ICAR-Central Research Institute for Jute and Allied Fibres, Barrackpore, Kolkata, 700121, India.
School of Agriculture and Rural Development, Ramakrishna Mission Vivekananda University, Ramakrishna Mission Ashrama, Narendrapur, Kolkata, 700103, India.
J Appl Genet. 2019 Feb;60(1):13-25. doi: 10.1007/s13353-018-0476-z. Epub 2018 Oct 27.
We designed a set of 580 simple sequence repeat markers; 506 from transcription factor-coding genes, and 74 from long non-coding RNAs and designated them as regulatory gene-derived simple sequence repeat (ReG-SSR) markers. From this set, we could anchor 559 ReG-SSR markers on 15 flax chromosomes with an average marker distance of 0.56 Mb. Thirty-one polymorphic ReG-SSR primers, amplifying SSR loci length of at least 20 bp were chosen from 134 screened primers. This primer set was used to characterize a diversity panel of 93 flax accessions. The panel included 33 accessions from India, including released varieties, dual-purpose lines and landraces, and 60 fiber flax accessions from the global core collection. Thirty-one ReG-SSR markers generated 76 alleles, with an average of 2.5 alleles per primer and a mean allele frequency of 0.77. These markers recorded 0.32 average gene diversity, 0.26 polymorphism information content and 1.35% null alleles. All the 31 ReG-SSR loci were found selectively neutral and showed no evidence of population reduction. A model-based clustering analysis separated the flax accessions into two sub-populations-Indian and global, with some accessions showing admixtures. The distinct clustering pattern of the Indian accessions compared to the global accessions, conforms to the principal coordinate analysis, genetic dissimilarity-based unweighted neighbor-joining tree and analysis of molecular variance. Fourteen flax accessions with 99.3% allelic richness were found optimum to adopt in breeding programs. In summary, the genome-wide ReG-SSR markers will serve as a functional marker resource for genetic and phenotypic relationship studies, marker-assisted selections, and provide a basis for selection of accessions from the Indian and global gene pool in fiber flax breeding programs.
我们设计了一套 580 个简单重复序列标记;其中 506 个来自转录因子编码基因,74 个来自长非编码 RNA,并将其命名为调节基因衍生简单重复序列(ReG-SSR)标记。从这组标记中,我们可以将 559 个 ReG-SSR 标记锚定在 15 个亚麻染色体上,平均标记间距为 0.56 Mb。从 134 个筛选出的引物中,选择了 31 个扩增 SSR 位点长度至少为 20 bp 的多态性 ReG-SSR 引物。该引物组用于对 93 个亚麻品系的多样性面板进行特征分析。该面板包括来自印度的 33 个品系,包括已发布的品种、两用系和地方品种,以及来自全球核心收集的 60 个纤维亚麻品系。31 个 ReG-SSR 标记产生了 76 个等位基因,每个引物平均产生 2.5 个等位基因,平均等位基因频率为 0.77。这些标记记录了 0.32 的平均基因多样性、0.26 的多态信息含量和 1.35%的无效等位基因。所有 31 个 ReG-SSR 位点均被发现为选择中性,且没有种群减少的证据。基于模型的聚类分析将亚麻品系分为两个亚群——印度和全球,其中一些品系显示出混合。与全球品系相比,印度品系的明显聚类模式符合主坐标分析、基于遗传距离的非加权邻接法树和分析分子方差。发现 14 个具有 99.3%等位基因丰富度的亚麻品系是最佳的在育种计划中采用。总之,全基因组 ReG-SSR 标记将作为遗传和表型关系研究、标记辅助选择的功能标记资源,并为纤维亚麻育种计划中从印度和全球基因库中选择品系提供基础。