Molecular Biology and Evolution, Vol 12, 189-197, Copyright © 1995 by Society for Molecular Biology and Evolution
G Pesole, C Gissi, C Lanave and C Saccone
The evolution of the prokaryotic glutamine synthase (GS) genes, namely the
GSI and GSII isoforms, has been investigated using the second codon
positions, which have previously proven to behave as a good molecular
clock. Our data confirm the early divergence between prokaryotic and
eukaryotic GSII before the splitting between plants and animals. The
phylogenetic tree of the GSI isoforms shows Archaebacteria to be more
closely related to Eubacteria than to Eukaryotes. This finding is confirmed
by the phylogenetic analysis carried out on both large and small subunits
of rRNA. However, differently from the rRNA analyses, Crenarchaeota and
Euryarchaeota Archaebacteria, as well as high- and low-GC gram-positive
bacteria, appear to be polyphyletic. We provide evidence that the observed
polyphyly of Archaebacteria might be only apparent, resulting from a gene
duplication event preceding the split between Archaebacteria and Eubacteria
and followed by the retention of only one isoform in the extant lineages.
Both gram-negative bacteria and high-GC gram-positive bacteria, which
appear closely related, have GS activity regulated by an
adenylylation/deadenylylation mechanism. A lateral gene transfer from
Archaebacteria to low-GC eubacteria is invoked to explain the observed
polyphyly of gram-positive bacteria.
ORIGINAL ARTICLE
Glutamine synthetase gene evolution in bacteria
Dipartimento di Biochimica e Biologia Molecolare, Universita di Bari, Italy.
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