Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
1983-10-28
pubmed:abstractText
Electron microscopy shows that complexes of the single-strand DNA binding protein (SSB) of Escherichia coli and phage fd DNA appear as beaded fiber loops containing an average of 38 beads, 1 per 170 bases of DNA. Extensive digestion of native unfixed SSB-fd DNA complexes with micrococcal nuclease reveals a protected DNA fragment of 145 bases, while shorter digestion periods result in a sequence of fragments in multiples of 160 +/- 25 bases. Digestion of these complexes with DNase I produces a repeating pattern of bands, multiples of approximately 15 bases with strong bands at 60, 105, 118, 130, 145, 150, and 210 bases. Isopycnic banding in CsCl solution yields densities of 1.272 and 1.700 g/ml, respectively, for SSB alone and for fd DNA and, after fixation, of 1.388 g/ml for fd DNA-SSB beaded fibers and 1.373 g/ml for the individual protein-DNA beads. Based on these data and the molecular weights of SSB and fd DNA, we suggest that the nucleoprotein chain consists of eight molecules of SSB bound to 145 bases of DNA, with these units linked by roughly 30 bases of protein-free DNA. The excellent concord between results obtained by enzyme digestion of unfixed native samples and, after fixation, by electron microscopy and density banding supports the conclusion that SSB organizes single-stranded DNA in a manner similar to the organization of duplex DNA by histones.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-1090613, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-1092689, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-1103088, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-1103970, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-138139, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-168578, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-17754289, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-197496, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-221903, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-227832, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-269383, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-289456, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-340916, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-341152, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-4370363, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-441739, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-4422492, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-4566449, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-4610569, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6035921, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6160477, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6212122, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6244299, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6244589, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6278471, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-6449689, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-7028102, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-7046950, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-78683, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-790996, http://linkedlifedata.com/resource/pubmed/commentcorrection/6764531-792455
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:volume
79
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5803-7
pubmed:dateRevised
2010-9-13
pubmed:meshHeading
pubmed:year
1982
pubmed:articleTitle
Escherichia coli single-strand binding protein organizes single-stranded DNA in nucleosome-like units.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.