Open AccessGlutamine synthetase expression in perinatal spiny mouse liver
Author(s) -
Lamers Wouter H.,
Boon Louis,
van Hemert Formijn J.,
Labruyère Wil T.,
de Jong Petra,
Ruijter Jan M.,
Moorman Antoon F. M.
Publication year - 1999
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1046/j.1432-1327.1999.00436.x
Subject(s) - glutamine synthetase , biology , messenger rna , polysome , translational efficiency , medicine , gene expression , protein biosynthesis , endocrinology , microbiology and biotechnology , translation (biology) , biochemistry , glutamine , rna , gene , ribosome , amino acid
The pronounced increase in the protein/mRNA ratio of ammonia‐metabolising enzymes in rat liver in the last prenatal week represents a clear example of a post‐transcriptional level of control of gene expression. Both the underlying mechanism, namely an increase in translational efficiency of the mRNA and/or enhanced stability of the protein, and its importance for perinatal adaptation are unknown. We investigated this process in spiny mouse liver, because the comparison of rat and spiny mouse can discriminate adaptively from developmentally regulated processes in the perinatal period. We focused on glutamine synthetase (GS) because of the conveniently small size of its mRNA. Prenatally, GS enzyme activity slowly accumulated to ≈1.3 U·g −1 liver at birth and postnatally more rapidly to 5.5 U·g −1 at 2 weeks. Both phases of enzyme accumulation obeyed exponential functions. Western‐blot analysis showed that changes in GS activity reflected changes in GS protein content. GS mRNA content of the liver was 45 fmol·g −1 at 2 weeks before birth and slowly declined to ≈ 25 fmol·g −1 at 2 weeks after birth. The GS protein/mRNA ratio increased 2.5‐fold prenatally and sixfold postnatally. Analysis of prenatal and postnatal polysome profiles revealed no evidence of GS mRNA‐containing ribonucleoprotein particles. Instead, GS mRNAs were (fully) occupied by 12 ribosomes, indicating regulation at the level of elongation. The kinetics of GS protein accumulation, in conjunction with GS mRNA content, are consistent with an ≈ sixfold increase in its rate of synthesis at birth as the result of a corresponding stimulation of the rate of elongation.