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SERPINE1 mRNA binding protein 1

PAIRBP1, RDA288, SERBP1, CGI-55
Top mentioned proteins: MPR, Plasminogen, V1a, DG-6, ACID
Papers on PAIRBP1
Gene expression profile of circulating CD34(+) cells and granulocytes in chronic myeloid leukemia.
New
Puri et al., Belgrade, Serbia. In Blood Cells Mol Dis, Dec 2015
The 41 and 39 genes were significantly upregulated in CML CD34(+) cells (HINT1, TXN, SERBP1) and granulocytes, respectively.
SERBP1 Is a Component of the Liver Receptor Homologue-1 Transcriptional Complex.
New
Griffin et al., Jupiter, United States. In J Proteome Res, Dec 2015
SERBP1 and ILF3 were identified as LRH1 interacting partners by both Western blot and MS/MS analysis.
SERBP1 affects homologous recombination-mediated DNA repair by regulation of CtIP translation during S phase.
New
Choi et al., Suwŏn, South Korea. In Nucleic Acids Res, Aug 2015
Here, we show that Serpine mRNA binding protein 1 (SERBP1) regulates CtIP expression at the translational level in S phase.
Ki-1/57 and CGI-55 ectopic expression impact cellular pathways involved in proliferation and stress response regulation.
Kobarg et al., Campinas, Brazil. In Biochim Biophys Acta, 2014
Ki-1/57 (HABP4) and CGI-55 (SERBP1) are regulatory proteins and paralogs with 40.7% amino acid sequence identity and 67.4% similarity.
Expression and localization of progesterone receptor membrane component 1 and 2 and serpine mRNA binding protein 1 in the bovine corpus luteum during the estrous cycle and the first trimester of pregnancy.
Kotwica et al., Olsztyn, Poland. In Theriogenology, 2014
The aim of this study was to evaluate the mRNA and protein expression and the localization of progesterone receptor membrane component 1 (PGRMC1), PGRMC2, and the PGRMC1 partner serpine mRNA binding protein 1 (SERBP1) in the bovine CL on Days 2 to 5, 6 to 10, 11 to 16, and 17 to 20 of the estrous cycle as well as during Weeks 3 to 5, 6 to 8, and 9 to 12 of pregnancy (n = 5-6 per each period).
Low SOX17 expression is a prognostic factor and drives transcriptional dysregulation and esophageal cancer progression.
Wang et al., Zhengzhou, China. In Int J Cancer, 2014
Using quantitative chromatin immunoprecipitation-PCR and promoter activity assays, we confirmed that MACC1, MALAT1, NBN, NFAT5, CSNK1A1, FN1 and SERBP1 genes were suppressed by SOX17 via the SRY binding-mediated transcriptional regulation.
Localization of SERBP1 in stress granules and nucleoli.
Li et al., T'ai-chung-shih, Taiwan. In Febs J, 2014
SERPINE1 mRNA-binding protein 1 (SERBP1) is an arginine-methylated RNA-binding protein whose modification affects protein interaction and intracellular localization.
Expression of progesterone receptor membrane component (PGRMC) 1 and 2, serpine mRNA binding protein 1 (SERBP1) and nuclear progesterone receptor (PGR) in the bovine endometrium during the estrous cycle and the first trimester of pregnancy.
Kotwica et al., Olsztyn, Poland. In Reprod Biol, 2013
The aim of this study was to determine the mRNA and protein expression for PGRMC1, PGRMC2, SERBP1 and PGR within the bovine endometrium during the estrous cycle and the first trimester of pregnancy.
Plasminogen activator inhibitor 1 RNA-binding protein interacts with progesterone receptor membrane component 1 to regulate progesterone's ability to maintain the viability of spontaneously immortalized granulosa cells and rat granulosa cells.
Lodde et al., Farmington, United States. In Biol Reprod, 2013
PGRMC1 interacts with plasminogen activator inhibitor 1 RNA-binding protein (PAIRBP1), but the functional significance of this interaction is unknown.
Reverse engineering of modified genes by Bayesian network analysis defines molecular determinants critical to the development of glioblastoma.
Roy et al., Miami, United States. In Plos One, 2012
Genes found to be most influential to development of the highest grade of astrocytoma, Glioblastoma multiforme were: COL4A1, EGFR, BTF3, MPP2, RAB31, CDK4, CD99, ANXA2, TOP2A, and SERBP1.
