Genome Research Center, NODAI Research Institute, Tokyo University of Agriculture, Setagaya-ku, Tokyo, Japan.
PLoS One. 2011;6(10):e26043. doi: 10.1371/journal.pone.0026043. Epub 2011 Oct 10.
While the study of phenotypic variation is a central theme in evolutionary biology, the genetic approaches available to understanding this variation are usually limited because of a lack of genomic information in non-model organisms. This study explored the utility of next-generation sequencing (NGS) technologies for studying phenotypic variations between 2 populations of a non-model species, the Hokkai shrimp (Pandalus latirostris; Decapoda, Pandalidae). Before we performed transcriptome analyses using NGS, we examined the genetic and phenotypic differentiation between the populations. Analyses using microsatellite DNA markers suggested that these populations genetically differed from one another and that gene flow is restricted between them. Moreover, the results of our 4-year field observations indicated that the egg traits varied genetically between the populations. Using mRNA extracted from the ovaries of 5 females in each population of Hokkai shrimp, we then performed a transcriptome analysis of the 2 populations. A total of 13.66 gigabases (Gb) of 75-bp reads was obtained. Further, 58,804 and 33,548 contigs for the first and second population, respectively, and 47,467 contigs for both populations were produced by de novo assembly. We detected 552 sequences with the former approach and 702 sequences with the later one; both sets of sequences showed greater than twofold differences in the expression levels between the 2 populations. Twenty-nine sequences were found in both approaches and were considered to be differentially expressed genes. Among them, 9 sequences showed significant similarity to functional genes. The present study showed a de novo assembly approach for the transcriptome of a non-model species using only short-read sequence data, and provides a strategy for identifying sequences showing significantly different expression levels between populations.
虽然表型变异的研究是进化生物学的一个核心主题,但由于缺乏非模式生物的基因组信息,用于理解这种变异的遗传方法通常受到限制。本研究探讨了下一代测序(NGS)技术在研究非模式物种——北海道虾(Pandalus latirostris;十足目,对虾科)两个种群之间表型变异中的应用。在使用 NGS 进行转录组分析之前,我们先检查了种群之间的遗传和表型分化。微卫星 DNA 标记分析表明,这些种群在遗传上彼此不同,基因流受到限制。此外,我们 4 年的野外观察结果表明,种群之间的卵特征存在遗传差异。我们从北海道虾的每个种群的 5 只雌虾的卵巢中提取 mRNA,然后对这两个种群进行转录组分析。共获得了 13.66 吉字节(Gb)的 75-bp 读段。进一步地,分别对第一个和第二个种群进行从头组装,得到了 58804 和 33548 条 contigs,两个种群共有 47467 条 contigs。我们用前一种方法检测到 552 个序列,用后一种方法检测到 702 个序列;两组序列在两个种群之间的表达水平差异均大于两倍。在两种方法中都发现了 29 个序列,被认为是差异表达基因。其中,9 个序列与功能基因具有显著相似性。本研究展示了一种仅使用短读序列数据对非模式物种的转录组进行从头组装的方法,并提供了一种用于识别种群间表达水平差异显著的序列的策略。