Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.
BMC Evol Biol. 2011 Dec 19;11:364. doi: 10.1186/1471-2148-11-364.
It is widely accepted that orthologous genes have lost or gained introns throughout evolution. However, the specific mechanisms that generate these changes have proved elusive. Introns are known to affect nearly every level of gene expression. Therefore, understanding their mechanism of evolution after their initial fixation in eukaryotes is pertinent to understanding the means by which organisms develop greater regulation and complexity.
To investigate possible mechanisms of intron gain and loss, we identified 189 intron gain and 297 intron loss events among 11 Drosophila species. We then investigated these events for signatures of previously proposed mechanisms of intron gain and loss. This work constitutes the first comprehensive study into the specific mechanisms that may generate intron gains and losses in Drosophila. We report evidence of intron gain via transposon insertion; the first intron loss that may have occurred via non-homologous end joining; intron gains via the repair of a double strand break; evidence of intron sliding; and evidence that internal or 5' introns may not frequently be deleted via the self-priming of reverse transcription during mRNA-mediated intron loss. Our data also suggest that the transcription process may promote or result in intron gain.
Our findings support the occurrence of intron gain via transposon insertion, repair of double strand breaks, as well as intron loss via non-homologous end joining. Furthermore, our data suggest that intron gain may be enabled by or due to transcription, and we shed further light on the exact mechanism of mRNA-mediated intron loss.
人们普遍认为,在进化过程中,同源基因已经失去或获得了内含子。然而,产生这些变化的具体机制一直难以捉摸。内含子已知会影响基因表达的几乎每一个层面。因此,了解它们在真核生物中最初固定后进化的机制,对于理解生物如何发展出更大的调控和复杂性是至关重要的。
为了研究内含子获得和丢失的可能机制,我们在 11 种果蝇物种中鉴定出了 189 个内含子获得事件和 297 个内含子丢失事件。然后,我们研究了这些事件是否存在先前提出的内含子获得和丢失机制的特征。这项工作构成了首次对可能导致果蝇中内含子获得和丢失的具体机制的全面研究。我们报告了通过转座子插入导致内含子获得的证据;第一个可能通过非同源末端连接发生的内含子丢失;通过双链断裂修复导致的内含子获得;内含子滑动的证据;以及内部或 5'内含子可能不会经常通过 mRNA 介导的内含子丢失过程中逆转录的自我引发而被删除的证据。我们的数据还表明,转录过程可能促进或导致内含子获得。
我们的发现支持通过转座子插入、双链断裂修复以及非同源末端连接导致内含子丢失的发生。此外,我们的数据表明,内含子获得可能是由转录引发或促成的,我们进一步阐明了 mRNA 介导的内含子丢失的确切机制。