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Studies on nonhistone chromosomal proteins

Date Issued
August 1, 1980
Author(s)
Savin, Thomas J.
Advisor(s)
W. K. Yang
Additional Advisor(s)
R. W. Tennant
M. P. Stulberg
Permanent URI
https://trace.tennessee.edu/handle/20.500.14382/37398
Abstract
In the first part of this study, nonhistone chromosomal proteins were examined for possible age-associated alteration in Fisher 344 rats. Various nonhistone chromosomal protein fractions were isolated from brain and liver tissues of 4- and 29-month-old rats and analyzed either by two-dimensional gel electrophoresis or by sodium dodecyl sulfatepolyacrylimide gel electrophoresis. I detected no age-related differences in the nonhistone protein complement. However, tissue-specific differences (between the liver and the brain) and sex-specific differences (between male and female rat brains) in nonhistone proteins were revealed. The 5 M urea soluble nonhistone protein fraction isolated from male rat brain contains 12 detectable proteins that are not present in the similar fraction from the female.

In the second part of this study, possible alteration of nonhistone chromosomal proteins during infection of NIH 3T3 cells with murine leukemia virus (MuLV) was investigated. Sucrose gradient analyses of viral DNAs reveal that MuLV DNA is in the form of a nucleoprotein complex, which was distinctly different from the minichromosome form found with the SV40 viral DNA. It was also found that circular forms of MuLV DNAs could be extracted from host chromatin with O.35 M NaCl. This is the same salt concentration that removes a large portion of nonhistone proteins from chromatin. This suggests the possibility of interaction between viral DNA and loosely bound nonhistone proteins. Also, various cellular protein fractions, including the nonhistone protein fractions, were isolated from NIH 3T3 cells which were uninfected, acutely infected, and chronically infected with MuLV. These proteins, which were 3[H] leucine labeled, were subjected to various electrophoretic analyses. Numerous differences in the protein complement isolated from the three groups of NIH 3T3 cells were observed. The major differences were present between the chronically infected cell group and the other two groups of cells.

Degree
Master of Science
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Thesis80S2292.pdf

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