Shimada Makoto K, Sasaki-Haraguchi Noriko, Mayeda Akila
Division of Gene Expression Mechanism, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.
Matsunami Research Park (Sosai-kouseikai), 10 Izumi-cho, Kasamatsu-cho, Hashima-gun, Gifu 501-6061, Japan.
Int J Mol Sci. 2015 May 7;16(5):10376-88. doi: 10.3390/ijms160510376.
According to the length distribution of human introns, there is a large population of short introns with a threshold of 65 nucleotides (nt) and a peak at 85 nt. Using human genome and transcriptome databases, we investigated the introns shorter than 66 nt, termed ultra-short introns, the identities of which are scarcely known. Here, we provide for the first time a list of bona fide human ultra-short introns, which have never been characterized elsewhere. By conducting BLAST searches of the databases, we screened 22 introns (37-65 nt) with conserved lengths and sequences among closely related species. We then provide experimental and bioinformatic evidence for the splicing of 15 introns, of which 12 introns were remarkably G-rich and 9 introns contained completely inefficient splice sites and/or branch sites. These unorthodox characteristics of ultra-short introns suggest that there are unknown splicing mechanisms that differ from the well-established mechanism.
根据人类内含子的长度分布,存在大量短内含子,其阈值为65个核苷酸(nt),峰值在85 nt处。利用人类基因组和转录组数据库,我们研究了长度小于66 nt的内含子,即超短内含子,其特性鲜为人知。在此,我们首次提供了一份真正的人类超短内含子列表,这些内含子在其他地方从未被表征过。通过对数据库进行BLAST搜索,我们筛选出了22个在近缘物种中具有保守长度和序列的内含子(37 - 65 nt)。然后,我们为15个内含子的剪接提供了实验和生物信息学证据,其中12个内含子富含G,9个内含子含有完全无效的剪接位点和/或分支位点。超短内含子的这些非传统特征表明,存在与成熟机制不同的未知剪接机制。