Limited DNase I Nicking As a Probe of Gene Conformation
Overview
Authors
Affiliations
We have extended the use of pancreatic DNase I as a probe of chromatin structure by exploring the accessibility of an active gene to the introduction of the first single-stranded nick. We show by a target analysis that the beta-globin gene is about 25-fold more sensitive to single-site nicking than is an average sequence in the chicken erythrocyte nucleus or the nontranscribed albumin gene. The sites of initial DNase I nicking are shown to cluster within the transcribed sequence of the beta-globin gene.
Vayda M, Freeling M Plant Mol Biol. 2013; 6(6):441-54.
PMID: 24307421 DOI: 10.1007/BF00027136.
Longacre S, Hibner U, Raibaud A, Eisen H, Baltz T, Giroud C Mol Cell Biol. 1983; 3(3):399-409.
PMID: 6843549 PMC: 368548. DOI: 10.1128/mcb.3.3.399-409.1983.
Analysis of chromatin of skeletal muscle of developing rats using micrococcal nuclease and DNase I.
Pandey R, Kanungo M Mol Biol Rep. 1984; 9(4):245-51.
PMID: 6708951 DOI: 10.1007/BF00775356.
Massol N, LEBEAU M, Baulieu E Biochem J. 1984; 217(1):309-16.
PMID: 6320802 PMC: 1153211. DOI: 10.1042/bj2170309.
Felber B, Weber R, Ryffel G Nucleic Acids Res. 1981; 9(11):2475-94.
PMID: 6269051 PMC: 326865. DOI: 10.1093/nar/9.11.2475.