Biology:MYST4

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

Histone acetyltransferase MYST4 is an enzyme that in humans is encoded by the MYST4 gene.[1][2][3]

Interactions

MYST4 has been shown to interact with RUNX2.[4]

Young Simpson syndrome

It has been demonstrated that de novo mutations in the gene MYST4 causes the Young Simpson syndrome and genitopatellar syndrome.[5][6][7][8]

References

  1. "Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro". DNA Res 4 (2): 141–50. Sep 1997. doi:10.1093/dnares/4.2.141. PMID 9205841. 
  2. "Identification of a human histone acetyltransferase related to monocytic leukemia zinc finger protein". J Biol Chem 274 (40): 28528–36. Nov 1999. doi:10.1074/jbc.274.40.28528. PMID 10497217. 
  3. "Entrez Gene: MYST4 MYST histone acetyltransferase (monocytic leukemia) 4". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=23522. 
  4. "MOZ and MORF histone acetyltransferases interact with the Runt-domain transcription factor Runx2". Oncogene 21 (17): 2729–40. Apr 2002. doi:10.1038/sj.onc.1205367. PMID 11965546. 
  5. "Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome.". American Journal of Human Genetics 90 (2): 282–9. Jan 18, 2012. doi:10.1016/j.ajhg.2011.11.023. PMID 22265014. 
  6. "Whole-Exome-Sequencing Identifies Mutations in Histone Acetyltransferase Gene KAT6B in Individuals with the Say-Barber-Biesecker Variant of Ohdo Syndrome". Am. J. Hum. Genet. 89 (5): 675–81. Nov 2011. doi:10.1016/j.ajhg.2011.10.008. PMID 22077973. 
  7. "Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome". American Journal of Human Genetics 90 (2): 282–9. Jan 2012. doi:10.1016/j.ajhg.2011.11.023. PMID 22265014. 
  8. "The KAT6B-related disorders Genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms.". Human Mutation 33 (11): 1520–5. Jun 19, 2012. doi:10.1002/humu.22141. PMID 22715153. 

Further reading

External links

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