Mol Biol Evol. 2010 Sep;27(9):1979-82. doi: 10.1093/molbev/msq087. Epub 2010 Apr 1.
The 2.9-Mbp genome of the microsporidian Encephalitozoon cuniculi is severely reduced and compacted, possessing only 16 known tiny spliceosomal introns. Based on motif and expression data, intron profiles were constructed to screen the genome. Twenty additional introns were predicted and verified, doubling the previous estimate. We further predict that accurate 3' splice site (3'SS) selection is accomplished via a scanning mechanism with specificity achieved by maintaining a constrained variable length between the branch point motif and 3'SS. Only introns in ribosomal protein genes exhibit positional bias, and we hypothesize that splicing could be regulating expression of these genes. The large set of new introns in non-ribosomal protein genes suggests that current models of intron loss are unlikely sufficient to explain the distribution of introns. Together, these results extend our understanding of the role of intron loss in genome evolution and contribute to a novel model for splice site selection.
微孢子虫脑炎新内共生体的 2.9-Mbp 基因组严重缩小和紧凑,仅拥有 16 个已知的微小剪接体内含子。基于模体和表达数据,构建内含子谱来筛选基因组。预测和验证了另外 20 个内含子,使之前的估计翻了一番。我们进一步预测,准确的 3'剪接位点 (3'SS) 选择是通过一种具有特异性的扫描机制来完成的,这种特异性通过保持分支点模体和 3'SS 之间的约束可变长度来实现。只有核糖体蛋白基因中的内含子表现出位置偏向,我们假设剪接可能调节这些基因的表达。大量新的非核糖体蛋白基因中的内含子表明,目前的内含子缺失模型不太可能足以解释内含子的分布。总之,这些结果扩展了我们对内含子缺失在基因组进化中的作用的理解,并为剪接位点选择提供了一个新的模型。