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• W2495129043 abstract "The steroid hormones, including those secreted by the adrenal cortex (corticosteroids), the male sex hormones (androgens), and the female sex hormones (oestrogens and progestins), modify the metabolism of many cellular components in their respective target cells. Corticosteroids alter energy metabolism in a number of tissues and mineralocorticoids control electrolyte balance. The sex hormones are responsible for development and maintenance of reproductive tissue and secondary sexual characteristics. Controlling these functions at the cellular level requires that the hormones alter the production and activities of different cellular macromolecules. Regulation of steroid levels in the serum, of steroid actions on target cells, and of the mutual interactions of one steroid on another at the cellular level create the necessary balance in the above-mentioned steroid functions. This chapter briefly reviews recent investigations of the function of certain non-histone chromosomal proteins and DNA in the binding of the chick oviduct progesterone receptor (P-R) to nuclear binding sites (or nuclear ‘acceptor’ sites). During the course of these studies, significant modulations in the capacity of various preparations of the receptor to bind to these nuclear acceptor sites were observed. These modulations in nuclear binding were found to correlate with changes in one of the two subunits (monomers) of the P-R. No other physicochemical parameter, for example affinity of the steroid for the receptor, changes in sedimentation patterns, etc., was identified which distinguished the receptor with nuclear binding capacity from the receptor with no such activity." @default.
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• W2495129043 date "1981-01-01" @default.
• W2495129043 modified "2023-09-23" @default.
• W2495129043 title "Novel regulations in steroid action: role of receptor subunits and chromosomal proteins in nuclear binding" @default.
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• W2495129043 doi "https://doi.org/10.1007/978-1-349-05555-5_13" @default.
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