Thomas J D, Conrad R C, Blumenthal T
Department of Biology Indiana University, Bloomington 47405.
Cell. 1988 Aug 12;54(4):533-9. doi: 10.1016/0092-8674(88)90075-x.
mRNA splicing in C. elegans is unusual: most introns are very short (approximately 50 bases), and many mRNAs receive a leader by trans-splicing. The donor in trans-splicing is a 94 nucleotide molecule, termed the leader RNA, that contributes its 5' 22 nucleotides to a variety of mRNAs. We show here that C. elegans has the usual snRNAs, which presumably catalyze the splicing reactions. As expected, they are bound to the Sm antigen and have 2,2,7-methylguanosine caps. Remarkably, the trans-spliced leader RNA is also Sm-associated and has this special cap. Hence, a molecule discovered as a substate of splicing has properties of molecules heretofore known only to facilitate splicing of other RNAs. Mature mRNAs that have received the leader evidently lack 2,2,7-methylguanosine caps, suggesting that these caps are removed or altered during processing.
秀丽隐杆线虫中的mRNA剪接情况不同寻常:大多数内含子非常短(约50个碱基),并且许多mRNA通过反式剪接获得一个前导序列。反式剪接中的供体是一个94个核苷酸的分子,称为前导RNA,它将其5'端的22个核苷酸贡献给多种mRNA。我们在此表明,秀丽隐杆线虫拥有常见的小核RNA(snRNA),推测其催化剪接反应。正如预期的那样,它们与Sm抗原结合并且具有2,2,7 - 甲基鸟苷帽。值得注意的是,反式剪接的前导RNA也与Sm相关并且具有这种特殊的帽。因此,一个作为剪接底物被发现的分子具有迄今为止仅知其有助于其他RNA剪接的分子的特性。已经获得前导序列的成熟mRNA显然缺乏2,2,7 - 甲基鸟苷帽,这表明这些帽在加工过程中被去除或改变。