Chou Hsien-Chao, Pruitt Margaret M, Bastin Benjamin R, Schneider Stephan Q
Department of Genetics, Development and Cell Biology, Iowa State University, 503 Science Hall II, Ames, IA, 50011, USA.
Present Address: National Cancer Institute, US National Institutes of Health, Bethesda, Maryland, USA.
BMC Genomics. 2016 Aug 5;17:552. doi: 10.1186/s12864-016-2860-6.
The spiral cleavage mode of early development is utilized in over one-third of all animal phyla and generates embryonic cells of different size, position, and fate through a conserved set of stereotypic and invariant asymmetric cell divisions. Despite the widespread use of spiral cleavage, regulatory and molecular features for any spiral-cleaving embryo are largely uncharted. To address this gap we use RNA-sequencing on the spiralian model Platynereis dumerilii to capture and quantify the first complete genome-wide transcriptional landscape of early spiral cleavage.
RNA-sequencing datasets from seven stages in early Platynereis development, from the zygote to the protrochophore, are described here including the de novo assembly and annotation of ~17,200 Platynereis genes. Depth and quality of the RNA-sequencing datasets allow the identification of the temporal onset and level of transcription for each annotated gene, even if the expression is restricted to a single cell. Over 4000 transcripts are maternally contributed and cleared by the end of the early spiral cleavage phase. Small early waves of zygotic expression are followed by major waves of thousands of genes, demarcating the maternal to zygotic transition shortly after the completion of spiral cleavages in this annelid species.
Our comprehensive stage-specific transcriptional analysis of early embryonic stages in Platynereis elucidates the regulatory genome during early spiral embryogenesis and defines the maternal to zygotic transition in Platynereis embryos. This transcriptome assembly provides the first systems-level view of the transcriptional and regulatory landscape for a spiral-cleaving embryo.
超过三分之一的动物门在早期发育过程中采用螺旋卵裂模式,通过一组保守的定型且不变的不对称细胞分裂产生大小、位置和命运各异的胚胎细胞。尽管螺旋卵裂被广泛应用,然而任何螺旋卵裂胚胎的调控和分子特征在很大程度上仍未被探索。为填补这一空白,我们对螺旋动物模型杜氏阔沙蚕进行RNA测序,以捕获和量化早期螺旋卵裂首个完整的全基因组转录图谱。
本文描述了杜氏阔沙蚕早期发育从合子到原担轮幼虫七个阶段的RNA测序数据集,包括约17200个杜氏阔沙蚕基因的从头组装和注释。RNA测序数据集的深度和质量使得即便某个基因的表达仅限于单个细胞,也能鉴定出每个注释基因转录的时间起始点和水平。超过4000个转录本由母体提供,并在早期螺旋卵裂阶段结束时清除。合子表达的早期小波动之后是数千个基因的主要波动,这在该环节动物物种螺旋卵裂完成后不久就界定了母体向合子的转变。
我们对杜氏阔沙蚕早期胚胎阶段进行的全面的阶段特异性转录分析阐明了早期螺旋胚胎发生过程中的调控基因组,并定义了杜氏阔沙蚕胚胎中母体向合子的转变。这个转录组组装提供了首个关于螺旋卵裂胚胎转录和调控图谱的系统水平视图。