C. Caggese et al., GENETIC, MOLECULAR AND DEVELOPMENTAL ANALYSIS OF THE GLUTAMINE-SYNTHETASE ISOZYMES OF DROSOPHILA-MELANOGASTER, Genetica, 94(2-3), 1994, pp. 275-281
The glutamine synthetase isozymes of Drosophila melanogaster offer an
attractive model for the study of the molecular genetics and evolution
of a small gene family encoding enzymatic isoforms that evolved to as
sume a variety of specific and sometimes essential biological function
s. In Drosophila melanogaster two GS isozymes have been described whic
h exhibit different cellular localisation and are coded by a two-membe
r gene family. The mitochondrial GS structural gene resides at the 21B
region of the second chromosome, the structural gene for the cytosoli
c isoform at the 10B region of the X chromosome. cDNA clones correspon
ding to the two genes have been isolated and sequenced. Evolutionary a
nalysis data are in accord with the hypothesis that the two Drosophila
glutamine synthetase genes are derived from a duplication event that
occurred near the time of divergence between Insecta and Vertebrata. B
oth isoforms catalyse all reactions catalysed by other glutamine synth
etases, but the different kinetic parameters and the different cellula
r compartmentalisation suggest strong functional specialisation. In fa
ct, mutations of the mitochondrial GS gene produce embryo-lethal femal
e sterility, defining a function of the gene product essential for the
early stages of embryonic development. Preliminary results show strik
ingly distinct spatial and temporal patterns of expression of the two
isoforms at later stages of development.