Veistinen Elli, Liippo Jussi, Lassila Olli
Department of Medical Microbiology, Turku Graduate School of Biomedical Sciences, University of Turku, Kiinamyllynkatu 13, Finland.
J Immunol Methods. 2002 Dec 20;271(1-2):113-23. doi: 10.1016/s0022-1759(02)00370-8.
Aiolos is a transcriptional regulator of B cell development and belongs to the Ikaros family of chromatin remodelling transcription factors. All the members of Ikaros family produce multiple isoforms via alternative mRNA splicing. Altered expression of Ikaros isoforms has been found in patients with acute lymphoblastic leukemia but it is not studied whether the altered expression of Aiolos isoforms also has a role in the development of leukemias or lymphomas. We developed a quantitative real-time PCR application to detect the relative expression of Aiolos splice variants. The method is based on fluorescence resonance energy transfer (FRET)-labelled isoform specific hybridisation probes used with the LightCycler instrument. The isoform specificity is obtained by targeting the probes at the edges of chosen exons. The probes are here shown to represent a rapid, high throughput, specific and reproducible quantification method. We designed and optimised the analysis for a dominant negative Aiolos isoform, but the described method is applicable to any isoform-forming gene. This study shows that the real-time PCR with exon edge spanning probe pairs can be applied generally to reveal the importance of alternative splicing and the role of isoforms in normal development and diseases.
Aiolos是B细胞发育的转录调节因子,属于染色质重塑转录因子的Ikaros家族。Ikaros家族的所有成员都通过可变mRNA剪接产生多种异构体。在急性淋巴细胞白血病患者中发现了Ikaros异构体的表达改变,但尚未研究Aiolos异构体的表达改变是否也在白血病或淋巴瘤的发生中起作用。我们开发了一种定量实时PCR应用来检测Aiolos剪接变体的相对表达。该方法基于与LightCycler仪器一起使用的荧光共振能量转移(FRET)标记的异构体特异性杂交探针。通过将探针靶向选定外显子的边缘来获得异构体特异性。此处显示这些探针代表了一种快速、高通量、特异性和可重复的定量方法。我们设计并优化了针对显性负性Aiolos异构体的分析,但所描述的方法适用于任何形成异构体的基因。这项研究表明,使用跨越外显子边缘的探针进行实时PCR通常可用于揭示可变剪接的重要性以及异构体在正常发育和疾病中的作用。