C. Kawamura et al., THE MELANIN BIOSYNTHESIS GENES OF ALTERNARIA-ALTERNATA CAN RESTORE PATHOGENICITY OF THE MELANIN-DEFICIENT MUTANTS OF MAGNAPORTHE-GRISEA, Molecular plant-microbe interactions, 10(4), 1997, pp. 446-453
The phytopathogenic fungi Magnaporthe grisea and Alternaria alternata
produce melanin via the polyketide biosynthesis, and both fungi form m
elanized colonies. However the site of melanin deposition and the role
of melanin in pathogenicity differ between these two fungi. M. grisea
accumulates melanin in appressoria, and their melanization is essenti
al for host penetration. On the other hand, A. alternata produces colo
rless appressoria, and melanin is not relevant to host penetration. We
examined whether the melanin biosynthesis genes of A. alternata could
complement the melanin-deficient mutations of A. grisea. Melanin-defi
cient, nonpathogenic mutants of M. grisea, albino (Alb(-)), rosy (Rsy(
-)), and buff (Buf(-)), were successfully transformed with a cosmid cl
one pMBR1 that carries melanin biosynthesis genes ALM, BRM1, and BRM2
of A. alternata. This transformation restored the melanin synthesis of
the Alb(-) and Buf(-) mutants, but not that of the Rsy(-) mutant. The
melanin-restored transformants regained mycelial melanization, appres
sorium melanization, and pathogenicity to rice. Further, transformatio
n of Alb(-) and Buf(-) mutants with subcloned ALM and BRM2 genes, resp
ectively, also produced melanin-restored transformants. These results
indicate that the Alternaria genes ALM and BRM2 can restore pathogenic
ity to the mutants Alb(-) and Buf(-), respectively, due to their funct
ion during appressorium development in M. grisea.