Fernandez R, Tabarini D, Frasch M, Azpiazu N, Schlessinger J (1995)
Publication Status: Published
Publication Type: Journal article, Original article
Publication year: 1995
Publisher: OXFORD UNIV PRESS UNITED KINGDOM
Book Volume: 14
Pages Range: 3373-3384
Journal Issue: 14
We report the cloning and primary structure of the Drosophila insulin receptor gene (inr), functional expression of the predicted polypeptide, and the isolation of mutations in the inr locus, Our data indicate that the structure and processing of the Drosophila insulin proreceptor are somewhat different from those of the mammalian insulin and IGF 1 receptor precursors. The INR proreceptor (M(r) 280 kDa) is processed proteolytically to generate an insulin-binding alpha subunit (M(r) 120 kDa) and a beta subunit (M(r) 170 kDa) with protein tyrosine kinase domain, The INR beta(170) subunit contains a novel domain at the carboxyterminal side of the tyrosine kinase, in the form of a 60 kDa extension which contains multiple potential tyrosine autophosphorylation sites, This 60 kDa G-terminal domain undergoes cell-specific proteolytic cleavage which leads to the generation of a total of four polypeptides (alpha(120), beta(170), beta(90) and a free 60 kDa C-terminus) from the inr gene. These subunits assemble into mature INR receptors with the structures alpha(2)(beta(170))(2) or alpha(2)(beta(90))(2). Mammalian insulin stimulates tyrosine phosphorylation of both types of beta subunits, which in turn allows the beta(170), but not the beta(90) subunit, to bind directly to p85 SH2 domains of PI-3 kinase, It is likely that the two different isoforms of INR have different signaling potentials, Finally, we show that loss of function mutations in the inr gene, induced by either a P-element insertion occurring within the predicted ORF, or by ethylmethane sulfonate treatment, render pleiotropic recessive phenotypes that lead to embryonic lethality, The activity of inr appears to be required in the embryonic epidermis and nervous system among others, since development of the cuticle, as well as the peripheral and central nervous systems are affected by inr mutations.
APA:
Fernandez, R., Tabarini, D., Frasch, M., Azpiazu, N., & Schlessinger, J. (1995). THE DROSOPHILA INSULIN-RECEPTOR HOMOLOG - A GENE ESSENTIAL FOR EMBRYONIC-DEVELOPMENT ENCODES 2 RECEPTOR ISOFORMS WITH DIFFERENT SIGNALING POTENTIAL. EMBO Journal, 14(14), 3373-3384.
MLA:
Fernandez, R, et al. "THE DROSOPHILA INSULIN-RECEPTOR HOMOLOG - A GENE ESSENTIAL FOR EMBRYONIC-DEVELOPMENT ENCODES 2 RECEPTOR ISOFORMS WITH DIFFERENT SIGNALING POTENTIAL." EMBO Journal 14.14 (1995): 3373-3384.
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