Lei Haixin, Vorechovsky Igor
University of Southampton School of Medicine, Division of Human Genetics, Duthie Building, UK.
Mol Cell Biol. 2005 Aug;25(16):6912-20. doi: 10.1128/MCB.25.16.6912-6920.2005.
Auxiliary splicing signals in introns play an important role in splice site selection, but these elements are poorly understood. We show that a subset of serine/arginine (SR)-rich proteins activate a cryptic 3' splice site in a sense Alu repeat located in intron 4 of the human LST1 gene. Utilization of this cryptic splice site is controlled by juxtaposed Alu-derived splicing silencers and enhancers between closely linked short tandem repeats TNFd and TNFe. Systematic mutagenesis of these elements showed that AG dinucleotides that were not preceded by purine residues were critical for repressing exon inclusion of a chimeric splicing reporter. Since the splice acceptor-like sequences are present in excess in exonic splicing silencers, these signals may contribute to inhibition of a large number of pseudosites in primate genomes.
内含子中的辅助剪接信号在剪接位点选择中起重要作用,但对这些元件的了解甚少。我们发现,富含丝氨酸/精氨酸(SR)的蛋白质子集激活了人类LST1基因第4内含子中一个有义Alu重复序列内的一个隐蔽3'剪接位点。该隐蔽剪接位点的利用受紧密连锁的短串联重复序列TNFd和TNFe之间并列的Alu衍生剪接沉默子和增强子控制。对这些元件的系统诱变表明,嘌呤残基之前不存在的AG二核苷酸对于抑制嵌合剪接报告基因的外显子包含至关重要。由于剪接受体样序列在外显子剪接沉默子中大量存在,这些信号可能有助于抑制灵长类基因组中的大量假位点。