Xu Sen, Ackerman Matthew S, Long Hongan, Bright Lydia, Spitze Ken, Ramsdell Jordan S, Thomas W Kelley, Lynch Michael
Department of Biology, Indiana University, Bloomington, Indiana 47405
Department of Biology, Indiana University, Bloomington, Indiana 47405.
Genetics. 2015 Sep;201(1):31-8. doi: 10.1534/genetics.115.179028. Epub 2015 Jun 26.
Genetic linkage maps are critical for assembling draft genomes to a meaningful chromosome level and for deciphering the genomic underpinnings of biological traits. The estimates of recombination rates derived from genetic maps also play an important role in understanding multiple aspects of genomic evolution such as nucleotide substitution patterns and accumulation of deleterious mutations. In this study, we developed a high-throughput experimental approach that combines fluorescence-activated cell sorting, whole-genome amplification, and short-read sequencing to construct a genetic map using single-sperm cells. Furthermore, a computational algorithm was developed to analyze single-sperm whole-genome sequencing data for map construction. These methods allowed us to rapidly build a male-specific genetic map for the freshwater microcrustacean Daphnia pulex, which shows significant improvements compared to a previous map. With a total of mapped 1672 haplotype blocks and an average intermarker distance of 0.87 cM, this map spans a total genetic distance of 1451 Kosambi cM and comprises 90% of the resolved regions in the current Daphnia reference assembly. The map also reveals the mistaken mapping of seven scaffolds in the reference assembly onto chromosome II by a previous microsatellite map based on F2 crosses. Our approach can be easily applied to many other organisms and holds great promise for unveiling the intragenomic and intraspecific variation in the recombination rates.
遗传连锁图谱对于将基因组草图组装到有意义的染色体水平以及解读生物性状的基因组基础至关重要。从遗传图谱得出的重组率估计值在理解基因组进化的多个方面(如核苷酸替换模式和有害突变的积累)中也起着重要作用。在本研究中,我们开发了一种高通量实验方法,该方法结合了荧光激活细胞分选、全基因组扩增和短读长测序,以使用单精子细胞构建遗传图谱。此外,还开发了一种计算算法来分析单精子全基因组测序数据以进行图谱构建。这些方法使我们能够快速构建淡水微型甲壳动物水蚤的雄性特异性遗传图谱,与之前的图谱相比有显著改进。该图谱共定位了1672个单倍型块,标记间平均距离为0.87厘摩,总遗传距离为1451个科桑比厘摩,涵盖了当前水蚤参考组装中90%的解析区域。该图谱还揭示了基于F2杂交的先前微卫星图谱将参考组装中的7个支架错误映射到了二号染色体上。我们的方法可以很容易地应用于许多其他生物体,并有望揭示重组率的基因组内和种内变异。