Kayam Galya, Brand Yael, Faigenboim-Doron Adi, Patil Abhinandan, Hedvat Ilan, Hovav Ran
Department of Field Crops, Plant Science Institute, Agricultural Research OrganizationBet-Dagan, Israel.
Front Plant Sci. 2017 Apr 4;8:467. doi: 10.3389/fpls.2017.00467. eCollection 2017.
The growth habit of lateral shoots (also termed "branching habit") is an important descriptive and agronomic character of peanut. Yet, both the inheritance of branching habit and the genetic mechanism that controls it in this crop remain unclear. In addition, the low degree of polymorphism among cultivated peanut varieties hinders fine-mapping of this and other traits in non-homozygous genetic structures. Here, we combined high-throughput sequencing with a well-defined genetic system to study these issues in peanut. Initially, segregating F populations derived from a reciprocal cross between very closely related Virginia-type peanut cultivars with spreading and bunch growth habits were examined. The spreading/bunch trait was shown to be controlled by a single gene with no cytoplasmic effect. That gene was named and was significantly correlated with pod yield per plant, time to maturation and the ratio of "dead-end" pods. Subsequently, bulked segregant analysis was performed on 52 completely bunch, and 47 completely spreading F families. In order to facilitate the process of SNP detection and candidate-gene analysis, the transcriptome was used instead of genomic DNA. Young leaves were sampled and bulked. Reads from Illumina sequencing were aligned against the peanut reference transcriptome and the diploid genomes. Inter-varietal SNPs were detected, scored and quality-filtered. Thirty-four candidate SNPs were found to have a bulk frequency ratio value >10 and 6 of those SNPs were found to be located in the genomic region of linkage group B5. Three best hits from that over-represented region were further analyzed in the segregating population. The trait locus was found to be located in a ~1.1 Mbp segment between markers M875 (B5:145,553,897; 1.9 cM) and M255 (B5:146,649,943; 2.25 cM). The method was validated using a population of recombinant inbreed lines of the same cross and a new DNA SNP-array. This study demonstrates the relatively straight-forward utilization of bulk segregant analysis for trait fine-mapping in the low polymeric and heterozygous germplasm of cultivated peanut and provides a baseline for candidate gene discovery and map-based cloning of .
侧枝的生长习性(也称为“分枝习性”)是花生的一个重要描述性和农艺性状。然而,花生中分枝习性的遗传以及控制它的遗传机制仍不清楚。此外,栽培花生品种间多态性程度较低,阻碍了在非纯合遗传结构中对该性状及其他性状的精细定位。在此,我们将高通量测序与明确的遗传系统相结合,以研究花生中的这些问题。最初,对源自具有蔓生和丛生生长习性的亲缘关系非常近的弗吉尼亚型花生品种间正反交产生的分离F群体进行了研究。蔓生/丛生性状显示由一个单基因控制,无细胞质效应。该基因被命名为 ,并且与单株荚果产量、成熟时间和“无果荚”比例显著相关。随后,对52个完全丛生和47个完全蔓生的F家系进行了混合分离分析。为了便于单核苷酸多态性(SNP)检测和候选基因分析过程,使用转录组而非基因组DNA。采集幼叶并混合。将来自Illumina测序的读数与花生参考转录组和二倍体基因组进行比对。检测、评分并对品种间SNP进行质量过滤。发现34个候选SNP的混合频率比值>10,其中6个SNP位于连锁群B5的基因组区域。在分离群体中进一步分析了该过度代表区域的三个最佳命中位点。发现性状位点位于标记M875(B5:145,553,897;1.9厘摩)和M255(B5:146,649,943;2.25厘摩)之间约1.1兆碱基对的区段。使用相同杂交组合的重组自交系群体和新的DNA SNP阵列对该方法进行了验证。本研究证明了在栽培花生的低聚合和杂合种质中,混合分离分析用于性状精细定位相对简便,并为候选基因发现和基于图谱的 克隆提供了基线。