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方法:-:一种用于水稻标记辅助选择的基于单种子的抽样策略。

Methodology: -: a single seed-based sampling strategy for marker-assisted selection in rice.

作者信息

Arbelaez Juan David, Tandayu Erwin, Reveche Maria Ymber, Jarana Annalhea, van Rogen Petra, Sandager Line, Stolt Patrik, Ng Enghwa, Varshney Rajeev K, Kretzschmar Tobias, Cobb Joshua

机构信息

1International Rice Research Institute, Metro Manila, DAPO Box 7777, Los Baños, 1301 Philippines.

Intertek - AgriTech, 2-230-53 Alnarp, Elevenborgsvägen Sweden.

出版信息

Plant Methods. 2019 Jul 24;15:78. doi: 10.1186/s13007-019-0464-2. eCollection 2019.

Abstract

BACKGROUND

Integrated breeding approaches such as combining marker-assisted selection and rapid line fixation through single-seed-descent, can effectively increase the frequency of desirable alleles in a breeding program and increase the rate of genetic gain for quantitative traits by shortening the breeding cycle. However, with most genotyping being outsourced to 3rd party service providers' nowadays, sampling has become the bottleneck for many breeding programs. While seed-chipping as prevailed as an automatable seed sampling protocol in many species, the symmetry of rice seeds makes this solution as laborious and costly as sampling leaf tissue. The aim of this study is to develop, validate and deploy a single seed sampling strategy for marker-assisted selection of fixed lines in rice that is more efficient, cost-effective and convenient compared to leaf-based sampling protocols without compromising the accuracy of the marker-assisted selection results.

RESULTS

Evaluations replicated across accessions and markers showed that a single rice seed is sufficient to generate enough DNA (7-8 ng/μL) to run at least ten PCR trait-markers suitable for marker-assisted selection strategies in rice. The DNA quantity and quality extracted from single seeds from fixed lines (F) with different physical and/or chemical properties were not significantly different. Nor were there significant differences between single seeds collected 15 days after panicle initiation compared to those harvested at maturity. A large-scale comparison between single seed and leaf-based methodologies showed not only high levels of genotypic concordance between both protocols (~ 99%) but also higher SNP call rates in single seed (99.24% vs. 97.5% in leaf). A cost-benefit analysis showed that this single seed sampling strategy decreased the cost of sampling fourfold. An advantage of this approach is that desirable genotypes can be selected before investing in planting activities reducing the cost associated with field operations.

CONCLUSION

This study reports the development of a cost-effective and simple single seed genotyping strategy that facilitates the adoption and deployment of marker-assisted selection strategies in rice. This will allow breeders to increase the frequency of favorable alleles and combine rapid generation advancement techniques much more cost-effectively accelerating the process and efficiency of parental selection and varietal development.

摘要

背景

诸如将标记辅助选择与通过单粒传进行快速株系固定相结合的综合育种方法,能够有效提高育种计划中优良等位基因的频率,并通过缩短育种周期提高数量性状的遗传增益速率。然而,如今大多数基因分型工作都外包给了第三方服务提供商,采样已成为许多育种计划的瓶颈。虽然种子破碎作为一种可自动化的种子采样方案在许多物种中很普遍,但水稻种子的对称性使得这种方法与采样叶片组织一样费力且成本高昂。本研究的目的是开发、验证和应用一种用于水稻固定株系标记辅助选择的单粒种子采样策略,该策略比基于叶片的采样方案更高效、更具成本效益且更方便,同时不影响标记辅助选择结果的准确性。

结果

在不同种质和标记间进行的重复评估表明,一粒水稻种子足以产生足够的DNA(7 - 8 ng/μL),以运行至少十个适合水稻标记辅助选择策略的PCR性状标记。从具有不同物理和/或化学特性的固定株系(F)的单粒种子中提取的DNA数量和质量没有显著差异。与成熟时收获的种子相比,在穗分化开始15天后收集的单粒种子之间也没有显著差异。单粒种子和基于叶片的方法之间的大规模比较表明,两种方案之间不仅具有高水平的基因型一致性(约99%),而且单粒种子中的SNP检出率更高(99.24%对叶片中的97.5%)。成本效益分析表明,这种单粒种子采样策略将采样成本降低了四倍。这种方法的一个优点是,可以在投入种植活动之前选择理想的基因型,从而降低与田间操作相关的成本。

结论

本研究报告了一种具有成本效益且简单的单粒种子基因分型策略的开发,该策略有助于在水稻中采用和应用标记辅助选择策略。这将使育种者能够更经济高效地提高有利等位基因的频率,并结合快速世代推进技术,加速亲本选择和品种开发的过程和效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47af/6652012/af870dc87999/13007_2019_464_Fig1_HTML.jpg

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