Biology:MYST4

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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

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