Identification of a 100-kDa phosphoprotein in developing murine embryos as elongation factor 2

Thomas L. Brown, Wendy C. Fischer, Michael D. Collins, Barun K De, William J. Scott

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Protein phosphorylation is a key regulatory mechanism for several functions. Although the complex control of organogenesis and growth most likely includes such mechanisms, few reports have examined protein phosphorylation in the developing mammal. The identification and characterization of mammalian embryonic phosphoproteins will allow a greater understanding of the regulation and mechanisms of developmental processes. Phosphorylation of the endogenous mouse proteins during development revealed a 100-kDa protein, located in the cytosolic fraction, to be the major substrate. The Ca2+-calmodulin kinase inhibitors, trifluoperazine and ethylene glycol bis(β-aminoethyl ether)N, N′-tetraacetic acid, inhibited this phosphorylation. Inhibitors of protein kinase C (H-7)- and cAMP-dependent protein kinase, as well as the tyrosine kinase inhibitor, genistein, had no effect. One- and two-dimensional phosphoamino acid analysis indicated that phosphothreonine was the major phosphorylated amino acid. To determine the identity of this protein, the 100-kDa band was isolated and submitted for amino acid analysis and N-terminal sequencing. The N-terminal sequence Val-Asn-Phe-Thr-Val-Asp-Gln-Ile-Arg-Ala-Ile-Met-Asp-Lys, was identical to the N-terminal sequence of human, hamster and rat elongation factor 2 (EF-2). Western blotting analysis confirmed that the 100 kDa protein was EF-2. Our results of phosphorylated EF-2 in the developing mouse are in agreement with those reported in the avian embryo. However, our results differ in that phosphotyrosine detected in avian embryos could not be detected in murine embryos. This is the first report to demonstrate EF-2 in the developing mammalian embryo and its specific phosphorylation pattern. Our data suggest that the functional phosphoregulation of elongation factor 2 during protein synthesis in mammals is conserved from the developing embryo to the adult and thus emphasizes the importance of EF-2 in normal development and survival.

Original languageEnglish (US)
Pages (from-to)105-110
Number of pages6
JournalArchives of Biochemistry and Biophysics
Volume309
Issue number1
DOIs
StatePublished - Jan 1 1994
Externally publishedYes

Fingerprint

Peptide Elongation Factor 2
Phosphoproteins
Phosphorylation
Embryonic Structures
Proteins
Mammals
Phosphothreonine
Phosphoamino Acids
Mammalian Embryo
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
Amino Acids
Trifluoperazine
Calcium-Calmodulin-Dependent Protein Kinases
Phosphotyrosine
Organogenesis
Ethylene Glycol
Genistein
Cyclic AMP-Dependent Protein Kinases
Cricetinae
Ether

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

Cite this

Identification of a 100-kDa phosphoprotein in developing murine embryos as elongation factor 2. / Brown, Thomas L.; Fischer, Wendy C.; Collins, Michael D.; De, Barun K; Scott, William J.

In: Archives of Biochemistry and Biophysics, Vol. 309, No. 1, 01.01.1994, p. 105-110.

Research output: Contribution to journalArticle

Brown, Thomas L. ; Fischer, Wendy C. ; Collins, Michael D. ; De, Barun K ; Scott, William J. / Identification of a 100-kDa phosphoprotein in developing murine embryos as elongation factor 2. In: Archives of Biochemistry and Biophysics. 1994 ; Vol. 309, No. 1. pp. 105-110.
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