A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumption.
Solter et al., Singapore, Singapore. In Plos One, 2012
Here, we report that, SPINDLIN1 (SPIN1), a maternal protein containing Tudor-like domains, interacts with a known mRNA-binding protein SERBP1, and is involved in regulating maternal transcripts to control meiotic resumption.
Posttranscriptional regulation of expression of plasminogen activator inhibitor type-1 by sphingosine 1-phosphate in HepG2 liver cells.
Fujii et al., Nagoya, Japan. In Biochim Biophys Acta, 2012
SERPINE1 mRNA binding protein (SERBP1) and ARE3 in the 3'-UTR were involved in the posttranscriptional regulation by S1P.
Progesterone directly and rapidly inhibits GnRH neuronal activity via progesterone receptor membrane component 1.
Wray et al., Bethesda, United States. In Endocrinology, 2012
Receptors in the progestin/adipoQ receptor family (PAQR), as well as progesterone receptor membrane component 1 (PgRMC1) and its partner serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1) mRNA binding protein 1 (SERBP1), have been shown to mediate rapid progestin actions in various tissues, including the brain.
Protein arginine methylation of SERBP1 by protein arginine methyltransferase 1 affects cytoplasmic/nuclear distribution.
GeneRIF
Li et al., T'ai-chung-shih, Taiwan. In J Cell Biochem, 2012
The RG-rich and RGG box of SERBP1 is asymmetrically dimethylated by PRMT1 and the modification affects protein interaction and intracellular localization of the protein.
Overexpression of SERBP1 (Plasminogen activator inhibitor 1 RNA binding protein) in human breast cancer is correlated with favourable prognosis.
Dahl et al., Bonn, Germany. In Bmc Cancer, 2011
SERBP1, a protein that is supposed to regulate the stability of PAI-1 mRNA, may play a role in gynaecological cancers as well, since upregulation of SERBP1 was described in ovarian cancer recently.
Expression of progesterone receptor membrane component 1 and its partner serpine 1 mRNA binding protein in uterine and placental tissues of the mouse and human.
GeneRIF
Pru et al., Boston, United States. In Mol Cell Endocrinol, 2008
The aim of this study was to assess the expression, localization and hormonal regulation of two novel P(4) receptor candidates, P(4) receptor membrane component (PGRMC) 1 and PGRMC2, as well as the PGRMC1 partner Serpine 1 mRNA binding protein (SERBP1).
Expression analysis and RNA localization of PAI-RBP1 (SERBP1) in epithelial ovarian cancer: association with tumor progression.
GeneRIF
Sehouli et al., Berlin, Germany. In Gynecol Oncol, 2007
In ovarian cancer, PAI-RBP1 is significantly overexpressed in tumor epithelial cells, suggesting a biological role in tumor invasion and metastasis. Its expression is higher in advanced disease.
Ki-1/57 interacts with PRMT1 and is a substrate for arginine methylation.
GeneRIF
Kobarg et al., Campinas, Brazil. In Febs J, 2006
Has two conserved Gly/Arg-rich motif clusters (RGG/RXR box, where X is any amino acid) that may be substrates for arginine-methylation by protein arginine-methyltransferase-1 (PRMT1).
Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian population.
GeneRIF
Roisenberg et al., Porto Alegre, Brazil. In Blood Cells Mol Dis, 2006
The presence of the genotype risk factors alone does not seem to be associated with the development of preeclampsia even in the severe presentation form. PAI-1 gene polymorphisms on the development of the preeclampsia was indicated.
Multiplicity of progesterone's actions and receptors in the mammalian ovary.
Review
Peluso, Farmington, United States. In Biol Reprod, 2006
These pathways could be mediated by 1) the PGR localizing at or near the plasma membrane and activating SRC family kinases, 2) a membrane progestin receptor that responds to P4 by lowering intracellular cAMP and increasing MAPK 3/1 activity, and 3) a membrane receptor complex composed of serpine 1 mRNA binding protein (also known as PAIRBP1 or RDA288) and progesterone receptor membrane component 1. Ligand activation of this complex likely leads to an increase in protein kinase G activity, the maintenance of low basal intracellular free calcium, and the inhibition of granulosa and luteal cell mitosis and apoptosis.
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