Telomeric restriction fragments were genetically mapped to a previousl
y described linkage map of Magnaporthe grisea, using RFLPs identified
by a synthetic probe, (TTAGGG)(3). Frequent rearrangement of telomeric
sequences was observed in progeny isolates creating a potential for m
isinterpretation of data. Therefore a consensus segregation data set w
as used to minimize mapping errors. Twelve of the 14 telomeres were fo
und to be genetically linked to existing RFLP markers. Second-dimensio
nal electrophoresis of restricted chromosomes confirmed these linkage
assignments and revealed the chromosomal location of the two unlinked
telomeres. We were thus able to assign all 14 M. grisea telomeres to t
heir respective chromosome ends. The Achilles' cleavage (AC) technique
was employed to determine that chromosome 1 markers II and CH5-120H w
ere similar to 1.8 Mb and 1.28 Mb, respectively, from their nearest te
lomeres. RecA-AC was also used to determine that unlinked telomere 6 w
as similar to 530 kb from marker CH5-176H in strain 2539 and 580 kb in
Guy11. These experiments indicated that large portions of some chromo
some ends are unrepresented by genetic markers and provided estimates
of the relationship of genetic to physical distance in these regions o
f the genome.