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Switched alternative splicing of oncogene CoAA during embryonal carcinoma stem cell differentiation

机译:癌基因干细胞分化过程中癌基因CoAA的交替剪接

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Alternative splicing produces functionally distinct proteins participating in cellular processes including differentiation and development. CoAA is a coactivator that regulates transcription-coupled splicing and its own pre-mRNA transcript is alternatively spliced. We show here that the CoAA gene is embryonically expressed and alternatively spliced in multiple tissues to three splice variants, CoAA, CoAM and CoAR. During retinoic-acid-induced P19 stem cell differentiation, the expression of CoAA undergoes a rapid switch to its dominant negative splice variant CoAM in the cavity of the embryoid body. CoAM functionally inhibits CoAA, and their switched expression up-regulates differentiation marker Sox6. Using a CoAA minigene cassette, we find that the switched alternative splicing of CoAA and CoAM is regulated by the cis-regulating sequence upstream of the CoAA basal promoter. Consistent to this, we show that p54(nrb) and PSF induce CoAM splice variant through the cis-regulating sequence. We have previously shown that the CoAA gene is amplified in human cancers with a recurrent loss of this cis-regulating sequence. These results together suggest that the upstream regulatory sequence contributes to alternative splicing of the CoAA gene during stem cell differentiation, and its selective loss in human cancers potentially deregulates CoAA alternative splicing and alters stem cell differentiation.
机译:选择性剪接产生参与细胞过程包括分化和发育的功能上不同的蛋白质。 CoAA是调节转录偶联剪接的辅助激活剂,其自身的前mRNA转录本也可以剪接。我们在此处显示CoAA基因在胚胎中表达,并在多个组织中选择性剪接成三个剪接变体,即CoAA,CoAM和CoAR。在视黄酸诱导的P19干细胞分化过程中,CoAA的表达在胚状体腔中迅速转变为其显性负剪接变体CoAM。 CoAM在功能上抑制了CoAA,并且它们的转换表达上调了分化标记Sox6。使用CoAA的小基因盒,我们发现CoAA和CoAM的切换的选择性剪接是由CoAA基础启动子上游的顺式调控序列调控的。与此一致,我们表明p54(nrb)和PSF通过顺式调控序列诱导CoAM剪接变体。先前我们已经表明,CoAA基因在人类癌症中被扩增,并反复失去该顺式调节序列。这些结果共同表明,上游调节序列在干细胞分化过程中有助于CoAA基因的选择性剪接,在人类癌症中的选择性丧失可能会破坏CoAA选择性剪接并改变干细胞的分化。

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