Ouellett A J, Malt R A
Biochemistry. 1976 Jul 27;15(15):3358-61. doi: 10.1021/bi00660a029.
The stability of polyadenylated messenger ribonucleic acid(mRNA) from cytoplasmic structures sedimenting faster than 40S was analyzed in normal mouse kidney. Incorporation of radioactivity into poly(A)-containing and poly(A)-lacking cytoplasmic RNAs separated by oligo(dT)-cellulose chromatography was determined after sedimentation of RNA IN SODIUM DODECYL SULFATE CONTAINING SUCROSE DENSITY GRADIENTS. Radioactivity accumulated in poly(A)-containing RNA during the first 6 h and then decayed exponentially. Beginning 8-12h after administering label, two components were evident in the decay curve of poly(A)-containing RNA; the short-lived component (approximately 57% of newly synthesized molecules) had an apparent half-life of 6h, and the second class (approximately 43% of new mRNA) was more stable, decaying with a 24-h half-life. These studies provide the basis for examining the regulation of mRNA stability during compensatory renal hypertrophy.
在正常小鼠肾脏中分析了来自沉降速度快于40S的细胞质结构的聚腺苷酸化信使核糖核酸(mRNA)的稳定性。在含十二烷基硫酸钠的蔗糖密度梯度中对RNA进行沉降后,测定通过寡聚(dT)-纤维素色谱法分离的含聚(A)和不含聚(A)的细胞质RNA中放射性的掺入情况。放射性在最初6小时内积累在含聚(A)的RNA中,然后呈指数衰减。在给予标记物8 - 12小时后,含聚(A)的RNA的衰变曲线中出现两个组分;短寿命组分(约占新合成分子的57%)的表观半衰期为6小时,第二类(约占新mRNA的43%)更稳定,以24小时的半衰期衰变。这些研究为研究代偿性肾肥大过程中mRNA稳定性的调节提供了基础。