...
首页> 外文期刊>BMC Genomics >Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx
【24h】

Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx

机译:使用454 GSFlx对珊瑚幼虫转录组进行测序和从头分析

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Background New methods are needed for genomic-scale analysis of emerging model organisms that exemplify important biological questions but lack fully sequenced genomes. For example, there is an urgent need to understand the potential for corals to adapt to climate change, but few molecular resources are available for studying these processes in reef-building corals. To facilitate genomics studies in corals and other non-model systems, we describe methods for transcriptome sequencing using 454, as well as strategies for assembling a useful catalog of genes from the output. We have applied these methods to sequence the transcriptome of planulae larvae from the coral Acropora millepora. Results More than 600,000 reads produced in a single 454 sequencing run were assembled into ~40,000 contigs with five-fold average sequencing coverage. Based on sequence similarity with known proteins, these analyses identified ~11,000 different genes expressed in a range of conditions including thermal stress and settlement induction. Assembled sequences were annotated with gene names, conserved domains, and Gene Ontology terms. Targeted searches using these annotations identified the majority of genes associated with essential metabolic pathways and conserved signaling pathways, as well as novel candidate genes for stress-related processes. Comparisons with the genome of the anemone Nematostella vectensis revealed ~8,500 pairs of orthologs and ~100 candidate coral-specific genes. More than 30,000 SNPs were detected in the coral sequences, and a subset of these validated by re-sequencing. Conclusion The methods described here for deep sequencing of the transcriptome should be widely applicable to generate catalogs of genes and genetic markers in emerging model organisms. Our data provide the most comprehensive sequence resource currently available for reef-building corals, and include an extensive collection of potential genetic markers for association and population connectivity studies. The characterization of the larval transcriptome for this widely-studied coral will enable research into the biological processes underlying stress responses in corals and evolutionary adaptation to global climate change.
机译:背景技术对于新兴模型生物的基因组规模分析需要新的方法,这些方法例证了重要的生物学问题,但缺乏完整测序的基因组。例如,迫切需要了解珊瑚适应气候变化的潜力,但是很少有分子资源可用于研究造礁珊瑚的这些过程。为了促进在珊瑚和其他非模型系统中进行基因组学研究,我们描述了使用454进行转录组测序的方法,以及从输出结果中整理有用的基因目录的策略。我们已应用这些方法对来自珊瑚小球藻(Acropora millepora)的浮游幼虫的转录组进行测序。结果单次454测序运行中产生的600,000多个读数被组装成约40,000个重叠群,平均测序覆盖率为五倍。基于与已知蛋白质的序列相似性,这些分析确定了在包括热胁迫和沉降诱导在内的一系列条件下表达的约11,000种不同基因。组装的序列用基因名称,保守域和基因本体论术语标注。使用这些注释进行的有针对性的搜索确定了与基本代谢途径和保守的信号传导途径相关的大多数基因,以及与压力有关的过程的新候选基因。与海葵线虫Nematostella vectensis的基因组进行比较后,发现了约8,500对直系同源物和约100种候选珊瑚特异性基因。在珊瑚序列中检测到超过30,000个SNP,其中一部分通过重新测序得到验证。结论本文所述的转录组深度测序方法应可广泛用于在新兴模型生物中生成基因和遗传标记的目录。我们的数据提供了目前可用于建造珊瑚礁的珊瑚的最全面的序列资源,并且包括用于关联和种群连通性研究的大量潜在遗传标记。对这种被广泛研究的珊瑚的幼虫转录组的表征将使人们能够研究珊瑚中的应激反应以及对全球气候变化的进化适应所依据的生物学过程。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号