Bolton M C, Dudhia J, Bayliss M T
Biochemistry Division, Kennedy Institute of Rheumatology, Hammersmith, London, U.K.
Biochem J. 1996 Oct 15;319 ( Pt 2)(Pt 2):489-98. doi: 10.1042/bj3190489.
A competitive reverse transcriptase-PCR (RT-PCR) assay has been developed for the quantification of particular mRNA species in human articular cartilage. Competitor RNA species were synthesized that differed from the amplified target sequence only by the central insertion of an EcoRI restriction site. By using known amounts of synthetic target and competitor RNA, it was shown that competitor RNA molecules designed in this way are reverse-transcribed and amplified with equal efficiency to the target of interest. Furthermore quantification could be performed during the plateau phase of the PCR, which was necessary when using ethidium bromide fluorescence as a detection system. The inhibition of aggrecan and link-protein mRNA expression by interleukin 1 or tumour necrosis factor in monolayers of human articular chondrocytes quantified by this competitive RT-PCR method compared favourably with Northern hybridization studies. The main advantage of this technique is that it can be used to quantify levels of mRNA with RNA extracted directly from 100 mg wet weight of human articular cartilage. Age-related changes in aggrecan and link-protein mRNA were therefore quantified in human articular cartilage directly after dissection from the joint. The concentration of link-protein mRNA was higher in immature cartilage than in mature cartilage when expressed relative to the amount of glyceraldehyde-3-phosphate dehydrogenase mRNA, but no age-related changes were observed in aggrecan mRNA expression. The ratio of aggrecan to link-protein mRNA was higher in mature cartilage than in immature tissue. These age-related differences in the molecular stoichiometry of aggrecan and link-protein mRNA might have implications with respect to the regulation of the formation and the stability of the proteoglycan aggregates in cartilage.
已开发出一种竞争性逆转录聚合酶链反应(RT-PCR)检测方法,用于定量人关节软骨中特定的mRNA种类。合成了竞争RNA种类,其与扩增的靶序列的差异仅在于在中央插入了一个EcoRI限制性位点。通过使用已知量的合成靶标和竞争RNA,结果表明以这种方式设计的竞争RNA分子能够以与感兴趣的靶标相同的效率进行逆转录和扩增。此外,定量可在PCR的平台期进行,这在使用溴化乙锭荧光作为检测系统时是必要的。用这种竞争性RT-PCR方法定量检测白细胞介素1或肿瘤坏死因子对人关节软骨细胞单层中聚集蛋白聚糖和连接蛋白mRNA表达的抑制作用,与Northern杂交研究相比具有优势。该技术的主要优点是可用于定量从100mg湿重的人关节软骨直接提取的RNA中的mRNA水平。因此,在从关节解剖后直接对人关节软骨中聚集蛋白聚糖和连接蛋白mRNA的年龄相关变化进行了定量。相对于甘油醛-3-磷酸脱氢酶mRNA的量,连接蛋白mRNA在未成熟软骨中的浓度高于成熟软骨,但未观察到聚集蛋白聚糖mRNA表达的年龄相关变化。成熟软骨中聚集蛋白聚糖与连接蛋白mRNA的比率高于未成熟组织。聚集蛋白聚糖和连接蛋白mRNA分子化学计量的这些年龄相关差异可能对软骨中蛋白聚糖聚集体的形成和稳定性的调节具有影响。