“…The main regulator, Ph1, was discovered 50 years ago (Riley and Chapman, 1958;Sears and Okamoto, 1958) and only recently characterized at the molecular level (Griffiths et al, 2006;Al-Kaff et al, 2007). However, the very peculiar nature of the Ph1 locus, which consists of a cluster of cyclin-dependant kinases (cdk-like genes) and a segment of subtelomeric heterochromatin, does not readily explain the multiple cytological effects attributed to Ph1 (Feldman, 1993;Mikhailova et al, 1998;Martinez-Perez et al, 2003;Prieto et al, 2005;Corredor et al, 2007). On the other hand, Ph2, another suppressor of homoeologous associations (Upadhya and Swaminathan, 1967;MelloSampayo, 1971), was shown to affect synaptic progression (Martinez et al, 2001) but the genes responsible for the phenotype are still to be identified (Sutton et al, 2003).…”