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Cloning and characterization of a second lamprey pituitary glycoprotein hormone, thyrostimulin (GpA2/GpB5).

Gen. Comp. Endocrinol.. 2018-01; 
HauskenKrist N,TizonBelen,ShpilmanMichal,BartonShannon,DecaturWayne,PlachetzkiDavid,KavanaughScott,Ul-HasanSabah,Levavi-SivanBerta,SowerStac
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Catalog Antibody … Louis, MO) and either rabbit-anti-His (Genscript, Piscataway, NJ), rabbit-anti-lGpB5 (Cocalico, Stevens, PA), or rabbit-anti-lGpA2 (Cocalico) in 3% BSA/TBST [1:4000]) were applied for 1 h. Biotin conjugated goat-anti-rabbit IgG (1:20,000; Thermo Fisher, Waltham, MA … Get A Quote

摘要

A novel heterodimeric glycoprotein hormone (GpH) comprised of alpha (GpA2) and beta (GpB5) subunits was discovered in 2002 and called thyrostimulin for its ability to activate the TSH receptor in mammals, but its central function in vertebrates has not been firmly established. We report here the cloning and expression of lamprey (l)GpB5, and its ability to heterodimerize with lGpA2 to form a functional l-thyrostimulin. The full-length cDNA of lGpB5 encodes 174 amino acids with ten conserved cysteine residues and one glycosylation site that is conserved with other vertebrate GpB5 sequences. Phylogenetic and synteny analyses support that lGpB5 belongs to the vertebrate GpB5 clade. Heterodimerization of lGpB5 ... More

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