Literature DB >> 3261169

Degradation of inositol 1,3,4,5-tetrakisphosphates by porcine brain cytosol yields inositol 1,3,4-trisphosphate and inositol 1,4,5-trisphosphate.

D Höer1, A Kwiatkowski, C Seib, W Rosenthal, G Schultz, E Oberdisse.   

Abstract

Inositol 1,3,4,5-tetrakisphosphates (Ins(1,3,4,5)P4), 32P-labelled in positions 4 and 5 were prepared enzymatically, using [4-32P]-phosphatidylinositol 4-phosphate (PtdInsP) and [5-32P]phosphatidylinositol 4,5-bisphosphate (PtdInsP2) as substrates, respectively. Degradation studies of Ins(1,3,4,5)P4, using an enriched phosphatase preparation from porcine brain cytosol, led to the formation of two inositol trisphosphate isomers which were identified as inositol 1,3,4-trisphosphate (Ins(1,3,4)P3) and inositol 1,4,5-trisphosphate (Ins(1,4,5)P3). This novel degradation pathway of Ins(1,3,4,5)P4 to Ins(1,4,5)P3 provides an additional source for the generation of Ins(1,4,5)P3, involving a 3-phosphatase.

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Year:  1988        PMID: 3261169     DOI: 10.1016/0006-291x(88)90191-x

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  13 in total

1.  D-myo-inositol 1,3,4,5-tetrakisphosphate releases Ca2+ from crude microsomes and enriched vesicular plasma membranes, but not from intracellular stores of permeabilized T-lymphocytes and monocytes.

Authors:  A H Guse; E Roth; F Emmrich
Journal:  Biochem J       Date:  1992-12-01       Impact factor: 3.857

Review 2.  Metabolism of the inositol phosphates produced upon receptor activation.

Authors:  S B Shears
Journal:  Biochem J       Date:  1989-06-01       Impact factor: 3.857

3.  Inositol 1,3,4,5-tetrakisphosphate causes release of Ca2+ from permeabilized mouse lymphoma L1210 cells by its conversion into inositol 1,4,5-trisphosphate.

Authors:  P J Cullen; R F Irvine; B K Drøbak; A P Dawson
Journal:  Biochem J       Date:  1989-05-01       Impact factor: 3.857

4.  A simple enzymic method to separate [3H]inositol 1,4,5- and 1,3,4-trisphosphate isomers in tissue extracts.

Authors:  E D Kennedy; I H Batty; E R Chilvers; S R Nahorski
Journal:  Biochem J       Date:  1989-05-15       Impact factor: 3.857

5.  Synergistic control of Ca2+ mobilization in permeabilized mouse L1210 lymphoma cells by inositol 2,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate.

Authors:  P J Cullen; R F Irvine; A P Dawson
Journal:  Biochem J       Date:  1990-10-15       Impact factor: 3.857

6.  Properties of a soluble inositol 1,3,4,5-tetrakisphosphate 3-phosphatase from porcine brain.

Authors:  A Höer; D Höer; E Oberdisse
Journal:  Biochem J       Date:  1990-09-15       Impact factor: 3.857

7.  Metabolism of the biologically active inositol phosphates Ins(1,4,5)P3 and Ins(1,3,4,5)P4 by ovarian follicles of Xenopus laevis.

Authors:  R P McIntosh; J E McIntosh
Journal:  Biochem J       Date:  1990-05-15       Impact factor: 3.857

8.  Rat liver contains a potent endogenous inhibitor of inositol 1,3,4,5-tetrakisphosphate 3-phosphatase.

Authors:  M E Hodgson; S B Shears
Journal:  Biochem J       Date:  1990-05-01       Impact factor: 3.857

9.  In Dictyostelium discoideum inositol 1,3,4,5-tetrakisphosphate is dephosphorylated by a 3-phosphatase and a 1-phosphatase.

Authors:  P Van Dijken; A A Lammers; P J Van Haastert
Journal:  Biochem J       Date:  1995-05-15       Impact factor: 3.857

10.  Inositol 1,3,4,5,6-pentakisphosphate and inositol hexakisphosphate are inhibitors of the soluble inositol 1,3,4,5-tetrakisphosphate 3-phosphatase and the inositol 1,4,5-trisphosphate/1,3,4,5-tetrakisphosphate 5-phosphatase from pig brain.

Authors:  A Höer; E Oberdisse
Journal:  Biochem J       Date:  1991-08-15       Impact factor: 3.857

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