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FLASH GENE
Symbol PURA contributors: mct - updated : 28-09-2013
HGNC name purine-rich element binding protein A
HGNC id 9701
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
1 - 5304 34.8 322 - 2003 12972605
EXPRESSION
Type ubiquitous
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Lymphoid/Immunespleen    
Reproductivefemale systemovary   
 male systemprostate   
Urinarykidney    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Lymphoid    
cells
SystemCellPubmedSpeciesStageRna symbol
Nervousneuron
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period fetal
Text eye
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • an N-terminal glycine-rich region
  • three repeats of a 23-amino acid class I motif
  • two repeats of a 26-amino acid class II motif
  • an amphipathic helix
  • a C-terminal glutamine-glutamate-rich domain
  • conjugated PhosphoP
    mono polymer homomer , heteromer , dimer , trimer
    HOMOLOGY
    interspecies homolog to murine Pura (99.7 pc)
    homolog to rattus Pura (99.7 pc)
    intraspecies homolog to PURB
    Homologene
    FAMILY
  • PUR DNA-binding protein family
  • CATEGORY regulatory , DNA associated , transcription factor
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,cytosolic,ribosome
    intracellular,nucleus
    text associated with polyribosomes
    basic FUNCTION
  • may be play a role in the initiation of DNA replication and in recombination
  • involved in targeting mRNPs to polyribosomes in cooperation with other RNA-binding proteins
  • acting as a probable transcription activator
  • PURalpha and PURbeta repressed alpha-myosin heavy chain (alpha-MHC) gene expression in the presence of upstream regulatory sequences of the gene
  • participate in transcriptional as well as translational regulation of alpha-MHC expression in cardiac myocytes
  • PURA, and PURB, collaborate with Sp3 to regulate a transcriptional program that enables muscle cells to remodel their phenotype
  • structurally related single-stranded DNA/RNA-binding proteins implicated in the control of cell growth and differentiation
  • Pur alpha and Pur beta repress smooth muscle alpha-actin gene transcription by means of DNA strand-selective cis-element binding and cell type-dependent protein-protein interactions
  • involved in many aspects of nucleic acid homeostasis including the regulation of DNA replication, DNA repair, gene transcription, RNA transport, and mRNA translation
  • has a role in nucleotide excision repair and the repair of UVC-induced DNA damage
  • plays an important role in a variety of cellular processes including transcriptional regulation, cell proliferation and oncogenic transformation
  • potential role in the regulation of the expression and cellular distribution of dendritic and axonal protein
  • importance in the proliferation of neuronal precursor cells during postnatal brain development, suggesting a role in the regulation of the expression and cellular distribution of dendritic and axonal proteins
  • DNA-binding protein with high affinity for the single-stranded PUR-motif (GGN)n
  • critical for myeloid cell development, muscle development, and brain development, including trafficking of mRNA to neuronal dendrites
  • CELLULAR PROCESS cell life, proliferation/growth
    nucleotide, replication
    nucleotide, transcription, regulation
    PHYSIOLOGICAL PROCESS development
    text
  • nervous system development
  • positive regulation of cell proliferation
  • PATHWAY
    metabolism
    signaling
    a component
  • heterodimer with PURB
  • heterotrimer with PURB and YBX1/Y-box protein 1
  • INTERACTION
    DNA specifically binding to the purine-rich single strand of the PUR element located upstream of the MYC gene
    RNA
    small molecule
    protein
  • interacting with CDK2
  • binding to E2F1
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) DEL5Q31.3 , MRD31
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    tumoral   deletion    
    in myelodysplastic syndrome, acute myelogenous leukemia
    constitutional        
    leads to a prolongation of neuronal precursor cell proliferation during postnatal development, a reduced expression of MAP2 and pathological hyperphosphorylation of axonal proteins
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    cancerreproductiveprostate
    for hormone-refractory prostate cancer
    ANIMAL & CELL MODELS
  • PURA(-/-) mice
  • Pur&
  • 945;(-/-) mice displayed a megalencephaly and histopathological findings including axonal swellings and hyperphosphorylation of neurofilaments