R. Dammann et al., CHROMATIN STRUCTURES AND TRANSCRIPTION OF RDNA IN YEAST SACCHAROMYCES-CEREVISIAE, Nucleic acids research, 21(10), 1993, pp. 2331-2338
The chromatin structure of yeast ribosomal DNA was analyzed in vivo by
crosslinking intact cells with psoralen. We found that in exponential
ly growing cultures the regions coding for the 35S rRNA precursor fall
into two distinct classes. One class was highly accessible to psorale
n and associated with nascent RNAs, characteristic for transcriptional
ly active rRNA genes devoid of nucleosomes, whereas the other class sh
owed a crosslinking pattern indistinguishable from that of bulk chroma
tin and was interpreted to represent the inactive rRNA gene copies. By
crosslinking the same strain growing in complex or minimal medium, we
have shown that yeast cells can modulate the proportion of active (no
n-nucleosomal) and inactive (nucleosomal) rRNA gene copies in response
to variations in environmental conditions which suggests that yeast c
an regulate rRNA synthesis by varying the number of active gene copies
, in contrast to the vertebrate cells studied so far. Whereas intergen
ic spacers flanking inactive rRNA gene copies are packaged in a regula
r nucleosomal array, spacers flanking active genes show an unusual cro
sslinking pattern suggesting a complex interaction of regulatory tacto
rs and histones with DNA.