Pl. Hartzell, COMPLEMENTATION OF SPORULATION AND MOTILITY DEFECTS IN A PROKARYOTE BY A EUKARYOTIC GTPASE, Proceedings of the National Academy of Sciences of the United Statesof America, 94(18), 1997, pp. 9881-9886
The complex prokaryote, Myxococcus xanthus, undergoes a program of mul
ticellular development when starved for nutrients, culminating in spor
ulation. M. xanthus makes MglA, a 22-kDa, soluble protein that is requ
ired for both multicellular development and gliding motility. MglA is
similar in sequence to the Saccharomyces cerevisiae SARI protein, a me
mber of the Ras/Rab/Rho superfamily of small eukaryotic GTPases. The S
RR1 gene, when integrated into the M. xanthus genome, complements the
sporulation defect of a Delta mglA strain. A forward, second-site muta
tion on the M. xanthus chromosome, rpm, in combination with SARI, rest
ores fruiting body morphogenesis and gliding motility to a Delta mglA
strain. The result that the rpm mutation suppresses the substitution o
f SAR1 for mglA suggests that Sar1p interacts with other M. xanthus pr
oteins to control the motility-dependent aggregation of cells during d
evelopment.