Akerman Martin, Mandel-Gutfreund Yael
Department of Biology, Technion-Institute of Technology, Haifa 32000, Israel.
Nucleic Acids Res. 2006 Jan 3;34(1):23-31. doi: 10.1093/nar/gkj408. Print 2006.
Alternative splicing (AS) constitutes a major mechanism creating protein diversity in humans. Previous bioinformatics studies based on expressed sequence tag and mRNA data have identified many AS events that are conserved between humans and mice. Of these events, approximately 25% are related to alternative choices of 3' and 5' splice sites. Surprisingly, half of all these events involve 3' splice sites that are exactly 3 nt apart. These tandem 3' splice sites result from the presence of the NAGNAG motif at the acceptor splice site, recently reported to be widely spread in the human genome. Although the NAGNAG motif is common in human genes, only a small subset of sites with this motif is confirmed to be involved in AS. We examined the NAGNAG motifs and observed specific features such as high sequence conservation of the motif, high conservation of approximately 30 bp at the intronic regions flanking the 3' splice site and overabundance of cis-regulatory elements, which are characteristic of alternatively spliced tandem acceptor sites and can distinguish them from the constitutive sites in which the proximal NAG splice site is selected. Our findings imply that AS at tandem splice sites and constitutive splicing of the distal NAG are highly regulated.
可变剪接(AS)是在人类中产生蛋白质多样性的一种主要机制。以往基于表达序列标签和mRNA数据的生物信息学研究已经鉴定出许多在人类和小鼠之间保守的AS事件。在这些事件中,约25%与3'和5'剪接位点的可变选择有关。令人惊讶的是,所有这些事件中有一半涉及相隔恰好3个核苷酸的3'剪接位点。这些串联的3'剪接位点是由于受体剪接位点处存在NAGNAG基序导致的,最近报道该基序在人类基因组中广泛分布。尽管NAGNAG基序在人类基因中很常见,但只有一小部分具有该基序的位点被证实参与了可变剪接。我们研究了NAGNAG基序,并观察到了一些特定特征,如该基序的高序列保守性、3'剪接位点侧翼内含子区域约30bp的高度保守性以及顺式调控元件的过量存在,这些都是可变剪接串联受体位点的特征,并且可以将它们与选择近端NAG剪接位点的组成型位点区分开来。我们的研究结果表明,串联剪接位点处的可变剪接和远端NAG的组成型剪接受到高度调控。