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Antigenically active nonhistone chromatin proteins in cancer cells

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dc.contributor.author Busch, Harris
dc.contributor.author Yeoman, Lynn C
dc.contributor.author Busch, Rose K
dc.contributor.author Jordan, John J
dc.contributor.author Rao, M R S
dc.contributor.author Taylor, Charles W
dc.contributor.author Wu, Benjamin C
dc.date.accessioned 2011-05-20T06:29:06Z
dc.date.available 2011-05-20T06:29:06Z
dc.date.issued 1976-09
dc.identifier 0008-5472 en_US
dc.identifier.citation Cancer Research 36, 3399-3408 (1976) en_US
dc.identifier.uri https://libjncir.jncasr.ac.in/xmlui/10572/117
dc.description Restricted access en_US
dc.description.abstract Two-dimensional polyacrylamide gel electrophoresis shows that in nuclei of Novikoff hepatoma ascites cells there are approximately 75 proteins in the chromatin fraction soluble in 3 m NaCl:7 m urea. Dialysis of this fraction to an ionic strength of 0.15 produces a soluble fraction and a precipitate. The proteins in the soluble fraction have been reported to be active in gene control. Antibodies to the soluble fraction distribute diffusely throughout the nucleus, and antibodies to the precipitate localized primarily in the nucleolus and the nuclear ribonucleoprotein network. The nucleolar proteins differ from the extranucleolar proteins in antigenicity and labeling patterns. The development of methods for isolation, purification, and identification of nuclear proteins provided the opportunity for analysis of chromatin antigens in tumor cells. Utilizing two-dimensional preparative polyacrylamide gel techniques as well as conventional procedures, several nuclear proteins have been isolated in electrophoretically homogeneous states including protein A-24, a histone-like nonhistone protein; C-14, a protein that stimulates nucleolar RNA polymerase; and a chromatin antigen soluble in 3 m NaCl:7 m urea that remains soluble after dialysis to 0.15 m NaCl to precipitate the histones and the DNA. This antigen has been found in the chromatin of both the Novikoff hepatoma and the Walker 256 carcinosarcoma but not in the chromatin of either normal or regenerating liver. It is a nonhistone nuclear protein as indicated by its amino acid analysis in which the ratio of the number of acidic to basic amino acids is approximately 1.4. Further studies are in progress on the function and structure of this chromatin protein. As an approach to analysis of relative rates of synthesis of this antigen and other proteins, the products of translation of messenger RNA of Novikoff hepatoma and normal liver are being analyzed by autoradiography of two-dimensional electrophoretic gels. en_US
dc.description.uri http://dx.doi.org/cancerres.aacrjournals.org/content/36/9_Part_2/3399 en_US
dc.language.iso en en_US
dc.publisher American Association for Cancer Research en_US
dc.rights © 1976 American Association for Cancer Research en_US
dc.subject Antigenically Active Nonhistone Chromatin Proteins en_US
dc.subject Cancer Cells en_US
dc.subject Cancer en_US
dc.subject Chromatin en_US
dc.subject Proteins en_US
dc.title Antigenically active nonhistone chromatin proteins in cancer cells en_US
dc.type Article en_US


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