The half-life of the F1-ATPase β-subunit (F1-β) mRNA in ATPase-poor brown adipose tissue (BAT) (t?? = 9.5 h) was found to be 3–7-fold shorter than in liver (t?? = 27 h) and heart (t?? = 63 h) of mice. When translated in reticulocyte lysate, a 2–3-fold lower efficiency appeared with F1-β mRNA from BAT than from other tissues. The in vitro synthesized F1-β protein precursors of BAT, liver and heart origin were imported and processed by mouse liver mitochondria with equal efficiency. The results indicate that the pool or abundant F1-β mRNA in BAT is not fully translatable most likely due to its low metabolic stability.