The cellular process by which testosterone, after binding to its specific intracellular androgen receptor (AR), influences the expression of target genes within the cell nucleus. This transcription is the fundamental molecular mechanism driving the hormone’s anabolic effects, including muscle protein synthesis, bone density maintenance, and red blood cell production. The efficacy of testosterone signaling is dependent not only on circulating hormone levels but also on the functional integrity of the AR and the efficiency of this transcription.
Origin
This concept integrates molecular biology with endocrinology, detailing the specific non-genomic and genomic actions of steroid hormones. The understanding of testosterone’s direct influence on DNA transcription was a major breakthrough in explaining its profound physiological effects on target tissues. This mechanism is central to the clinical use of androgens in hormonal health.
Mechanism
Once testosterone enters a target cell, it either binds directly to the AR or is converted to the more potent dihydrotestosterone (DHT) before binding. The activated hormone-receptor complex then translocates to the nucleus, where it binds to specific DNA sequences called hormone response elements (HREs). This binding acts as a transcription factor, recruiting co-activator proteins to initiate or suppress the transcription of specific messenger RNA (mRNA) molecules, ultimately altering the cell’s protein synthesis profile.
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