Division of Plant Sciences and Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Funct Integr Genomics. 2011 Dec;11(4):539-49. doi: 10.1007/s10142-011-0225-4. Epub 2011 May 4.
To test the function of candidate genes in soybean for resistance to the soybean cyst nematode (SCN), a large collection of EMS-mutants from the SCN-resistant soybean cultivar "Forrest" was developed for Targeting Induced Local Lesions IN Genomes (TILLING). Additionally, due to the complexity of the soybean genome, an integrated set of genomic and genetic analysis tools was employed to complement the TILLING approach. The efficiency of this integrated set of tools was tested using a candidate soybean gene for resistance to SCN, encoding a leucine-rich repeat receptor-like kinase (LRR-RLK) that was identified by map-based cloning at the Rhg4 locus. The Rhg4 locus is one of the major quantitative trait loci controlling soybean resistance against SCN race 3 (HG type 0) in cv. Forrest, but the gene(s) sequence for resistance remains to be determined. Using TILLING, a Forrest mutant containing a nonsense mutation in the LRR domain of the candidate resistance protein was identified and confirmed; however, the SCN-resistant phenotype of the mutant was not altered. Haplotyping and EcoTILLING of recombinant inbred lines along with complementation analysis corroborated the TILLING result and ruled out the possibility of functional redundancy by a second copy of the LRR-RLK gene identified in the soybean genome. This study validates the use of TILLING, in combination with an integrated set of genomic tools, as an efficient means of testing candidate genes for SCN resistance in soybean.
为了测试大豆抗大豆胞囊线虫(SCN)候选基因的功能,从抗 SCN 的大豆品种“Forrest”中开发了大量 EMS 突变体,用于靶向诱导基因组局部突变(TILLING)。此外,由于大豆基因组的复杂性,采用了一套综合的基因组和遗传分析工具来补充 TILLING 方法。通过基于图谱克隆在 Rhg4 基因座上鉴定的编码富含亮氨酸重复受体样激酶(LRR-RLK)的候选大豆抗 SCN 基因,测试了这套综合工具的效率。Rhg4 基因座是控制 Forrest 品种抗 SCN 第 3 号(HG 型 0)的主要数量性状基因座之一,但抗基因序列仍有待确定。使用 TILLING,鉴定并证实了 Forrest 突变体中候选抗性蛋白 LRR 结构域存在无义突变;然而,突变体的抗 SCN 表型并未改变。重组自交系的单倍型分析和 EcoTILLING 以及互补分析证实了 TILLING 结果,并排除了大豆基因组中鉴定的第二个 LRR-RLK 基因的功能冗余的可能性。这项研究验证了 TILLING 与一套综合基因组工具相结合,作为测试大豆抗 SCN 候选基因的有效方法。