Department of Agronomy, Purdue University, 915 W State Street, West Lafayette, IN 47907-2054, USA.
Theor Appl Genet. 2012 Apr;124(6):989-1003. doi: 10.1007/s00122-011-1763-9. Epub 2011 Dec 13.
Striga is a devastating parasitic weed in Africa and parts of Asia. Low Striga germination stimulant activity, a well-known resistance mechanism in sorghum, is controlled by a single recessive gene (lgs). Molecular markers linked to the lgs gene can accelerate development of Striga-resistant cultivars. Using a high density linkage map constructed with 367 markers (DArT and SSRs) and an in vitro assay for germination stimulant activity towards Striga asiatica in 354 recombinant inbred lines derived from SRN39 (low stimulant) × Shanqui Red (high stimulant), we precisely tagged and mapped the lgs gene on SBI-05 between two tightly linked microsatellite markers SB3344 and SB3352 at a distance of 0.5 and 1.5 cM, respectively. The fine-mapped lgs region was delimited to a 5.8 cM interval with the closest three markers SB3344, SB3346 and SB3343 positioned at 0.5, 0.7 and 0.9 cM, respectively. We validated tightly linked markers in a set of 23 diverse sorghum accessions, most of which were known to be Striga resistant, by genotyping and phenotyping for germination stimulant activity towards both S. asiatica and S. hermonthica. The markers co-segregated with Striga germination stimulant activity in 21 of the 23 tested lines. The lgs locus similarly affected germination stimulant activity for both Striga species. The identified markers would be useful in marker-assisted selection for introgressing this trait into susceptible sorghum cultivars. Examination of the sorghum genome sequence and comparative analysis with the rice genome suggests some candidate genes in the fine-mapped region (400 kb) that may affect strigolactone biosynthesis or exudation. This work should form a foundation for map-based cloning of the lgs gene and aid in elucidation of an exact mechanism for resistance based on low Striga germination stimulant activity.
独脚金是一种在非洲和亚洲部分地区具有破坏性的寄生杂草。低独脚金发芽刺激素活性是高粱中一种已知的抗性机制,由单个隐性基因(lgs)控制。与 lgs 基因连锁的分子标记可加速抗独脚金品种的开发。本研究使用由 367 个标记(DArT 和 SSRs)构建的高密度连锁图谱和 354 个来自 SRN39(低刺激素)×Shanqui Red(高刺激素)的重组自交系的体外独脚金亚洲种发芽刺激素活性测定,在 SRN39(低刺激素)×Shanqui Red(高刺激素)的 354 个重组自交系中,我们在 SBI-05 上精确标记和映射了 lgs 基因,该基因位于两个紧密连锁的微卫星标记 SB3344 和 SB3352 之间,距离分别为 0.5 和 1.5cM。精细定位的 lgs 区域被限定在一个 5.8cM 的区间内,最近的三个标记 SB3344、SB3346 和 SB3343 分别位于 0.5、0.7 和 0.9cM 处。我们通过对来自 23 个不同高粱品系的种子进行基因型和独脚金亚洲种和独脚金黑穗病菌发芽刺激素活性表型分析,验证了紧密连锁标记的有效性,这些品系大多已知具有抗独脚金特性。在 23 个测试品系中,21 个品系的标记与独脚金发芽刺激素活性共分离。lgs 位点同样影响了两种独脚金物种的发芽刺激素活性。鉴定出的标记将有助于利用标记辅助选择将该特性导入易感高粱品种。对高粱基因组序列的检查和与水稻基因组的比较分析表明,在精细定位区域(400kb)中可能存在一些影响独脚金内酯生物合成或分泌的候选基因。这项工作将为 lgs 基因的基于图谱的克隆奠定基础,并有助于阐明基于低独脚金发芽刺激素活性的抗性的确切机制。