GTF3C5

General transcription factor IIIC, polypeptide 5, 63kDa
Identifiers
Symbols GTF3C5 ; TFIIIC63; TFIIICepsilon; TFiiiC2-63
External IDs OMIM: 604890 MGI: 1917489 HomoloGene: 40806 GeneCards: GTF3C5 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 9328 70239
Ensembl ENSG00000148308 ENSMUSG00000026816
UniProt Q9Y5Q8 Q8R2T8
RefSeq (mRNA) NM_001122823 NM_001290484
RefSeq (protein) NP_001116295 NP_001277413
Location (UCSC) Chr 9:
133.03 – 133.06 Mb
Chr 2:
28.57 – 28.58 Mb
PubMed search

General transcription factor 3C polypeptide 5 is a protein that in humans is encoded by the GTF3C5 gene.[1][2]

Model organisms

Model organisms have been used in the study of GTF3C5 function. A conditional knockout mouse line, called Gtf3c5tm2a(KOMP)Wtsi[7][8] was generated as part of the International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists.[9][10][11]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[5][12] Twenty four tests were carried out on mutant mice and two significant abnormalities were observed.[5] No homozygous mutant embryos were identified during gestation, and therefore none survived until weaning. The remaining tests were carried out on heterozygous mutant adult mice; no additional significant abnormalities were observed in these animals.[5]

Interactions

GTF3C5 has been shown to interact with GTF3C2[1] and GTF3C4.[13]

References

  1. 1 2 Hsieh YJ, Wang Z, Kovelman R, Roeder RG (Jul 1999). "Cloning and characterization of two evolutionarily conserved subunits (TFIIIC102 and TFIIIC63) of human TFIIIC and their involvement in functional interactions with TFIIIB and RNA polymerase III". Mol. Cell. Biol. 19 (7): 4944–52. PMC 84305. PMID 10373544.
  2. "Entrez Gene: GTF3C5 general transcription factor IIIC, polypeptide 5, 63kDa".
  3. "Salmonella infection data for Gtf3c5". Wellcome Trust Sanger Institute.
  4. "Citrobacter infection data for Gtf3c5". Wellcome Trust Sanger Institute.
  5. 1 2 3 4 Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x.
  6. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  7. "International Knockout Mouse Consortium".
  8. "Mouse Genome Informatics".
  9. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
  10. Dolgin E (2011). "Mouse library set to be knockout". Nature 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  11. Collins FS, Rossant J, Wurst W (2007). "A mouse for all reasons". Cell 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
  12. van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biol. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353.
  13. Hsieh YJ, Kundu TK, Wang Z, Kovelman R, Roeder RG (Nov 1999). "The TFIIIC90 subunit of TFIIIC interacts with multiple components of the RNA polymerase III machinery and contains a histone-specific acetyltransferase activity". Mol. Cell. Biol. 19 (11): 7697–704. PMC 84812. PMID 10523658.

Further reading


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