Arts G J, Sloof P, Benne R
E.C. Slater Institute, University of Amsterdam, Academic Medical Centre, The Netherlands.
Mol Biochem Parasitol. 1995 Jul;73(1-2):211-22. doi: 10.1016/0166-6851(95)00119-l.
Chimeric g(uide) RNA:pre-mRNA molecules are potential intermediates of the RNA editing process in kinetoplastid mitochondria. We have studied the characteristics of chimeric molecules formed in mitochondrial extracts of the insect trypanosomatid Crithidia fasciculata which had been supplied with synthetic NADH dehydrogenase (ND) subunit-7 gRNA and pre-mRNA variants. The ability of a gRNA to participate in chimera formation in this system depends on the possibility of base pairing with the pre-mRNA via the anchor sequence, but not on the presence of a U-tail or a full-length informational part. Chimeras formed with a specific gRNA:pre-mRNA pair displayed a large variation in length, due to variably sized 3' end truncations of the gRNA moieties and variation in the sites in the pre-mRNA to which the gRNAs were attached. Surprisingly, the presence of a U-tail in the gRNA for a large part determined the specificity of the linkage. In 60% of the cases gRNAs possessing a U-tail of at least one residue were attached to an editing site, whereas 75% of the gRNAs without Us were attached to non-editing sites. Furthermore, the chimera forming activity was greatly stimulated by the addition of ATP but not by AMP-CPP, an ATP-analogue with a non-hydrolyzable alpha-beta phosphate bond. This suggests the involvement in the chimera formation of an RNA ligase.
嵌合g(uide)RNA:前体mRNA分子是动基体线粒体中RNA编辑过程的潜在中间体。我们研究了在已提供合成烟酰胺腺嘌呤二核苷酸脱氢酶(ND)亚基7 gRNA和前体mRNA变体的昆虫锥虫克氏锥虫线粒体提取物中形成的嵌合分子的特性。在该系统中,gRNA参与嵌合体形成的能力取决于通过锚定序列与前体mRNA碱基配对的可能性,而不取决于U尾或全长信息部分的存在。由特定gRNA:前体mRNA对形成的嵌合体在长度上表现出很大差异,这是由于gRNA部分3'端截短大小可变以及gRNA连接到前体mRNA的位点不同所致。令人惊讶的是,gRNA中U尾的存在在很大程度上决定了连接的特异性。在60%的情况下,具有至少一个残基U尾的gRNA连接到编辑位点,而75%没有U的gRNA连接到非编辑位点。此外,添加ATP可极大地刺激嵌合体形成活性,但添加AMP-CPP(一种具有不可水解α-β磷酸键的ATP类似物)则不会。这表明RNA连接酶参与了嵌合体的形成。