Phospho-GTF2I (Y248) Antibody

1. demonstrate a marked prevalence of a thymoma-specific mutated oncogene, GTF2I PMID: 29438696
2. we identified largest-ever effect on Asian rheumatoid arthritis across human non-HLA regions at GTF2I by heterogeneity mapping followed by replication studies, and pinpointed a possible causal variant PMID: 27272985
3. the frequency of GTF2I mutation is higher in more indolent TETs and correlated with better prognosis. PMID: 28676218
4. GTF2I/Gtf2i, its physiologic role in human disorders was relatively unknown until recently. Novel studies show that it is involved in an array of human diseases including neurocognitive disorders, systemic lupus erythematosus (SLE), and cancer. PMID: 28461154
5. the results reported here support a model whereby common genetic variation in GTF2I mediates human sociality and anxiety via effects on oxytocin reactivity. PMID: 28424317
6. GTF2I mutations common in thymic epithelial tumors are not present/uncommon in hematological malignancies. PMID: 28982856
7. a new BRAF fusion in pilocytic astrocytoma PMID: 28448514
8. A common polymorphism in the Williams syndrome gene GTF2I associated with reduced social anxiety predicts decreased threat-related amygdala reactivity, which mediates an association between genotype and increased warmth in women. PMID: 26853120
9. We identified rs117026326 on GTF2I with GWAS significance (P = 1.10 x 10(-15)) and rs13079920 on RBMS3 with suggestive significance (P = 2.90 x 10(-5)) associating with Primary Sjogren's syndrome in women. PMID: 27503288
10. The authors found that human adenovirus 5 infection or ectopic E4-ORF3 expression leads to SUMOylation of TFII-I that precedes a rapid decline in TFII-I protein levels. PMID: 26814176
11. A novel interaction between TFII-I and Mdm2 with a negative effect on TFII-I transcriptional activity has been documented. PMID: 26656605
12. Copy-number variation in the general transcription factor gene, GTF2I is associated with gene-dose-dependent anxiety in mouse models and in both Williams syndrome and Dup7. PMID: 26285132
13. show that SUMOylation is critical for TFII-I to promote cell proliferation and colony formation. Our findings contribute to understanding the role of SUMOylation in liver cancer development PMID: 25869096
14. Study demonstrates a significant association between SLE in Chinese Han population and the GTF2I rs117026326 T allele/GTF2IRD1 rs4717901 C allele. PMID: 26320362
15. Rather than contributing positively to promoter activity, a putative initiator element at the transcription start site acts as a target for negative regulation imposed on the L4P promoter of human adenovirus Type 5 by cellular TFII-I. PMID: 25926634
16. Findings implicate the GTF2I gene in the neurogenetic basis of social communication and social anxiety, both in Williams syndrome and among individuals in healthy populations PMID: 25429715
17. TFII-I bridges Proliferating Cell Nuclear Antigen and Polzeta to promote Translesion synthesis PMID: 24922507
18. The GTF2I rs117026326 polymorphism is associated with anti-SSA-positive primary Sjogren's syndrome. PMID: 25480810
19. A proportion of this transcriptional dysregulation is caused by dosage imbalances in GTF2I, which encodes a key transcription factor at 7q11.23 that is associated with the LSD1 repressive chromatin complex and silences its dosage-sensitive targets. PMID: 25501393
20. GTF2I mutation correlated with better survival. PMID: 24974848
21. Results reveal novel mechanisms by which TFII-I and DBC1 can modulate cellular fate by affecting cell-cycle control as well as the homologous recombination pathway. PMID: 24231951
22. Our findings suggest the GTF2i gene is important in the etiology of autism in individuals with this duplication and in non-duplication cases with severe social interaction problems and repetitive behaviors. PMID: 22048961
23. GTF2I duplication results in separation anxiety in mice and humans PMID: 22578324
24. CLIP2 haploinsufficiency by itself does not lead to the physical or cognitive characteristics of the Williams-Beuren syndrome; GTF2IRD1 and GTF2I are the main genes causing the cognitive defects PMID: 22608712
