APPROACHES TO THE MOLECULAR-CLONING OF PROTEIN-TYROSINE PHOSPHATASES IN INSULIN-SENSITIVE TISSUES

被引:0
作者
GOLDSTEIN, BJ
ZHANG, WR
HASHIMOTO, N
KAHN, CR
机构
[1] JOSLIN DIABET CTR, DIV RES, 1 JOSLIN PL, BOSTON, MA 02215 USA
[2] HARVARD UNIV, BRIGHAM & WOMENS HOSP, SCH MED, DEPT MED, BOSTON, MA 02115 USA
关键词
INSULIN ACTION; PROTEIN-TYROSINE PHOSPHATASES; INSULIN RESISTANCE; PROTEIN PHOSPHORYLATION; INSULIN RECEPTOR;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The intrinsic tyrosyl kinase activity of the insulin receptor is regulated by a balance between insulin-induced receptor autophosphorylation, which stimulates the receptor kinase, and enzymatic dephosphorylation of the receptor, which deactivates its kinase activity. The cellular protein-tyrosine phosphatase (PTPase) enzymes responsible for reversing the activated state of the insulin receptor have not been characterized. Our laboratory is interested in identifying and cloning the specific PTPase(s) that regulate the phosphorylation state of the insulin receptor. This chapter will summarize the design and results of our initial molecular cloning studies to identify specific PTPases in insulin-sensitive tissues that may have a potential physiological role in insulin action and clinical insulin resistance.
引用
收藏
页码:107 / 113
页数:7
相关论文
共 33 条
[1]   HUMAN-PLACENTA PROTEIN-TYROSINE-PHOSPHATASE - AMINO-ACID SEQUENCE AND RELATIONSHIP TO A FAMILY OF RECEPTOR-LIKE PROTEINS [J].
CHARBONNEAU, H ;
TONKS, NK ;
KUMAR, S ;
DILTZ, CD ;
HARRYLOCK, M ;
COOL, DE ;
KREBS, EG ;
FISCHER, EH ;
WALSH, KA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5252-5256
[2]   CLONING OF A CDNA FOR A MAJOR HUMAN PROTEIN-TYROSINE-PHOSPHATASE [J].
CHERNOFF, J ;
SCHIEVELLA, AR ;
JOST, CA ;
ERIKSON, RL ;
NEEL, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) :2735-2739
[3]   MICROINJECTION OF A PROTEIN-TYROSINE-PHOSPHATASE INHIBITS INSULIN ACTION IN XENOPUS OOCYTES [J].
CICIRELLI, MF ;
TONKS, NK ;
DILTZ, CD ;
WEIEL, JE ;
FISCHER, EH ;
KREBS, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5514-5518
[4]   CDNA ISOLATED FROM A HUMAN T-CELL LIBRARY ENCODES A MEMBER OF THE PROTEIN-TYROSINE-PHOSPHATASE FAMILY [J].
COOL, DE ;
TONKS, NK ;
CHARBONNEAU, H ;
WALSH, KA ;
FISCHER, EH ;
KREBS, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5257-5261
[5]   EXPRESSION OF A HUMAN T-CELL PROTEIN-TYROSINE-PHOSPHATASE IN BABY HAMSTER-KIDNEY CELLS [J].
COOL, DE ;
TONKS, NK ;
CHARBONNEAU, H ;
FISCHER, EH ;
KREBS, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (18) :7280-7284
[6]   THE TRIUMVIRATE - BETA-CELL, MUSCLE, LIVER - A COLLUSION RESPONSIBLE FOR NIDDM [J].
DEFRONZO, RA .
DIABETES, 1988, 37 (06) :667-687
[7]  
FLORESRIVEROS JR, 1989, J BIOL CHEM, V264, P21557
[8]   THE RAT INSULIN-RECEPTOR - PRIMARY STRUCTURE AND CONSERVATION OF TISSUE-SPECIFIC ALTERNATIVE MESSENGER-RNA SPLICING [J].
GOLDSTEIN, BJ ;
DUDLEY, AL .
MOLECULAR ENDOCRINOLOGY, 1990, 4 (02) :235-244
[9]  
GOLDSTEIN BJ, 1991, ADV PROTEIN PHOSPHAT, V6, P1
[10]   CLONING AND EXPRESSION OF A PROTEIN-TYROSINE-PHOSPHATASE [J].
GUAN, KL ;
HAUN, RS ;
WATSON, SJ ;
GEAHLEN, RL ;
DIXON, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1501-1505