Skip Navigation

This Article
Right arrow Print PDF (2315K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (7)
Right arrowRequest Permissions
Citing Articles
Right arrowScopus Links
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Wayne, R. L.
Right arrow Articles by Procunier, J. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wayne, R. L.
Right arrow Articles by Procunier, J. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1985, Vol. 13, No. 8 2869-2879
© 1985


Articles

Preferential DNase I sensitivity of insert-free ribosomal RNA repeats of Drosophila melanogaster

Richard L. Wayne, Z.Dave Sharp* and James D. Procunier

Biology Department, Rice University Houston, TX 77005, USA

Received November 7, 1984. Revised March 15, 1985. Accepted March 15, 1985.

The five predominant types of rDNA repeats in D. melanogaster were analyzed with respect to their DNase I sensitivity. Only the insert-free repeats showed a generalized DNase I sensitivity pattern whereas the major type I, both minor type I and type II repeats were not as extensively degraded by the nuclease. For XX and XY embryonic nuclei, where there is rapid cell division, the majority of the In repeats were DNase I sensitive. This indicated that these In repeats have the potential to be transcribed during this developmental stage. When compared to the In repeats, the chromatin configuration of the In+ repeats is indicative of a higher order of chromatin folding. The paucity of In+ primary gene transcripts observed in vivo could result from In+ repeats being packaged into a more condensed form of chromatin.


*Present address: Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USA


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
J. Ye and T. H. Eickbush
Chromatin Structure and Transcription of the R1- and R2-Inserted rRNA Genes of Drosophila melanogaster
Mol. Cell. Biol., December 1, 2006; 26(23): 8781 - 8790.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
D. G. Eickbush and T. H. Eickbush
Transcription of Endogenous and Exogenous R2 Elements in the rRNA Gene Locus of Drosophila melanogaster
Mol. Cell. Biol., June 1, 2003; 23(11): 3825 - 3836.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.