TY - JOUR
T1 - Variegated chromatin structures of mouse ribosomal RNA genes
AU - Davis, Alan H.
AU - Reudelhuber, Timothy L.
AU - Garrard, William T.
AU - Chambon, P.
N1 - Funding Information:
We are grateful to Drs N. Arnheim, I. Grummt, N. Hastie, M. Muramatsu and J. Reilly for their generous gifts of recombinant plasmids. We thank our colleagues, Drs D. Ball, D. Gross and S. Rose for a critical review of this manuscript. We are indebted to Ms Marie Rotondi for typing this manuscript. This research was supported by grants from the National Institutes of Health and The Robert A. Welch Foundation.
PY - 1983/6/15
Y1 - 1983/6/15
N2 - We have employed a chromatin fractionation procedure on micrococcal nuclease-digested nuclei to examine the chromatin structure of mouse ribosomal RNA genes in two systems that differ by at least 14-fold in the level of ribosomal RNA transcription. In a cultured cell line enriched in transcriptionally active ribosomal chromatin, most ribosomal sequences are preferentially sensitive to digestion by micrococcal nuclease, reside in an insoluble chromatin fraction, and lack typical nucleosomal packaging; only minor amounts of ribosomal sequences are packaged into soluble, nucleosomal chromatin. By contrast, in adult liver, which is enriched in transcriptionally inactive ribosomal chromatin, the majority of ribosomal genes are packaged into soluble, nucleosomal chromatin. However, a significant fraction of liver ribosomal chromatin is insoluble and possesses a non-nucleosomal structure. Therefore, within a single cell population or tissue, mouse ribomal RNA genes are organized into both nucleosomal and non-nucleosomal chromatin structures. We suggest that these structures have functional significance.
AB - We have employed a chromatin fractionation procedure on micrococcal nuclease-digested nuclei to examine the chromatin structure of mouse ribosomal RNA genes in two systems that differ by at least 14-fold in the level of ribosomal RNA transcription. In a cultured cell line enriched in transcriptionally active ribosomal chromatin, most ribosomal sequences are preferentially sensitive to digestion by micrococcal nuclease, reside in an insoluble chromatin fraction, and lack typical nucleosomal packaging; only minor amounts of ribosomal sequences are packaged into soluble, nucleosomal chromatin. By contrast, in adult liver, which is enriched in transcriptionally inactive ribosomal chromatin, the majority of ribosomal genes are packaged into soluble, nucleosomal chromatin. However, a significant fraction of liver ribosomal chromatin is insoluble and possesses a non-nucleosomal structure. Therefore, within a single cell population or tissue, mouse ribomal RNA genes are organized into both nucleosomal and non-nucleosomal chromatin structures. We suggest that these structures have functional significance.
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U2 - 10.1016/S0022-2836(83)80038-2
DO - 10.1016/S0022-2836(83)80038-2
M3 - Article
C2 - 6864798
AN - SCOPUS:0020642906
SN - 0022-2836
VL - 167
SP - 133
EP - 155
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 1
ER -