Takahashi Y, Urushiyama S, Tani T, Ohshima Y
Department of Biology, Faculty of Science, Kyushu University, Fukuoka, Japan.
Mol Cell Biol. 1993 Sep;13(9):5613-9. doi: 10.1128/mcb.13.9.5613-5619.1993.
Splicing an mRNA precursor requires multiple factors involving five small nuclear RNA (snRNA) species called U1, U2, U4, U5, and U6. The presence of mRNA-type introns in the U6 snRNA genes of some yeasts led to the hypothesis that U6 snRNA may play a catalytic role in pre-mRNA splicing and that the U6 introns occurred through reverse splicing of an intron from an mRNA precursor into a catalytic site of U6 snRNA. We characterized the U2 snRNA gene of the yeast Rhodotorula hasegawae, which has four mRNA-type introns in the U6 snRNA gene, and found an mRNA-type intron of 60 bp. The intron of the U2 snRNA gene is present in the highly conserved region immediately downstream of the branch site recognition domain. Interestingly, we found that this region can form a novel base pairing with U6 snRNA. We discuss the possible implications of these findings for the mechanisms of intron acquisition and for the role of U2 snRNA in pre-mRNA splicing.
剪接mRNA前体需要多种因子,其中包括五种被称为U1、U2、U4、U5和U6的小核RNA(snRNA)。一些酵母的U6 snRNA基因中存在mRNA型内含子,这引发了一种假说,即U6 snRNA可能在mRNA前体剪接中起催化作用,并且U6内含子是通过将一个内含子从mRNA前体反向剪接到U6 snRNA的催化位点而产生的。我们对哈氏红酵母的U2 snRNA基因进行了表征,该基因在U6 snRNA基因中有四个mRNA型内含子,并发现了一个60 bp的mRNA型内含子。U2 snRNA基因的内含子位于分支位点识别域下游紧邻的高度保守区域。有趣的是,我们发现该区域可以与U6 snRNA形成一种新的碱基配对。我们讨论了这些发现对内含子获得机制以及U2 snRNA在mRNA前体剪接中作用的可能影响。