Institute of Biotechnology, National Taiwan University, Taipei 106, Taiwan.
BMC Genomics. 2013 Jul 1;14:434. doi: 10.1186/1471-2164-14-434.
Salamanders are unique among vertebrates in their ability to completely regenerate amputated limbs through the mediation of blastema cells located at the stump ends. This regeneration is nerve-dependent because blastema formation and regeneration does not occur after limb denervation. To obtain the genomic information of blastema tissues, de novo transcriptomes from both blastema tissues and denervated stump ends of Ambystoma mexicanum (axolotls) 14 days post-amputation were sequenced and compared using Solexa DNA sequencing.
The sequencing done for this study produced 40,688,892 reads that were assembled into 307,345 transcribed sequences. The N50 of transcribed sequence length was 562 bases. A similarity search with known proteins identified 39,200 different genes to be expressed during limb regeneration with a cut-off E-value exceeding 10-5. We annotated assembled sequences by using gene descriptions, gene ontology, and clusters of orthologous group terms. Targeted searches using these annotations showed that the majority of the genes were in the categories of essential metabolic pathways, transcription factors and conserved signaling pathways, and novel candidate genes for regenerative processes. We discovered and confirmed numerous sequences of the candidate genes by using quantitative polymerase chain reaction and in situ hybridization.
The results of this study demonstrate that de novo transcriptome sequencing allows gene expression analysis in a species lacking genome information and provides the most comprehensive mRNA sequence resources for axolotls. The characterization of the axolotl transcriptome can help elucidate the molecular mechanisms underlying blastema formation during limb regeneration.
蝾螈在脊椎动物中具有独特的能力,能够通过位于残端的芽基细胞的介导完全再生截肢的肢体。这种再生是依赖神经的,因为在肢体去神经后,芽基的形成和再生不会发生。为了获得芽基组织的基因组信息,对 14 天截肢后 Ambystoma mexicanum(墨西哥蝾螈)的芽基组织和去神经残端的从头转录组进行了测序,并使用 Solexa DNA 测序进行了比较。
本研究的测序产生了 40,688,892 个读数,这些读数被组装成 307,345 个转录序列。转录序列长度的 N50 为 562 个碱基。与已知蛋白的相似性搜索确定了在肢体再生过程中表达的 39,200 个不同基因,截止 E 值超过 10-5。我们通过基因描述、基因本体和同源基因簇术语对组装序列进行了注释。使用这些注释进行的靶向搜索表明,大多数基因属于必需代谢途径、转录因子和保守信号通路的类别,以及再生过程的新候选基因。我们通过定量聚合酶链反应和原位杂交发现并证实了许多候选基因的序列。
本研究的结果表明,从头转录组测序允许在缺乏基因组信息的物种中进行基因表达分析,并为墨西哥蝾螈提供了最全面的 mRNA 序列资源。对墨西哥蝾螈转录组的特征描述有助于阐明肢体再生过程中芽基形成的分子机制。