PIAS4

Protein inhibitor of activated STAT, 4, also known as PIAS4, is a human gene. [cite web | title = Entrez Gene: PIAS4 Protein inhibitor of activated STAT, 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51588| accessdate = ]

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References

Further reading

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*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Liu B, Liao J, Rao X, "et al." |title=Inhibition of Stat1-mediated gene activation by PIAS1. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 18 |pages= 10626–31 |year= 1998 |pmid= 9724754 |doi=
*cite journal | author=Liu B, Gross M, ten Hoeve J, Shuai K |title=A transcriptional corepressor of Stat1 with an essential LXXLL signature motif. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=98 |issue= 6 |pages= 3203–7 |year= 2001 |pmid= 11248056 |doi= 10.1073/pnas.051489598
*cite journal | author=Nelson V, Davis GE, Maxwell SA |title=A putative protein inhibitor of activated STAT (PIASy) interacts with p53 and inhibits p53-mediated transactivation but not apoptosis. |journal=Apoptosis |volume=6 |issue= 3 |pages= 221–34 |year= 2001 |pmid= 11388671 |doi=
*cite journal | author=Gross M, Liu B, Tan J, "et al." |title=Distinct effects of PIAS proteins on androgen-mediated gene activation in prostate cancer cells. |journal=Oncogene |volume=20 |issue= 29 |pages= 3880–7 |year= 2001 |pmid= 11439351 |doi= 10.1038/sj.onc.1204489
*cite journal | author=Sachdev S, Bruhn L, Sieber H, "et al." |title=PIASy, a nuclear matrix-associated SUMO E3 ligase, represses LEF1 activity by sequestration into nuclear bodies. |journal=Genes Dev. |volume=15 |issue= 23 |pages= 3088–103 |year= 2001 |pmid= 11731474 |doi=
*cite journal | author=Ohmine K, Ota J, Ueda M, "et al." |title=Characterization of stage progression in chronic myeloid leukemia by DNA microarray with purified hematopoietic stem cells. |journal=Oncogene |volume=20 |issue= 57 |pages= 8249–57 |year= 2002 |pmid= 11781839 |doi= 10.1038/sj.onc.1205029
*cite journal | author=Tan JA, Hall SH, Hamil KG, "et al." |title=Protein inhibitors of activated STAT resemble scaffold attachment factors and function as interacting nuclear receptor coregulators. |journal=J. Biol. Chem. |volume=277 |issue= 19 |pages= 16993–7001 |year= 2002 |pmid= 11877418 |doi= 10.1074/jbc.M109217200
*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=Subramanian L, Benson MD, Iñiguez-Lluhí JA |title=A synergy control motif within the attenuator domain of CCAAT/enhancer-binding protein alpha inhibits transcriptional synergy through its PIASy-enhanced modification by SUMO-1 or SUMO-3. |journal=J. Biol. Chem. |volume=278 |issue= 11 |pages= 9134–41 |year= 2003 |pmid= 12511558 |doi= 10.1074/jbc.M210440200
*cite journal | author=Dahle Ø, Andersen TØ, Nordgård O, "et al." |title=Transactivation properties of c-Myb are critically dependent on two SUMO-1 acceptor sites that are conjugated in a PIASy enhanced manner. |journal=Eur. J. Biochem. |volume=270 |issue= 6 |pages= 1338–48 |year= 2003 |pmid= 12631292 |doi=
*cite journal | author=Yamamoto H, Ihara M, Matsuura Y, Kikuchi A |title=Sumoylation is involved in beta-catenin-dependent activation of Tcf-4. |journal=EMBO J. |volume=22 |issue= 9 |pages= 2047–59 |year= 2003 |pmid= 12727872 |doi= 10.1093/emboj/cdg204
*cite journal | author=Lee PS, Chang C, Liu D, Derynck R |title=Sumoylation of Smad4, the common Smad mediator of transforming growth factor-beta family signaling. |journal=J. Biol. Chem. |volume=278 |issue= 30 |pages= 27853–63 |year= 2003 |pmid= 12740389 |doi= 10.1074/jbc.M301755200
*cite journal | author=Chun TH, Itoh H, Subramanian L, "et al." |title=Modification of GATA-2 transcriptional activity in endothelial cells by the SUMO E3 ligase PIASy. |journal=Circ. Res. |volume=92 |issue= 11 |pages= 1201–8 |year= 2003 |pmid= 12750312 |doi= 10.1161/01.RES.0000076893.70898.36
*cite journal | author=Imoto S, Sugiyama K, Muromoto R, "et al." |title=Regulation of transforming growth factor-beta signaling by protein inhibitor of activated STAT, PIASy through Smad3. |journal=J. Biol. Chem. |volume=278 |issue= 36 |pages= 34253–8 |year= 2003 |pmid= 12815042 |doi= 10.1074/jbc.M304961200
*cite journal | author=Galleguillos D, Vecchiola A, Fuentealba JA, "et al." |title=PIASgamma represses the transcriptional activation induced by the nuclear receptor Nurr1. |journal=J. Biol. Chem. |volume=279 |issue= 3 |pages= 2005–11 |year= 2004 |pmid= 14559918 |doi= 10.1074/jbc.M308113200
*cite journal | author=Gross M, Yang R, Top I, "et al." |title=PIASy-mediated repression of the androgen receptor is independent of sumoylation. |journal=Oncogene |volume=23 |issue= 17 |pages= 3059–66 |year= 2004 |pmid= 14981544 |doi= 10.1038/sj.onc.1207443
*cite journal | author=Zoumpoulidou G, Jones MC, Fernandez de Mattos S, "et al." |title=Convergence of interferon-gamma and progesterone signaling pathways in human endometrium: role of PIASy (protein inhibitor of activated signal transducer and activator of transcription-y). |journal=Mol. Endocrinol. |volume=18 |issue= 8 |pages= 1988–99 |year= 2005 |pmid= 15155784 |doi= 10.1210/me.2003-0467
*cite journal | author=Imoto S, Sugiyama K, Yamamoto T, Matsuda T |title=The RING domain of PIASy is involved in the suppression of bone morphogenetic protein-signaling pathway. |journal=Biochem. Biophys. Res. Commun. |volume=319 |issue= 1 |pages= 275–82 |year= 2004 |pmid= 15158472 |doi= 10.1016/j.bbrc.2004.04.161

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