-protein signaling 17) Chenguang Li, Lei Wang, Yihua Sun, Haiquan Chen Department of Thoracic Oncology, Fudan University Shanghai Cancer Center and Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China (CL, LW, YS, HC) Published in Atlas Database: October 2011 Online updated version : http://AtlasGeneticsOncology.org/Genes/RGS17ID47522ch6q25.html DOI: 10.4267/2042/47280 This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 France Licence. © 2012 Atlas of Genetics and Cytogenetics in Oncology and Haematology Identity Description Other names: RGS-17, RGSZ2, hRGS17 HGNC (Hugo): RGS17 Location: 6q25.2 The RGS17 protein consists of 210 amino acid residues. This gene encodes a member of the regulator of G-protein signaling family. This protein contains a conserved, 120 amino acid motif called the RGS domain and a cysteine-rich region. DNA/RNA Expression Description Widely expressed in human organs. The RGS17 gene spans over a region of 120 kbp DNA including 4 coding exons and 1 non-coding exon (exon 1). Localisation Transcription Function The RGS17 gene mRNA consists of about 1472 nucleotides with an open reading frame (ORF) of 633 bases. The protein attenuates the signaling activity of Gproteins by binding to activated, GTP-bound G alpha subunits and acting as a GTPase activating protein (GAP), increasing the rate of conversion of the GTP to GDP. RGS proteins are GTPase-activating proteins for Gi and Gq class G-alpha proteins. They accelerate transit through the cycle of GTP binding and hydrolysis and thereby accelerate signaling kinetics and termination. This hydrolysis allows the G alpha subunits to bind G beta/gamma subunit heterodimers, forming inactive G-protein heterotrimers, thereby terminating the signal. Its cellular localization has not been formally monitored to date. Pseudogene RGS17P1 regulator pseudogene 1. of G-protein signaling 17 Protein Note 210 amino acids; 24 kDa. Diagram of the RGS17 protein in scale. The numbers represent specific residues. The regions are RGS_RZ-like (Regulator of G protein signaling (RGS) domain found in the RZ protein), putative G-alpha interaction site. C: Carboxyl-terminal; N: Amino-terminal. Atlas Genet Cytogenet Oncol Haematol. 2012; 16(3) 216 RGS17 (regulator of G-protein signaling 17) Li C, et al. Homology Ovarian cancer The RGS17 gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, and zebrafish. Disease RGS2, RGS5, RGS10 and RGS17 transcripts are expressed at significantly lower levels in cells resistant to chemotherapy compared with parental, chemosensitive cells in ovarian cancer cells (Hooks et al., 2010). Prognosis RGS17 loss of expression contributes to the development of chemoresistance in ovarian cancer cells. Mutations Germinal No germline mutations in this gene have been reported. Somatic A synonymous-coding somatic mutations of this gene is reported in pancreas cancer at codon 166, P166P (COSMIC). References Implicated in James MA, Lu Y, Liu Y, Vikis HG, You M. RGS17, an overexpressed gene in human lung and prostate cancer, induces tumor cell proliferation through the cyclic AMP-PKACREB pathway. Cancer Res. 2009 Mar 1;69(5):2108-16 Various cancer Note Lung cancer, prostate cancer. Disease RSG17 is overexpressed in lung and prostate cancer (James et al., 2009). Expression of RGS17 is upregulated in 80% of lung tumors, and also up-regulated in prostate tumors. Overexpression of RGS17 induce and maintain cell proliferation. You M, Wang D, Liu P, Vikis H, James M, Lu Y, Wang Y, Wang M, Chen Q, Jia D, Liu Y, Wen W, Yang P, et al. Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene. Clin Cancer Res. 2009 Apr 15;15(8):2666-74 Hooks SB, Callihan P, Altman MK, Hurst JH, Ali MW, Murph MM. Regulators of G-Protein signaling RGS10 and RGS17 regulate chemoresistance in ovarian cancer cells. Mol Cancer. 2010 Nov 2;9:289 Lung cancer Sun Y, Fang R, Li C, Li L, Li F, Ye X, Chen H. Hsa-mir-182 suppresses lung tumorigenesis through down regulation of RGS17 expression in vitro. Biochem Biophys Res Commun. 2010 May 28;396(2):501-7 Disease hsa-mir-182 is involved in the down regulation of RGS17 expression through two conserved sites located in its 3' UTR region (Sun et al., 2010). Two SNPs in the first intron of RGS17 (rs4083914 and rs9479510) were found associated with familial lung cancer susceptibility (You et al., 2009). Atlas Genet Cytogenet Oncol Haematol. 2012; 16(3) This article should be referenced as such: Li C, Wang L, Sun Y, Chen H. RGS17 (regulator of G-protein signaling 17). Atlas Genet Cytogenet Oncol Haematol. 2012; 16(3):216-217. 217