25. TFII-I gene deletion may explain the Williams-Beuren syndrome phenotype because it acts as a negative regulator of TRPC3 expression in human B lymphocytes. PMID: 22566418
26. These data indicate that an E-box motif (RBE1) within the core promoter in the long terminal repeat of HIV-1 is a bona fide binding site for the RBF-2 transcription factor complex USF1, USF2, and TFII-I. PMID: 21813151
27. Data demonstrate that not only does cell surface GRP78 regulate apoptosis, but it also regulates Ca(2+) homeostasis by controlling cell surface localization of TFII-I. PMID: 21503958
28. Data show that Igh 3' enhancer-bound OCA-B and promoter-bound TFII-I mediate promoter-enhancer interactions, in both cis and trans, that are important for Igh transcription. PMID: 21549311
29. These data indicate that Gtf2i is involved in several aspects of embryonic development and the development of social neurocircuitry and that GTF2I haploinsufficiency could be a contributor to the hypersociability in WBS patients. PMID: 21328569
30. TFII-I may modulate the cellular functions of BRCA1. PMID: 21407215
31. functional hemizygosity for the GTF2I and GTF2IRD1 genes is the main cause of the neurocognitive profile and some aspects of the gestalt phenotype of Williams-Beuren syndrome PMID: 19897463
32. G-kinase I beta interacted specifically with TFII-I, an unusual transcriptional regulator that associates with multiple proteins to modulate both basal and signal-induced transcription PMID: 12082086
33. GTF2IRD1 and GTF2I have roles in causing deficits on visual spatial functioning PMID: 12865760
34. Comparison of these five families with reports of other individuals with partial deletions of the WS region most strongly implicates GTF2I in the mental retardation of WS. PMID: 14556246
35. TFII-I is required for optimal induction of Grp78 by ER stress PMID: 15664986
36. These results demonstrate that USF1/USF2 and TFII-I interact cooperatively at the upstream RBEIII element and are necessary for the induction of latent HIV-1 in response to T-cell activation signals. PMID: 15767439
37. human VEGFR-2 promoter is functionally counter-regulated by TFII-I and TFII-IRD1. PMID: 15941713
38. cGMP-dependent protein kinase Ibeta binds to TFII-I and IRAG through a common interaction motif PMID: 16166082
39. TFII-I is recruited to the cyclin D1 promoter and transcriptionally activates this gene. PMID: 16314517
40. TFII-I directly interacts with Bright through amino acids in Bright's protein interaction domain PMID: 16738337
41. The data suggest that TFII-I and USF regulate chromatin structure accessibility and recruitment of transcription complexes in the beta-globin gene locus. PMID: 16943425
42. observations suggest a model in which TFII-I suppresses agonist-induced calcium entry by competing with TRPC3 for binding to phospholipase C-gamma PMID: 17023658
43. TFII-I, PARP1, and SFPQ proteins, each previously implicated in gene regulation, form a complex controlling transcription of DYX1C1. Allelic differences in the promoter or 5'UTR of DYX1C1 may affect factor binding and thus regulation of the gene. PMID: 18445785
44. Bioinformatics and microarray results were combined to identify TFII-I downstream targets in the vertebrate genome. PMID: 18579769
45. These results demonstrate an essential role of TFII-I bound at an upstream LTR element for viral replication. PMID: 18976654
46. alpha(2)-macroglobulin induced increase in GRP78 synthesis is caused by transcriptional upregulation of TFII-I PMID: 19097122
47. analyzed promoter regions of TFII-I genes and described their additional exons, as well as tested tissue specificity of both previously reported and novel alternatively spliced isoforms PMID: 19111598
48. Results suggest that TFII-I appears to have distinct roles in distinct phases of the mammalian cell cycle. PMID: 19182516
49. these results provide an initial step in understanding the biological role of Itk-TFII-I signaling in T-cell function. PMID: 19701889
50. TFII-I plays an inhibitory role in regulating genes that are essential in osteogenesis and intersects with the bone-specific transcription factor Runx2 and the retinoblastoma protein, pRb. PMID: 19880526

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HGNC: 4659

OMIM: 601679

KEGG: hsa:2969

STRING: 9606.ENSP00000322542

UniGene: Hs.647041