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FLASH GENE
Symbol SULT2B1 contributors: mct - updated : 04-07-2017
HGNC name sulfotransferase family, cytosolic, 2B, member 1
HGNC id 11459
DNA
TYPE functioning gene
STRUCTURE 47.26 kb     6 Exon(s)
10 Kb 5' upstream gene genomic sequence study
regulatory sequence Promoter
cytosine-phosphate-guanine/HTF
Binding site
text structure
  • upstream of the coding region for SULT2B1b, GC-rich region
  • five Sp1 elements and Sp2 binding sites
  • MAPPING cloned Y linked N status confirmed
    RNA
    TRANSCRIPTS type messenger
    identificationnb exonstypebpproduct
    ProteinkDaAAspecific expressionYearPubmed
    6 splicing 1281 - 350 only in brain and testis 2013 24020383
  • SULT2B1a
  • avidly sulfonating pregnenolone but not cholesterol
  • exon 1A encodes for the unique amino-terminal end of SULT2B1a plus an additional 48 amino acids
  • 7 splicing 1228 - 365 . in platelets (stability in platelets is subject to regulation by the apoA-I component of HDL) . in epidermis granular layer coinciding with this being the area with the highest cholesterol sulfate content . selectively expressed in skin, mainly expressed in intestine and kidney 2013 24020383
  • SULT2B1b
  • alternative first exons: exon 1B encodes for only the unique amino-terminal region of SULT2B1b
  • preferentially sulfonating cholesterol
  • localized in the cytosol and/or nuclei
  • playing a role in regulating the responsiveness of cells to adrenal androgens via their direct inactivation or by preventing their conversion to more potent androgens and estrogens
  • EXPRESSION
    Type widely
       expressed in (based on citations)
    organ(s)
    SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
    Cardiovascularheart   highly
    Reproductivefemale systemplacenta  highly
     female systemovary   
     female systemuterus   
     male systemprostate  highly
    Respiratoryrespiratory tracttrachea  highly
    Skin/Tegumentskin   highly Homo sapiens
    tissue
    SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
    Epithelialbarrier liningepidermisstratum corneum  Homo sapiens
    Epithelialbarrier liningepidermisstratum granulosum  Homo sapiens
    cell lineage
    cell lines
    fluid/secretion
    at STAGE
    physiological period pregnancy
    Text highly, in placenta
    PROTEIN
    PHYSICAL PROPERTIES
    STRUCTURE
    motifs/domains
    the FSSKA sequence motif common to hydroxysteroid SULT family
    HOMOLOGY
    interspecies homolog to murine Sult2b1
    Homologene
    FAMILY sulfotransferase family
    CATEGORY enzyme
    SUBCELLULAR LOCALIZATION extracellular
        intracellular
    intracellular,cytoplasm,organelle,endoplasmic reticulum
    intracellular,cytoplasm,cytosolic
    intracellular,cytoplasm,cytoskeleton
    intracellular,nucleus
    text
  • colocalization with tubulin may indicate a connection of SULT2B1 to the cytoskeleton
  • basic FUNCTION
  • hydroxysteroid sulfotransferase, regulating the activity of adrenal androgens in tissues via their inactivation by sulfation
  • may be playing a regulatory role that protect against the mitogenic effects of androgens
  • catalyzes the sulfoconjugation of cholesterol to synthesize cholesterol sulfate (CS)
  • important role of SULT2B1 in the regulation of epidermal proliferation and differentiation and for constitution and maintenance of the barrier function in human skin
  • role of the sulfotransferase SULT2B1 in the regulation of the human epidermal cholesterol metabolism and thereby in the maintenance of a functional cutaneous permeability barrier
  • key role of SULT2B1 in homeostasis and barrier function of the human skin by providing cholesterol sulfate, an important regulator of the keratinocyte differentiation
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism hormone
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • may promote hepatocyte proliferation by inactivating oxysterol/NR1H3 signaling
  • leptin is a potential effector of SULT2B1 in improving metabolic function
  • cell & other
    REGULATION
    induced by estrogens
    inhibited by androgens
    ASSOCIATED DISORDERS
    corresponding disease(s) ARCI13
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
  • may serve as a novel prognostic biomarker for patients with colorectal carcinoma (CRC)
  • Therapy target
    SystemTypeDisorderPubmed
    cancerdigestivecolon
    therapeutic target for patients with colorectal carcinoma
    ANIMAL & CELL MODELS