Ribosomal protein S19


Ribosomal protein S19

Ribosomal protein S19, also known as RPS19, is a human gene.cite web | title = Entrez Gene: RPS19 ribosomal protein S19| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6223| accessdate = ]

PBB_Summary
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summary_text = Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function. Higher expression levels of this gene in some primary colon carcinomas compared to matched normal colon tissues has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.cite web | title = Entrez Gene: RPS19 ribosomal protein S19| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6223| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Wool IG, Chan YL, Glück A |title=Structure and evolution of mammalian ribosomal proteins. |journal=Biochem. Cell Biol. |volume=73 |issue= 11-12 |pages= 933–47 |year= 1996 |pmid= 8722009 |doi=
*cite journal | author=Morimoto K, Lin S, Sakamoto K |title=The functions of RPS19 and their relationship to Diamond-Blackfan anemia: a review. |journal=Mol. Genet. Metab. |volume=90 |issue= 4 |pages= 358–62 |year= 2007 |pmid= 17178250 |doi= 10.1016/j.ymgme.2006.11.004
*cite journal | author=Yamamoto T |title=Roles of the ribosomal protein S19 dimer and the C5a receptor in pathophysiological functions of phagocytic leukocytes. |journal=Pathol. Int. |volume=57 |issue= 1 |pages= 1–11 |year= 2007 |pmid= 17199736 |doi= 10.1111/j.1440-1827.2007.02049.x
*cite journal | author=Kondoh N, Schweinfest CW, Henderson KW, Papas TS |title=Differential expression of S19 ribosomal protein, laminin-binding protein, and human lymphocyte antigen class I messenger RNAs associated with colon carcinoma progression and differentiation. |journal=Cancer Res. |volume=52 |issue= 4 |pages= 791–6 |year= 1992 |pmid= 1339304 |doi=
*cite journal | author=Vladimirov SN, Ivanov AV, Karpova GG, "et al." |title=Characterization of the human small-ribosomal-subunit proteins by N-terminal and internal sequencing, and mass spectrometry. |journal=Eur. J. Biochem. |volume=239 |issue= 1 |pages= 144–9 |year= 1996 |pmid= 8706699 |doi=
*cite journal | author=Kenmochi N, Kawaguchi T, Rozen S, "et al." |title=A map of 75 human ribosomal protein genes. |journal=Genome Res. |volume=8 |issue= 5 |pages= 509–23 |year= 1998 |pmid= 9582194 |doi=
*cite journal | author=Draptchinskaia N, Gustavsson P, Andersson B, "et al." |title=The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. |journal=Nat. Genet. |volume=21 |issue= 2 |pages= 169–75 |year= 1999 |pmid= 9988267 |doi= 10.1038/5951
*cite journal | author=Willig TN, Draptchinskaia N, Dianzani I, "et al." |title=Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression. |journal=Blood |volume=94 |issue= 12 |pages= 4294–306 |year= 2000 |pmid= 10590074 |doi=
*cite journal | author=Matsson H, Klar J, Draptchinskaia N, "et al." |title=Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia. |journal=Hum. Genet. |volume=105 |issue= 5 |pages= 496–500 |year= 2000 |pmid= 10598818 |doi=
*cite journal | author=Tentler D, Gustavsson P, Elinder G, "et al." |title=A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome. |journal=J. Med. Genet. |volume=37 |issue= 2 |pages= 128–31 |year= 2000 |pmid= 10662814 |doi=
*cite journal | author=Ramenghi U, Campagnoli MF, Garelli E, "et al." |title=Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. |journal=Blood Cells Mol. Dis. |volume=26 |issue= 5 |pages= 417–22 |year= 2001 |pmid= 11112378 |doi= 10.1006/bcmd.2000.0324
*cite journal | author=Nishimura T, Horino K, Nishiura H, "et al." |title=Apoptotic cells of an epithelial cell line, AsPC-1, release monocyte chemotactic S19 ribosomal protein dimer. |journal=J. Biochem. |volume=129 |issue= 3 |pages= 445–54 |year= 2001 |pmid= 11226885 |doi=
*cite journal | author=Soulet F, Al Saati T, Roga S, "et al." |title=Fibroblast growth factor-2 interacts with free ribosomal protein S19. |journal=Biochem. Biophys. Res. Commun. |volume=289 |issue= 2 |pages= 591–6 |year= 2002 |pmid= 11716516 |doi= 10.1006/bbrc.2001.5960
*cite journal | author=Shibuya Y, Shiokawa M, Nishiura H, "et al." |title=Identification of receptor-binding sites of monocyte chemotactic S19 ribosomal protein dimer. |journal=Am. J. Pathol. |volume=159 |issue= 6 |pages= 2293–301 |year= 2001 |pmid= 11733378 |doi=
*cite journal | author=Li B, Sun M, He B, "et al." |title=Identification of differentially expressed genes in human uterine leiomyomas using differential display. |journal=Cell Res. |volume=12 |issue= 1 |pages= 39–45 |year= 2004 |pmid= 11942409 |doi= 10.1038/sj.cr.7290108
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Da Costa L, Tchernia G, Gascard P, "et al." |title=Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology. |journal=Blood |volume=101 |issue= 12 |pages= 5039–45 |year= 2004 |pmid= 12586610 |doi= 10.1182/blood-2002-12-3878
*cite journal | author=Shrestha A, Shiokawa M, Nishimura T, "et al." |title=Switch moiety in agonist/antagonist dual effect of S19 ribosomal protein dimer on leukocyte chemotactic C5a receptor. |journal=Am. J. Pathol. |volume=162 |issue= 4 |pages= 1381–8 |year= 2003 |pmid= 12651630 |doi=
*cite journal | author=Proust A, Da Costa L, Rince P, "et al." |title=Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 gene. |journal=Hematol. J. |volume=4 |issue= 2 |pages= 132–6 |year= 2003 |pmid= 12750732 |doi= 10.1038/sj.thj.6200230

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