Duan Ye, Segev Tomer, Veksler-Lublinsky Isana, Ambros Victor, Srivastava Mansi
bioRxiv. 2024 Dec 2:2024.12.01.626237. doi: 10.1101/2024.12.01.626237.
The acoel worm has recently emerged as a model organism for studying whole-body regeneration and embryonic development. Previous studies suggest that post-transcriptional mechanisms likely play important roles in whole-body regeneration. Here, we establish a resource for studying microRNA-mediated gene regulation, a major aspect of post-transcriptional control in animals. Using small RNA-sequencing samples spanning key developmental stages, we annotated microRNAs. Our analysis uncovered a total of 1,050 microRNA loci, including 479 high-confidence loci based on structural and read abundance criteria. Comparison of microRNA seed sequences with those in other bilaterian species revealed that encodes the majority of known conserved bilaterian microRNA families and that several microRNA families previously reported only in protostomes or deuterostomes likely have ancient bilaterian origins. We profiled the expression dynamics of the miRNAs across embryonic and post-embryonic development. We observed that the and microRNAs are unconventionally enriched at early embryonic stages. To generate hypotheses for miRNA function, we annotated the 3' UTRs of protein-coding genes and performed miRNA target site predictions. Focusing on genes that are known to function in the wound response, posterior patterning, and neural differentiation in , we found that these processes may be under substantial miRNA regulation. Notably, we found that miRNAs in MIR-7 and MIR-9 families which have target sites in the posterior genes , , and are indeed expressed in the anterior of the animal, consistent with a repressive effect on their corresponding target genes. Our annotation offers candidate miRNAs for further functional investigation, providing a resource for future studies of post-transcriptional control during development and regeneration.
无肠蠕虫最近已成为研究全身再生和胚胎发育的模式生物。先前的研究表明,转录后机制可能在全身再生中发挥重要作用。在这里,我们建立了一个用于研究微小RNA介导的基因调控的资源库,这是动物转录后控制的一个主要方面。利用跨越关键发育阶段的小RNA测序样本,我们注释了微小RNA。我们的分析共发现了1050个微小RNA基因座,其中479个是基于结构和读数丰度标准的高可信度基因座。将微小RNA种子序列与其他两侧对称动物物种的序列进行比较后发现,该生物编码了大多数已知的保守两侧对称动物微小RNA家族,并且几个先前仅在原口动物或后口动物中报道过的微小RNA家族可能起源于古老的两侧对称动物。我们分析了这些微小RNA在胚胎发育和胚后发育过程中的表达动态。我们观察到,某些微小RNA在胚胎早期阶段异常富集。为了生成关于微小RNA功能的假设,我们注释了蛋白质编码基因的3'非翻译区,并进行了微小RNA靶位点预测。聚焦于已知在该生物的伤口反应、后部模式形成和神经分化中起作用的基因,我们发现这些过程可能受到大量微小RNA的调控。值得注意的是,我们发现MIR-7和MIR-9家族中的微小RNA在后部基因的靶位点确实在动物的前部表达,这与对其相应靶基因的抑制作用一致。我们的注释为进一步的功能研究提供了候选微小RNA,为未来发育和再生过程中转录后控制的研究提供了资源。