Hu Jihong, Gui Songtao, Zhu Zhixuan, Wang Xiaolei, Ke Weidong, Ding Yi
State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, China.
Wuhan Vegetable Scientific Research Institute, Wuhan National Field Observation & Research Station for Aquatic Vegetables, Wuhan, 430065, China.
PLoS One. 2015 Nov 25;10(11):e0143765. doi: 10.1371/journal.pone.0143765. eCollection 2015.
Genomic resources such as single nucleotide polymorphism (SNPs), insertions and deletions (InDels) and SSRs (simple sequence repeats) are essential for crop improvement and better utilization in genetic breeding. However, the resources for the sacred lotus (Nelumbo nucifera Gaertn.) are still limited. In the present study, to dissect large-scale genomic molecular marker resources for sacred lotus, we re-sequenced a Thailand sacred lotus cultivar 'Chiang Mai wild lotus' and compared with the reported lotus genome 'Middle lake wild lotus'. A total of 3,180,059 SNPs, 328, 251 InDels and 14,191 SVs were found between the two genomes. The functional impact analyses of these SNPs indicated that they may be involved in metabolic processes, binding, catalytic activity, etc. Mining the genome sequences for SSRs showed that 191,657 SSRs were identified with a frequency of one SSR per 4.23 kb and 103,656 SSR primer pairs were designed. Furthermore, 14, 502 EST-SSRs were also indentified using the available RNA-seq data in the NCBI. A subset of 150 SSRs (genomic and EST-SSRs) was randomly selected for validation and genetic diversity analysis. The genotypes could be easily distinguished using these SSR markers and the 'Chiang Mai wild lotus' was obviously differentiated from the other Chinese accessions. This study provides considerable amounts of genomic resources and markers for the quantitative trait locus (QTL) identification and molecular selection of the species, which could have a potential role in various applications in sacred lotus breeding.
单核苷酸多态性(SNP)、插入缺失(InDel)和简单序列重复(SSR)等基因组资源对于作物改良和在遗传育种中的更好利用至关重要。然而,荷花(Nelumbo nucifera Gaertn.)的相关资源仍然有限。在本研究中,为了解析荷花大规模的基因组分子标记资源,我们对泰国荷花品种“清迈野生莲”进行了重测序,并与已报道的荷花基因组“中湖野生莲”进行比较。在这两个基因组之间共发现了3180059个SNP、328251个InDel和14191个结构变异(SV)。对这些SNP的功能影响分析表明,它们可能参与代谢过程、结合、催化活性等。对基因组序列进行SSR挖掘显示,共鉴定出191657个SSR,频率为每4.23 kb有一个SSR,并设计了103656对SSR引物对。此外,还利用NCBI中可用的RNA-seq数据鉴定出14502个EST-SSR。随机选择了150个SSR(基因组SSR和EST-SSR)子集进行验证和遗传多样性分析。使用这些SSR标记可以很容易地区分基因型,并且“清迈野生莲”与其他中国种质明显不同。本研究为该物种的数量性状基因座(QTL)鉴定和分子选择提供了大量的基因组资源和标记,这可能在荷花育种的各种应用中发挥潜在作用。