Blanc-Mathieu Romain, Verhelst Bram, Derelle Evelyne, Rombauts Stephane, Bouget François-Yves, Carré Isabelle, Château Annie, Eyre-Walker Adam, Grimsley Nigel, Moreau Hervé, Piégu Benoit, Rivals Eric, Schackwitz Wendy, Van de Peer Yves, Piganeau Gwenaël
CNRS, UMR 7232, Observatoire Océanologique, Avenue du Fontaulé, BP44, 66650 Banyuls-sur-Mer, France.
BMC Genomics. 2014 Dec 13;15(1):1103. doi: 10.1186/1471-2164-15-1103.
Cost effective next generation sequencing technologies now enable the production of genomic datasets for many novel planktonic eukaryotes, representing an understudied reservoir of genetic diversity. O. tauri is the smallest free-living photosynthetic eukaryote known to date, a coccoid green alga that was first isolated in 1995 in a lagoon by the Mediterranean sea. Its simple features, ease of culture and the sequencing of its 13 Mb haploid nuclear genome have promoted this microalga as a new model organism for cell biology. Here, we investigated the quality of genome assemblies of Illumina GAIIx 75 bp paired-end reads from Ostreococcus tauri, thereby also improving the existing assembly and showing the genome to be stably maintained in culture.
The 3 assemblers used, ABySS, CLCBio and Velvet, produced 95% complete genomes in 1402 to 2080 scaffolds with a very low rate of misassembly. Reciprocally, these assemblies improved the original genome assembly by filling in 930 gaps. Combined with additional analysis of raw reads and PCR sequencing effort, 1194 gaps have been solved in total adding up to 460 kb of sequence. Mapping of RNAseq Illumina data on this updated genome led to a twofold reduction in the proportion of multi-exon protein coding genes, representing 19% of the total 7699 protein coding genes. The comparison of the DNA extracted in 2001 and 2009 revealed the fixation of 8 single nucleotide substitutions and 2 deletions during the approximately 6000 generations in the lab. The deletions either knocked out or truncated two predicted transmembrane proteins, including a glutamate-receptor like gene.
High coverage (>80 fold) paired-end Illumina sequencing enables a high quality 95% complete genome assembly of a compact ~13 Mb haploid eukaryote. This genome sequence has remained stable for 6000 generations of lab culture.
具有成本效益的新一代测序技术现在能够为许多新型浮游真核生物生成基因组数据集,这些真核生物代表了一个尚未得到充分研究的遗传多样性库。莱茵衣藻是迄今为止已知的最小的自由生活光合真核生物,是一种球状绿藻,于1995年首次在地中海的一个泻湖中分离出来。它的简单特征、易于培养以及其13 Mb单倍体核基因组的测序,使这种微藻成为细胞生物学的一种新的模式生物。在这里,我们研究了来自莱茵衣藻的Illumina GAIIx 75 bp双末端读段的基因组组装质量,从而改进了现有的组装,并表明该基因组在培养中能稳定维持。
所使用的3种组装程序ABySS、CLCBio和Velvet,在1402至2080个支架中产生了95%完整的基因组,错误组装率非常低。相反,这些组装通过填补930个缺口改进了原始基因组组装。结合对原始读段的额外分析和PCR测序工作,总共解决了1194个缺口,增加了460 kb的序列。将RNAseq Illumina数据映射到这个更新的基因组上,导致多外显子蛋白质编码基因的比例降低了两倍,占总共7699个蛋白质编码基因的19%。对2001年和2009年提取的DNA的比较显示,在实验室大约6000代中固定了8个单核苷酸替换和2个缺失。这些缺失要么敲除要么截断了两个预测的跨膜蛋白,包括一个类谷氨酸受体基因。
高覆盖率(>80倍)的双末端Illumina测序能够对一个紧凑的约13 Mb单倍体真核生物进行高质量的95%完整基因组组装。这个基因组序列在实验室培养的6000代中一直保持稳定。