Carmona M C, Valmaseda A, Brun S, Viñas O, Mampel T, Iglesias R, Giralt M, Villarroya F
Departament de Bioquimica i Biologia Molecular, Universitat de Barcelona, Spain.
Biochem Biophys Res Commun. 1998 Feb 4;243(1):224-8. doi: 10.1006/bbrc.1998.8088.
The expression of the two novel uncoupling proteins genes, UCP2 and UCP3, is differentially regulated during prenatal maturation of brown adipose tissue in the mouse. UCP2 gene is expressed early in prenatal development, when neither UCP1 nor UCP3 gene expression yet occurs. UCP3 mRNA is absent at any stage of fetal life; it appears suddenly at birth and reaches adult levels in a few hours. UCP2 mRNA increased after birth but more slowly than UCP3 and UCP1 mRNA. Short-time exposure of adult mice to cold caused a rise in UCP2 or UCP1 mRNA levels but not in that of UCP3. The postnatal rise in UCP2 gene expression appears to be a response to the thermic stress associated with birth, similarly to UCP1, whereas different biological signals may be responsible for the surge in UCP3 gene expression at birth.
在小鼠棕色脂肪组织的产前成熟过程中,两种新型解偶联蛋白基因UCP2和UCP3的表达受到不同的调控。UCP2基因在产前发育早期表达,此时UCP1和UCP3基因均未表达。UCP3 mRNA在胎儿期的任何阶段都不存在;它在出生时突然出现,并在数小时内达到成年水平。出生后UCP2 mRNA增加,但比UCP3和UCP1 mRNA增加得慢。成年小鼠短期暴露于寒冷环境会导致UCP2或UCP1 mRNA水平升高,但不会导致UCP3 mRNA水平升高。与UCP1类似,出生后UCP2基因表达的增加似乎是对与出生相关的热应激的一种反应,而不同的生物信号可能是出生时UCP3基因表达激增的原因。