Li Genqiao, Wang Ying, Chen Ming-Shun, Edae Erena, Poland Jesse, Akhunov Edward, Chao Shiaoman, Bai Guihua, Carver Brett F, Yan Liuling
Department of Plant and Soil Sciences, Oklahoma State University, 368 AG Hall, Stillwater, OK, 74078, USA.
Hard Winter Wheat Genetics Research Unit, USDA-ARS, Manhattan, KS, 66506, USA.
BMC Genomics. 2015 Feb 21;16(1):108. doi: 10.1186/s12864-015-1297-7.
One of the reasons hard red winter wheat cultivar 'Duster' (PI 644016) is widely grown in the southern Great Plains is that it confers a consistently high level of resistance to biotype GP of Hessian fly (Hf). However, little is known about the genetic mechanism underlying Hf resistance in Duster. This study aimed to unravel complex structures of the Hf region on chromosome 1AS in wheat by using genotyping-by-sequencing (GBS) markers and single nucleotide polymorphism (SNP) markers.
Doubled haploid (DH) lines generated from a cross between two winter wheat cultivars, 'Duster' and 'Billings' , were used to identify genes in Duster responsible for effective and consistent resistance to Hf. Segregation in reaction of the 282 DH lines to Hf biotype GP fit a one-gene model. The DH population was genotyped using 2,358 markers developed using the GBS approach. A major QTL, explaining 88% of the total phenotypic variation, was mapped to a chromosome region that spanned 178 cM and contained 205 GBS markers plus 1 SSR marker and 1 gene marker, with 0.86 cM per marker in genetic distance. The analyses of GBS marker sequences and further mapping of SSR and gene markers enabled location of the QTL-containing linkage group on the short arm of chromosome 1A. Comparative mapping of the common markers for the gene for QHf.osu-1A (d) in Duster and the Hf-resistance gene for QHf.osu-1A (74) in cultivar '2174' showed that the two Hf resistance genes are located on the same chromosome arm 1AS, only 11.2 cM apart in genetic distance. The gene at QHf.osu-1A (d) in Duster has been delimited within a 2.7 cM region.
Two distinct resistance genes exist on the short arm of chromosome 1A as found in the two hard red winter cultivars, 2174 and Duster. Whereas the Hf resistance gene in 2174 is likely allelic to one or more of the previously mapped resistance genes (H9, H10, H11, H16, or H17) in wheat, the gene in Duster is novel and confers a more consistent phenotype than 2174 in response to biotype GP infestation in controlled-environment assays.
硬红冬小麦品种“达斯特”(PI 644016)在大平原南部广泛种植的原因之一是它对黑森瘿蚊(Hf)的GP生物型具有持续高水平的抗性。然而,对于“达斯特”中Hf抗性的遗传机制知之甚少。本研究旨在通过使用简化基因组测序(GBS)标记和单核苷酸多态性(SNP)标记来解析小麦1AS染色体上Hf区域的复杂结构。
利用两个冬小麦品种“达斯特”和“比林斯”杂交产生的双单倍体(DH)系来鉴定“达斯特”中对Hf具有有效且一致抗性的基因。282个DH系对Hf生物型GP的反应分离符合单基因模型。使用GBS方法开发的2358个标记对DH群体进行基因分型。一个解释了88%总表型变异的主要QTL被定位到一个跨度为178 cM的染色体区域,该区域包含205个GBS标记、1个SSR标记和1个基因标记,遗传距离上每个标记为0.86 cM。对GBS标记序列的分析以及SSR和基因标记的进一步定位使得能够将包含QTL的连锁群定位到1A染色体的短臂上。对“达斯特”中QHf.osu - 1A(d)基因的共同标记与品种“2174”中QHf.osu - 1A(74)的Hf抗性基因进行比较定位,结果表明这两个Hf抗性基因位于同一染色体臂1AS上,遗传距离仅为11.2 cM。“达斯特”中QHf.osu - 1A(d)的基因已被限定在一个2.7 cM的区域内。
在两个硬红冬小麦品种“2174”和“达斯特”中,1A染色体短臂上存在两个不同的抗性基因。“2174”中的Hf抗性基因可能与小麦中先前定位的一个或多个抗性基因(H9、H10、H11、H16或H17)等位,而“达斯特”中的基因是新的,并且在控制环境试验中对GP生物型侵染的反应比“2174”表现出更一致的表型。