Biology:Apoptosis-antagonizing transcription factor

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Protein AATF is a protein that in humans is encoded by the AATF gene.[1][2][3]

Function

The protein encoded by this gene was identified on the basis of its interaction with MAP3K12/DLK, a protein kinase known to be involved in the induction of cell apoptosis. This gene product contains a leucine zipper, which is a characteristic motif of transcription factors, and was shown to exhibit strong transactivation activity when fused to Gal4 DNA binding domain. Overexpression of this gene interfered with MAP3K12 induced apoptosis.[3]

Interactions

Apoptosis-antagonizing transcription factor has been shown to interact with:

References

  1. "Identification of novel transcription factor-like gene from human intestinal cells". Biochemical and Biophysical Research Communications 276 (2): 660–6. Sep 2000. doi:10.1006/bbrc.2000.3480. PMID 11027528. 
  2. 2.0 2.1 2.2 "Identification of a novel partner of RNA polymerase II subunit 11, Che-1, which interacts with and affects the growth suppression function of Rb". FASEB Journal 14 (7): 904–12. May 2000. doi:10.1096/fasebj.14.7.904. PMID 10783144. 
  3. 3.0 3.1 "Entrez Gene: AATF apoptosis antagonizing transcription factor". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26574. 
  4. "AATF inhibits aberrant production of amyloid beta peptide 1-42 by interacting directly with Par-4". The Journal of Biological Chemistry 279 (6): 4596–603. Feb 2004. doi:10.1074/jbc.M309811200. PMID 14627703. 
  5. "Che-1 affects cell growth by interfering with the recruitment of HDAC1 by Rb". Cancer Cell 2 (5): 387–99. Nov 2002. doi:10.1016/s1535-6108(02)00182-4. PMID 12450794. 
  6. "Che-1 arrests human colon carcinoma cell proliferation by displacing HDAC1 from the p21WAF1/CIP1 promoter". The Journal of Biological Chemistry 278 (38): 36496–504. Sep 2003. doi:10.1074/jbc.M306694200. PMID 12847090. 

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.