Alternative splicing in exon 9 of glucocorticoid receptor pre-mRNA is regulated by SRp40

XB Yan, CH Tang, Y Huang, H Fang, ZQ Yu… - Molecular biology …, 2010 - Springer
XB Yan, CH Tang, Y Huang, H Fang, ZQ Yu, LM Wu, RY Liu
Molecular biology reports, 2010Springer
Increasing evidence indicates that alternative splicing of human glucocorticoid receptor (GR)
transcripts is implicated in the development of glucocorticoid resistance but the underlying
mechanism was not well known. Serine/arginine-rich (SR) proteins and heterogeneous
nuclear ribonucleoprotein (hnRNP) A1 play an important role in the spliceosome assembly.
In this study, we analyzed the effects of different SR proteins and hnRNP A1 on the
alternative splicing of GR pre-mRNA in HeLa and 293T cells using a minigene transfection …
Abstract
Increasing evidence indicates that alternative splicing of human glucocorticoid receptor (GR) transcripts is implicated in the development of glucocorticoid resistance but the underlying mechanism was not well known. Serine/arginine-rich (SR) proteins and heterogeneous nuclear ribonucleoprotein (hnRNP) A1 play an important role in the spliceosome assembly. In this study, we analyzed the effects of different SR proteins and hnRNP A1 on the alternative splicing of GR pre-mRNA in HeLa and 293T cells using a minigene transfection assay. Our results revealed that only SRp40 could induce a GRα to GRβ shift of pre-mRNA splicing in exon 9 in HeLa cells and this effect induced by SRp40 was further confirmed by small interfering RNA study. However, in 293T cells, SRp40 could not induce this shift. These results indicated that SRp40 may influence the alternative splicing of GR pre-mRNA to regulate the ratio of GRα to GRβ, and this effect is cell-dependent.
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