School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Cells. 2019 Jul 10;8(7):696. doi: 10.3390/cells8070696.
Here we show that the serine/arginine rich splicing factor 2 (SRSF2) promotes cryptic 3' splice-site (3'AG') usage during cassette exon exclusion in survival of motor neuron (SMN2) minigenes. Deletion of the 3'AG' (3'AG'1), its associated branch point (BP') and polypyrimidine tract (PPT') sequences directs SRSF2 to promote a second 3'AG' (3'AG'2) with less conserved associated region for intron splicing. Furthermore, deletion of both 3'AG'1 and 3'AG'2 and their associated sequences triggered usage of a third 3'AG'3 that has very weak associated sequences. Interestingly, when intron splicing was directed to the 3'AG' cryptic splice-sites, intron splicing from the canonical 3'AG splice-site was reduced along with a decrease in cassette exon inclusion. Moreover, multiple SRSF2 binding sites within the intron are responsible for 3'AG' activation. We conclude that SRSF2 facilitates exon exclusion by activating a cryptic 3'AG' and inhibiting downstream intron splicing.
在这里,我们表明丝氨酸/精氨酸丰富的剪接因子 2(SRSF2)在运动神经元存活(SMN2)基因小基因的外显子剪接排除过程中促进隐蔽的 3'剪接位点(3'AG')的使用。删除 3'AG'(3'AG'1)、其相关的分支点(BP')和多嘧啶序列(PPT')序列指导 SRSF2 促进第二个 3'AG'(3'AG'2),其相关的区域对于内含子剪接的保守性较低。此外,删除 3'AG'1 和 3'AG'2 及其相关序列会触发第三个 3'AG'3 的使用,该序列的相关序列非常弱。有趣的是,当内含子剪接被导向隐蔽的 3'AG 剪接位点时,与外显子剪接的减少同时,来自规范 3'AG 剪接位点的内含子剪接也减少了。此外,内含子内的多个 SRSF2 结合位点负责 3'AG 的激活。我们得出结论,SRSF2 通过激活隐蔽的 3'AG 并抑制下游内含子剪接来促进外显子排除。