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Study of Mechanism of Proinsulin Gene Mutations in Diabetes Mellitus

  

  • Received:2014-01-20 Revised:2014-02-26 Published:2014-04-15 Online:2014-04-15

Abstract:    Abstract Objective: To construct several human proinsulin mutants related to diabetes and express in INS-1 cell. Methods: Human mild proinsulin gene as template ,use site-directed mutagenesis,generate four human proinsulin mutants by PCR,sequence each mutant,transfect four mutants、empty plasmid and mild plasmid into INS-1 cell by liposome 2000,determine insulin values in each cell solution by radioimmunoassay. Results: Proinsulin mutants are confirmed by sequence determination ,insulin values in culture solution of H-C(B19)G、 H-L(B11)P、H-R(S6)C mutants are less than that of wild type and found no significant differences statistically with empty plasmid. insulin values of H-F(B25)L is more than that of empty plasmid and the former three mutants. Conclusions: Successfully construct and express four human proinsulin mutants, different mutants result in diabetes through different mechanism.

Key words:  Endoplastic reticulum stress, Proinsulin misfolding, mutagenesis, site-directed, plasmids, permanent neonatal diabetes mellitus, transfection, B细胞功能衰竭