TY - JOUR
T1 - Ribosomal RNA genes of Drosophila melanogaster have a novel chromatin structure
AU - Udvardy, Andor
AU - Louis, Christos
AU - Han, Stella
AU - Schedl, Paul
N1 - Funding Information:
We thank K. Udvardy for excellent technical assistance. We would especially like to acknowledge Dr Abe Worcel for his extensive assistance and advice during the course of this work. and for stimulating discussions. Support was provided by research grants from XIH, ACS and R’SF. P.S. also t,hanks the March of Dimes Birth Defect Foundation for funds from the Basil O’Conner Starter Grant Pro,gram. and a research grant.
PY - 1984/5/15
Y1 - 1984/5/15
N2 - We have examined the chromatin organization of the Drosophila melanogaster ribosomal RNA genes using both micrococcal nuclease and DNase I. Several findings are of interest. First, the transcribed DNA segments of the rRNA repeat unit appear to be packaged into an unstable or "multiphasic" nucleosome structure. Second, the 5′ end of the transcription unit is preferentially exposed to nuclease attack. Third, the non-transcribed spacer immediately upstream from the transcription start site has a novel chromatin organization with micrococcal nuclease and DNase I cleavage sites spaced at intervals of about 240 base-pairs. This unusual fragment distribution appears to reflect the underlying sequence organization of the spacer DNA segment, which consists of a series of tandemly repeated 239 base-pair sequence blocks. We have also examined the chromatin structure of the rRNA repeat unit after extraction of nuclei with different concentrations of salt. Our results suggest that the higher order structures may be of importance in determining the novel chromatin organization of the rRNA repeat unit.
AB - We have examined the chromatin organization of the Drosophila melanogaster ribosomal RNA genes using both micrococcal nuclease and DNase I. Several findings are of interest. First, the transcribed DNA segments of the rRNA repeat unit appear to be packaged into an unstable or "multiphasic" nucleosome structure. Second, the 5′ end of the transcription unit is preferentially exposed to nuclease attack. Third, the non-transcribed spacer immediately upstream from the transcription start site has a novel chromatin organization with micrococcal nuclease and DNase I cleavage sites spaced at intervals of about 240 base-pairs. This unusual fragment distribution appears to reflect the underlying sequence organization of the spacer DNA segment, which consists of a series of tandemly repeated 239 base-pair sequence blocks. We have also examined the chromatin structure of the rRNA repeat unit after extraction of nuclei with different concentrations of salt. Our results suggest that the higher order structures may be of importance in determining the novel chromatin organization of the rRNA repeat unit.
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U2 - 10.1016/0022-2836(84)90470-4
DO - 10.1016/0022-2836(84)90470-4
M3 - Article
C2 - 6233426
AN - SCOPUS:0021717365
SN - 0022-2836
VL - 175
SP - 113
EP - 130
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 2
ER -