A Packing Mechanism for Nucleosome Organization Reconstituted Across a Eukaryotic Genome

Near the 5′ end of most eukaryotic genes, nucleosomes form highly regular arrays that begin at canonical distances from the transcriptional start site. Determinants of this and other aspects of genomic nucleosome organization have been ascribed to statistical positioning, intrinsically DNA-encoded p...

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Published inScience (American Association for the Advancement of Science) Vol. 332; no. 6032; pp. 977 - 980
Main Authors Zhang, Zhenhai, Wippo, Christian J., Wal, Megha, Ward, Elissa, Korber, Philipp, Pugh, B. Franklin
Format Journal Article
LanguageEnglish
Published Washington, DC American Association for the Advancement of Science 20.05.2011
The American Association for the Advancement of Science
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Summary:Near the 5′ end of most eukaryotic genes, nucleosomes form highly regular arrays that begin at canonical distances from the transcriptional start site. Determinants of this and other aspects of genomic nucleosome organization have been ascribed to statistical positioning, intrinsically DNA-encoded positioning, or some aspect of transcription initiation. Here, we provide evidence for a different explanation. Biochemical reconstitution of proper nucleosome positioning, spacing, and occupancy levels was achieved across the 5′ ends of most yeast genes by adenosine triphosphate—dependent trans-acting factors. These transcription-independent activities override DNA-intrinsic positioning and maintain uniform spacing at the 5′ ends of genes even at low nucleosome densities. Thus, an active, nonstatistical nucleosome packing mechanism creates chromatin organizing centers at the 5′ ends of genes where important regulatory elements reside.
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These authors contributed equally to this work.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.1200508