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一种用于检测四倍体和六倍体小麦中诱导突变的改良定向诱导基因组局部突变技术方法。

A modified TILLING approach to detect induced mutations in tetraploid and hexaploid wheat.

作者信息

Uauy Cristobal, Paraiso Francine, Colasuonno Pasqualina, Tran Robert K, Tsai Helen, Berardi Steve, Comai Luca, Dubcovsky Jorge

机构信息

Department of Plant Sciences, University of California, Davis, CA 95616, USA.

出版信息

BMC Plant Biol. 2009 Aug 28;9:115. doi: 10.1186/1471-2229-9-115.

Abstract

BACKGROUND

Wheat (Triticum ssp.) is an important food source for humans in many regions around the world. However, the ability to understand and modify gene function for crop improvement is hindered by the lack of available genomic resources. TILLING is a powerful reverse genetics approach that combines chemical mutagenesis with a high-throughput screen for mutations. Wheat is specially well-suited for TILLING due to the high mutation densities tolerated by polyploids, which allow for very efficient screens. Despite this, few TILLING populations are currently available. In addition, current TILLING screening protocols require high-throughput genotyping platforms, limiting their use.

RESULTS

We developed mutant populations of pasta and common wheat and organized them for TILLING. To simplify and decrease costs, we developed a non-denaturing polyacrylamide gel set-up that uses ethidium bromide to detect fragments generated by crude celery juice extract digestion of heteroduplexes. This detection method had similar sensitivity as traditional LI-COR screens, suggesting that it represents a valid alternative. We developed genome-specific primers to circumvent the presence of multiple homoeologous copies of our target genes. Each mutant library was characterized by TILLING multiple genes, revealing high mutation densities in both the hexaploid (1/38 kb) and tetraploid (1/51 kb) populations for 50% GC targets. These mutation frequencies predict that screening 1,536 lines for an effective target region of 1.3 kb with 50% GC content will result in ~52 hexaploid and ~39 tetraploid mutant alleles. This implies a high probability of obtaining knock-out alleles (P = 0.91 for hexaploid, P = 0.84 for tetraploid), in addition to multiple missense mutations. In total, we identified over 275 novel alleles in eleven targeted gene/genome combinations in hexaploid and tetraploid wheat and have validated the presence of a subset of them in our seed stock.

CONCLUSION

We have generated reverse genetics TILLING resources for pasta and bread wheat and achieved a high mutation density in both populations. We also developed a modified screening method that will lower barriers to adopt this promising technology. We hope that the use of this reverse genetics resource will enable more researchers to pursue wheat functional genomics and provide novel allelic diversity for wheat improvement.

摘要

背景

小麦(Triticum ssp.)是世界上许多地区人类重要的食物来源。然而,由于缺乏可用的基因组资源,了解和修改基因功能以改良作物的能力受到阻碍。定向诱导基因组局部突变(TILLING)是一种强大的反向遗传学方法,它将化学诱变与高通量突变筛选相结合。由于多倍体能够耐受高突变密度,这使得小麦特别适合进行TILLING,从而实现非常高效的筛选。尽管如此,目前可用的TILLING群体很少。此外,当前的TILLING筛选方案需要高通量基因分型平台,限制了它们的应用。

结果

我们开发了硬粒小麦和普通小麦的突变群体,并将它们组织起来用于TILLING。为了简化并降低成本,我们开发了一种非变性聚丙烯酰胺凝胶装置,该装置使用溴化乙锭来检测由粗制芹菜汁提取物消化异源双链体产生的片段。这种检测方法具有与传统LI-COR筛选相似的灵敏度,表明它是一种有效的替代方法。我们开发了基因组特异性引物,以规避目标基因多个同源拷贝的存在。每个突变体文库通过TILLING多个基因进行表征,结果显示对于50% GC含量的目标,六倍体(约1/38 kb)和四倍体(约1/51 kb)群体中的突变密度都很高。这些突变频率预测,对于1.3 kb的有效目标区域且GC含量为50%,筛选1536个株系将在六倍体中产生约52个突变等位基因,在四倍体中产生约39个突变等位基因。这意味着除了多个错义突变外,获得敲除等位基因的概率很高(六倍体中P = 0.91,四倍体中P = 0.84)。我们总共在六倍体和四倍体小麦的十一种靶向基因/基因组组合中鉴定出超过275个新等位基因,并已在我们的种子库中验证其中一部分的存在。

结论

我们为硬粒小麦和面包小麦生成了反向遗传学TILLING资源,并在两个群体中都实现了高突变密度。我们还开发了一种改进的筛选方法,这将降低采用这项有前景技术的障碍。我们希望这种反向遗传学资源的使用将使更多研究人员能够开展小麦功能基因组学研究,并为小麦改良提供新的等位基因多样性。

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