in mesophyll cell almost all glutamine synthetase is present in chloroplasts. In hair cells, glutamine synthetase is observed both in chloroplasts and in cytoplasm
in hair cells of plants grown under an Argon environment, regardless of the type of nitrogen source provided, only weak immunolabeling of enzyme is observed in the cytoplasm and in chloroplasts. In contrast, in hair cells of plants grown under N2, abundant immunolabeling of enzyme is observed in both sites
the N-terminal peptide acts as a transit peptide, targeting the protein to the plastids. The C-terminal extension peptide of plastid-located glutamine synthetase isozyme GS2a from Medicago truncatula is crucial for enzyme activity but needless for protein import into the plastids. The 16 amino acid C-terminal extension is present in all known plastid GS proteins
in mesophyll cell almost all glutamine synthetase is present in chloroplasts. In hair cells, glutamine synthetase is observed both in chloroplasts and in cytoplasm
in hair cells of plants grown under an Argon environment, regardless of the type of nitrogen source provided, only weak immunolabeling of enzyme is observed in the cytoplasm and in chloroplasts. In contrast, in hair cells of plants grown under N2, abundant immunolabeling of enzyme is observed in both sites
neural enzyme is retained in the cytoplasm. Two different glutamine synthetase transcripts are generated by tissue-specific alternative splicing. The liver transcript contains an alternative exon that is not present in the neural one
extracellular release is correlated with pathogenicity. The information to target the protein for export must be contained in its amino acid sequence and/or conformation
a much larger amount of GlnA1 is produced than is necessary for normal growth by the organism and a substantial proportion of this is found in the extracellular medium of cell cultures
a much larger amount of GlnA1 is produced than is necessary for normal growth by the organism and a substantial proportion of this is found in the extracellular medium of cell cultures
extracellular release is correlated with pathogenicity. The information to target the protein for export must be contained in its amino acid sequence and/or conformation
the N-terminus of glutamine synthetase, which constitutes a weak mitochondrial targeting signal, is sufficient to direct a chimeric protein to the mitochondria in hepatocytes and to the cytoplasm in astrocytes. The mitochondrial membrane potential in hepatocytes is more negative than in astrocytes
liver enzyme is targeted to mitochondria. Two different glutamine synthetase transcripts are generated by tissue-specific alternative splicing. The liver transcript contains an alternative exon that is not present in the neural one. This exon leads to acquisition of an upstream in-frame start codon and formation of a mitochondrial targeting signal