Double Homeobox Protein 4 (DUX4)
DUX4 is located within a D4Z4 repeat array in the subtelomeric region of chromosome 4q. The D4Z4 repeat is polymorphic in length; a similar D4Z4 repeat array has been identified on chromosome 10. Each D4Z4 repeat unit has an open reading frame (named DUX4) that contains two homeoboxes; the repeat-array and ORF is conserved in other mammals.
There was no evidence for transcription from standard cDNA libraries however RTPCR and in-vitro expression experiments indicate that the ORF is transcribed and the encoded protein has been reported to function as a transcriptional activator of paired-like homeodomain transcription factor 1 (PITX1). Contraction of the microsatellite repeat causes autosomal dominant facioscapulohumeral muscular dystrophy (FSHD).

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Double Homeobox Protein 4 (DUX4) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Double Homeobox Protein 4 (DUX4) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Double Homeobox Protein 4 (DUX4) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Double Homeobox Protein 4 (DUX4) CLIA Kit Customized Service Offer
n/a ELISA Kit for Double Homeobox Protein 4 (DUX4) ELISA Kit Customized Service Offer
  1. "Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element."Gene 236:25-32(1999) [PubMed] [Europe PMC] [Abstract]
  2. "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Nature 434:724-731(2005) [PubMed] [Europe PMC] [Abstract]
  3. "Intracellular trafficking and dynamics of double homeodomain proteins."Biochemistry 44:2378-2384(2005) [PubMed] [Europe PMC] [Abstract]
  4. "Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample."Clin. Genet. 75:550-555(2009) [PubMed] [Europe PMC] [Abstract]
  5. "Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene."PLoS Genet. 6:E1001181-E1001181(2010) [PubMed] [Europe PMC] [Abstract]
  6. "Defective regulation of microRNA target genes in myoblasts from facioscapulohumeral dystrophy patients."J. Biol. Chem. 288:34989-35002(2013) [PubMed] [Europe PMC] [Abstract]