The objective of this study was to examine the distribution of rDNA loci in
the genus Glycine Willd. by fluorescent in situ hybridization (FISH) using
the internal transcribed spacer (ITS) region of nuclear ribosomal DNA as a
probe. The hybridized rDNA probe produced two distinct yellow signals on r
eddish chromosomes representing two NORs in 16 diploid (2n=40) species. Ane
udiploid (2n=38) and aneutetraploid (2n=78) Glycine tomentella Hayata also
exhibited two rDNA sites. However, the probe hybridized with four chromosom
es as evidenced by four signals in two diploid species (Glycine curvata Tin
d. and Glycine cyrtoloba Tind.) and tetraploid (2n=80) G. tabacina (Labill.
) Benth. and G. tomentella. Synthesized amphiploids (2n=80) of Glycine cane
scens F. J. Herm. (2n=40) and the 40-chromosome G. tomentella also showed f
our signals. This study demonstrates that the distribution of the rDNA gene
in the 16 Glycine species studied is highly conserved and that silence of
the rDNA locus may be attributed to amphiplasty during diploidization and s
peciation.