Unidad de Epidemiología Molecular (UEM), Instituto de Patología Experimental, Universidad Nacional de Salta-CONICET, Salta, Argentina.
Front Cell Infect Microbiol. 2021 May 31;11:663416. doi: 10.3389/fcimb.2021.663416. eCollection 2021.
, as other kinetoplastids, has a complex mechanism of editing of mitochondrial mRNAs that requires guide RNAs (gRNAs) coded in DNA minicircles in the kinetoplast. There are many variations on this mechanism among species. mRNA editing and gRNA repertoires are almost unknown in . Here, gRNAs were inferred based on deep-sequenced minicircle hypervariable regions (mHVRs) and editing cascades were rebuilt in strains belonging to the six main lineages. Inferred gRNAs were clustered according to their sequence similarity to constitute gRNA classes. Extreme diversity of gRNA classes was observed, which implied highly divergent gRNA repertoires among different lineages, even within some lineages. In addition, a variable gRNA class redundancy (i.e., different gRNA classes editing the same mRNA region) was detected among strains. Some strains had upon four times more gRNA classes than others. Such variations in redundancy affected gRNA classes of all mRNAs in a concerted way, i.e., there are correlated variations in the number of gRNAs classes editing each mRNA. Interestingly, cascades were incomplete for components of the respiratory complex I in several strains. Finally, gRNA classes of different strains may potentially edit mitochondrial mRNAs from other lineages in the same way as they edit their own mitochondrial mRNAs, which is a prerequisite for biparental inheritance of minicircle in hybrids. We propose that genetic exchange and biparental inheritance of minicircles combined with minicircle drift due to (partial) random segregation of minicircles during kDNA replication is a suitable hypothesis to explain the divergences among strains and the high levels of gRNA redundancy in some strains. In addition, our results support that the complex I may not be required in some stages in the life cycle as previously shown and that linkage (in the same minicircle) of gRNAs that edit different mRNAs may prevent gRNA class lost in such stage.
与其他动基体目生物一样,具有复杂的线粒体 mRNA 编辑机制,该机制需要 DNA 微环编码的指导 RNA(gRNA)。在不同物种中,这种机制存在许多变体。在 中,mRNA 编辑和 gRNA 库几乎未知。在这里,根据深度测序的微环高变区(mHVR)推断 gRNA,并在属于六个主要 谱系的菌株中重建编辑级联。推断的 gRNA 根据其序列相似性进行聚类,以构成 gRNA 类。观察到 gRNA 类的极端多样性,这表明不同谱系之间的 gRNA 库存在高度差异,甚至在某些谱系内也是如此。此外,在菌株之间检测到可变的 gRNA 类冗余(即,不同的 gRNA 类编辑同一 mRNA 区域)。一些菌株的 gRNA 类比其他菌株多四倍。这种冗余的变化以协同的方式影响所有 mRNA 的 gRNA 类,即编辑每个 mRNA 的 gRNA 类的数量存在相关变化。有趣的是,在几个菌株中,呼吸复合物 I 的成分的级联是不完整的。最后,不同菌株的 gRNA 类可能以与编辑自身线粒体 mRNA 相同的方式编辑来自同一谱系的线粒体 mRNA,这是杂种中线粒体微环双亲遗传的前提。我们提出,遗传交换和微环的双亲遗传以及由于 kDNA 复制过程中微环的(部分)随机分离导致的微环漂移是解释菌株间差异和某些菌株中 gRNA 冗余水平高的合适假设。此外,我们的结果支持复杂 I 在生命周期的某些阶段可能不需要,如先前所示,并且编辑不同 mRNA 的 gRNA 之间的连接(在同一微环中)可能防止此类阶段中 gRNA 类的丢失。