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The response of rat thymus nuclei to thyroid hormones

The effect of triiodothyronine (L-T₃) on the protein, RNA and DNA fractions of the thymus nuclei of growth-arrested sulfaguanidine-fed rats has been studied.

A single dose of 15 µg of L-T₃ stimulated the incorporation of ¹⁴C-labelled amino acids into total nuclear protein, whole histone and histone fractions. The incorporation of the labelled amino acid into nuclear protein was increased 40 percent over the control 4 hours after the administration of L-T₃. The incorporation of alanine-1-¹⁴C into the total histone fraction reached a maximum 4 hours after the administration of L-T₃ and then decreased 8 and 16 hours after the administration of L-T₃. The incorporation of alanine-1-¹⁴C into histone fraction f₁ reached a maximum at 4 hours after the administration of L-T₃ while the incorporation into fractions f<sub>2a</sub>, f<sub>2b</sub> and f₃ did not reach a maximum until 8 hours after the administration of L-T₃.

Time course studies showed that the protein and RNA moieties of thymus chromatin of rats injected with a single dose of L-T₃ was increased to a maximum at 4 hours. The T<sub>m</sub> of chromatin was increased 2° by L-T₃ administration as early as 2 hours. However, the T<sub>m</sub> of DNA was not affected.

Four hours after the administration of L-T₃ the template efficiency increased 171 percent. The template efficiency of DNA was not affected by L-T₃.

These results demonstrate that thyroid hormones modify the chromatin in such a way that the template efficiency is increased. An hypothesis for the mechanism of thyroid hormone action was presented. / Ph. D.

Identiferoai:union.ndltd.org:VTETD/oai:vtechworks.lib.vt.edu:10919/37198
Date13 January 2010
CreatorsRuark, Edwin Warren
ContributorsBiochemistry and Nutrition
PublisherVirginia Tech
Source SetsVirginia Tech Theses and Dissertation
LanguageEnglish
Detected LanguageEnglish
TypeDissertation, Text
Format89 leaves, BTD, application/pdf, application/pdf
RightsIn Copyright, http://rightsstatements.org/vocab/InC/1.0/
RelationOCLC# 22366655, LD5655.V856_1970.R8.pdf

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