Fededa Juan P, Petrillo Ezequiel, Gelfand Mikhail S, Neverov Alexei D, Kadener Sebastián, Nogués Guadalupe, Pelisch Federico, Baralle Francisco E, Muro Andrés F, Kornblihtt Alberto R
Laboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, IFIBYNE-CONICET, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Buenos Aires, Argentina.
Mol Cell. 2005 Aug 5;19(3):393-404. doi: 10.1016/j.molcel.2005.06.035.
Alternative splicing plays a key role in generating protein diversity. Transfections with minigenes revealed coordination between two distant, alternatively spliced exons in the same gene. Mutations that either inhibit or stimulate inclusion of the upstream alternative exon deeply affect inclusion of the downstream one. However, similar mutations at the downstream alternative exon have little effect on the upstream one. This polar effect is promoter specific and is enhanced by inhibition of transcriptional elongation. Consistently, cells from mutant mice with either constitutive or null inclusion of a fibronectin alternative exon revealed coordination with a second alternative splicing region, located far downstream. Using allele-specific RT-PCR, we demonstrate that this coordination occurs in cis and is also affected by transcriptional elongation rates. Bioinformatics supports the generality of these findings, indicating that 25% of human genes contain multiple alternative splicing regions and identifying several genes with nonrandom distribution of mRNA isoforms at two alternative regions.
可变剪接在产生蛋白质多样性方面起着关键作用。用小基因转染揭示了同一基因中两个遥远的可变剪接外显子之间的协同作用。抑制或刺激上游可变外显子包含的突变会深刻影响下游外显子的包含。然而,下游可变外显子的类似突变对上游外显子影响很小。这种极性效应是启动子特异性的,并且通过抑制转录延伸而增强。一致地,来自具有纤连蛋白可变外显子组成型或无效包含的突变小鼠的细胞显示与位于下游很远的第二个可变剪接区域存在协同作用。使用等位基因特异性逆转录聚合酶链反应,我们证明这种协同作用发生在顺式中,并且也受转录延伸率的影响。生物信息学支持这些发现的普遍性,表明25%的人类基因包含多个可变剪接区域,并鉴定出几个在两个可变区域具有非随机mRNA异构体分布的基因。