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为加速发展中国家的玉米改良而开发和部署高效的基因分型工作流程。

Developing and deploying an efficient genotyping workflow for accelerating maize improvement in developing countries.

作者信息

Offornedo Queen, Menkir Abebe, Babalola Deborah, Gedil Melaku

机构信息

Bioscience Center and Maize Improvement Program, International Institute of Tropical Agriculture (IITA) Headquarters, Ibadan, Oyo State, 200001, Nigeria.

出版信息

Gates Open Res. 2022 Aug 3;6:3. doi: 10.12688/gatesopenres.13338.3. eCollection 2022.

Abstract

Molecular breeding is an essential tool for accelerating genetic gain in crop improvement towards meeting the need to feed an ever-growing world population. Establishing low-cost, flexible genotyping platforms in small, public and regional laboratories can stimulate the application of molecular breeding in developing countries. These laboratories can serve plant breeding projects requiring low- to medium-density markers for marker-assisted selection (MAS) and quality control (QC) activities. We performed two QC and MAS experiments consisting of 637 maize lines, using an optimised genotyping workflow involving an in-house competitive allele-specific PCR (KASP) genotyping system with an optimised sample collection, preparation, and DNA extraction and quantitation process. A smaller volume of leaf-disc size plant samples was collected directly in 96-well plates for DNA extraction, using a slightly modified CTAB-based DArT DNA extraction protocol. DNA quality and quantity analyses were performed using a microplate reader, and the KASP genotyping and data analysis was performed in our laboratory. Applying the optimized genotyping workflow expedited the QC and MAS experiments from over five weeks (when outsourcing) to two weeks and eliminated the shipping cost. Using a set of 28 KASP single nucleotide polymorphisms (SNPs) validated for maize, the QC experiment revealed the genetic identity of four maize varieties taken from five seed sources. Another set of 10 KASP SNPs was sufficient in verifying the parentage of 390 F lines. The KASP-based MAS was successfully applied to a maize pro-vitamin A (PVA) breeding program and for introgressing the aflatoxin resistance gene into elite tropical maize lines. This improved workflow has helped accelerate maize improvement activities of IITA's Maize Improvement Program and facilitated DNA fingerprinting for tracking improved crop varieties. National Agricultural Research Systems (NARS) in developing countries can adopt this workflow to fast-track molecular marker-based genotyping for crop improvement.

摘要

分子育种是加速作物改良中遗传增益以满足养活不断增长的世界人口需求的重要工具。在小型、公共和区域实验室建立低成本、灵活的基因分型平台,可以促进分子育种在发展中国家的应用。这些实验室可以服务于需要低至中等密度标记进行标记辅助选择(MAS)和质量控制(QC)活动的植物育种项目。我们使用优化的基因分型工作流程,对637个玉米品系进行了两项QC和MAS实验,该工作流程包括一个内部竞争性等位基因特异性PCR(KASP)基因分型系统以及优化的样本采集、制备、DNA提取和定量过程。使用基于CTAB的DArT DNA提取方案的轻微修改版本,将较小体积的叶盘大小的植物样本直接收集到96孔板中用于DNA提取。使用酶标仪进行DNA质量和数量分析,并在我们实验室进行KASP基因分型和数据分析。应用优化的基因分型工作流程将QC和MAS实验从外包时的五周以上加快到两周,并消除了运输成本。使用一组经过玉米验证的28个KASP单核苷酸多态性(SNP),QC实验揭示了来自五个种子来源的四个玉米品种的遗传身份。另一组10个KASP SNP足以验证390个F代品系的亲本关系。基于KASP的MAS成功应用于玉米维生素A原(PVA)育种计划,并用于将黄曲霉毒素抗性基因导入优良热带玉米品系。这种改进的工作流程有助于加速国际热带农业研究所(IITA)玉米改良计划的玉米改良活动,并促进用于追踪改良作物品种的DNA指纹识别。发展中国家的国家农业研究系统(NARS)可以采用这种工作流程,快速推进基于分子标记的基因分型以进行作物改良。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b575/10313924/3aaecf806be9/gatesopenres-6-15059-g0000.jpg

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