Schindewolf C A, Domdey H
Institut für Biochemie, Genzentrum, Ludwig-Maximilians-Universität München, Germany.
Nucleic Acids Res. 1995 Apr 11;23(7):1133-9. doi: 10.1093/nar/23.7.1133.
We have tested the fate of a circularized synthetic pre-mRNA transcript in a whole cell splicing extract of Saccharomyces cerevisiae. Our results demonstrate that this circular precursor RNA is able to induce spliceosome formation in vitro and that the products of the following splicing reaction are the lariat-shaped intron, and a mature circular mRNA. Thus, it would appear that free 5' and/or 3' ends are not obligatory for a splicing reaction to occur, although we find its efficiency to be strongly influenced by the presence or lack of free ends. To our knowledge, this is the first demonstration that a circular pre-mRNA molecule is recognized as a suitable substrate by an eukaryotic mRNA splicing apparatus.
我们已经在酿酒酵母的全细胞剪接提取物中测试了环化合成前体mRNA转录物的命运。我们的结果表明,这种环状前体RNA能够在体外诱导剪接体形成,并且后续剪接反应的产物是套索状内含子和成熟的环状mRNA。因此,虽然我们发现剪接反应的效率受到游离末端存在与否的强烈影响,但游离的5'和/或3'末端对于剪接反应的发生似乎并非必不可少。据我们所知,这是首次证明环状前体mRNA分子被真核mRNA剪接装置识别为合适的底物。