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Gene Review

GABPAP  -  GA binding protein transcription factor,...

Homo sapiens

Synonyms: E4TF1, E4TF1B, GABPB1
 
 
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Disease relevance of GABPAP

  • The retinoblastoma binding factor 1 (RBF-1) site in RB gene promoter binds preferentially E4TF1, a member of the Ets transcription factors family [1].
  • E4TF1 was originally identified as one of the transcription factors responsible for adenovirus E4 gene transcription [2].
  • Regulation of human B19 parvovirus promoter expression by hGABP (E4TF1) transcription factor [3].
  • Promoter activity from a construct without a hGABP/E4TF1-binding site was markedly reduced in A549 human lung adenocarcinoma cells, but not in JKT-1 [4].
  • Differential response at the hGABP/E4TF1 site of retinoblastoma gene promoter in human testicular seminoma cells [4].
 

High impact information on GABPAP

  • E4TF1 has been purified to homogeneity from HeLa cells by sequence-specific DNA affinity chromatography and characterized [5].
  • This study provides evidence that the interaction between the two different subunits of E4TF1 is required for it to function as a transcription factor, and that one of the subunits binds to a specific DNA sequence and the other works as a modulator [5].
  • E4TF1 was purified, and the partial amino acid sequence of each subunit was determined [2].
  • The upstream region of the rat H+/K(+)-ATPase beta subunit gene contains direct repeat sequences and palindromes, potential binding sites for RNA polymerase II and E4TF1, and CACCC box sequences [6].
  • Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes [7].
 

Biological context of GABPAP

  • Regional mapping of two subunits of transcription factor E4TF1 to human chromosome [8].
  • Furthermore, promoter activity from a plasmid carrying a point mutation at the hGABP/E4TF1 site was reduced in A549 cells, but not altered in JKT-1 cells [4].
  • Several potential transcription regulatory motifs, such as Sp-1, E4TF1 and ATF binding sites, were identified in the 5'-flanking region [9].

References

  1. The retinoblastoma binding factor 1 (RBF-1) site in RB gene promoter binds preferentially E4TF1, a member of the Ets transcription factors family. Savoysky, E., Mizuno, T., Sowa, Y., Watanabe, H., Sawada, J., Nomura, H., Ohsugi, Y., Handa, H., Sakai, T. Oncogene (1994) [Pubmed]
  2. cDNA cloning of transcription factor E4TF1 subunits with Ets and notch motifs. Watanabe, H., Sawada, J., Yano, K., Yamaguchi, K., Goto, M., Handa, H. Mol. Cell. Biol. (1993) [Pubmed]
  3. Regulation of human B19 parvovirus promoter expression by hGABP (E4TF1) transcription factor. Vassias, I., Hazan, U., Michel, Y., Sawa, C., Handa, H., Gouya, L., Morinet, F. J. Biol. Chem. (1998) [Pubmed]
  4. Differential response at the hGABP/E4TF1 site of retinoblastoma gene promoter in human testicular seminoma cells. Shiraishi, T., Yoshida, T., Nakata, S., Horinaka, M., Wakada, M., Mizutani, Y., Miki, T., Sakai, T. Oncol. Rep. (2005) [Pubmed]
  5. Transcription factor E4TF1 contains two subunits with different functions. Watanabe, H., Wada, T., Handa, H. EMBO J. (1990) [Pubmed]
  6. The rat H+/K(+)-ATPase beta subunit gene and recognition of its control region by gastric DNA binding protein. Maeda, M., Oshiman, K., Tamura, S., Kaya, S., Mahmood, S., Reuben, M.A., Lasater, L.S., Sachs, G., Futai, M. J. Biol. Chem. (1991) [Pubmed]
  7. Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes. Tassone, F., Villard, L., Clancy, K., Gardiner, K. Gene (1999) [Pubmed]
  8. Regional mapping of two subunits of transcription factor E4TF1 to human chromosome. Sawada, J., Goto, M., Watanabe, H., Handa, H., Yoshida, M.C. Jpn. J. Cancer Res. (1995) [Pubmed]
  9. Genomic structure of the human UDP-GlcNAc:dolichol-P GlcNAc-1-P transferase gene. Regis, S., Dagnino, F., Caroli, F., Filocamo, M. DNA Seq. (2002) [Pubmed]
 
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