Bradshaw John E, Hackett Christine A, Lowe Robert, McLean Karen, Stewart Helen E, Tierney Irene, Vilaro Marco D R, Bryan Glenn J
Scottish Crop Research Institute, Invergowrie, Dundee, DD2 5DA, UK.
Theor Appl Genet. 2006 Sep;113(5):943-51. doi: 10.1007/s00122-006-0353-8. Epub 2006 Jul 15.
Linkage analysis, Kruskal-Wallis analysis, interval mapping and graphical genotyping were performed on a potato diploid backcross family comprising 120 clones segregating for resistance to late blight. A hybrid between the Solanum tuberosum dihaploid clone PDH247 and the long-day-adapted S. phureja clone DB226(70) had been crossed to DB226(70) to produce the backcross family. Eighteen AFLP primer combinations provided 186 and 123 informative maternal and paternal markers respectively, with 63 markers in common to both parents. Eleven microsatellite (SSR) markers proved useful for identifying chromosomes. Linkage maps of both backcross parents were constructed. The results of a Kruskal-Wallis analysis, interval mapping and graphical genotyping were all consistent with a QTL or QTLs for blight resistance between two AFLP markers 30 cM apart on chromosome 4, which was identified by a microsatellite marker. The simplest explanation of the results is a single QTL with an allele from the dihaploid parent conferring resistance to race 1, 4 of P. infestans in the foliage in the glasshouse and to race 1, 2, 3, 4, 6, 7 in the foliage in the field and in tubers from glasshouse raised plants. The QTL was of large effect, and explained 78 and 51% of the variation in phenotypic scores for foliage blight in the glasshouse and field respectively, as well as 27% of the variation in tuber blight. Graphical genotyping and the differences in blight scores between the parental clones showed that all of the foliage blight resistance is accounted for by chromosome 4, whereas undetected QTLs for tuber resistance probably exist on other chromosomes. Graphical genotyping also explained the lack of precision in mapping the QTL(s) in terms of lack of appropriate recombinant chromosomes.
对一个由120个克隆组成的马铃薯二倍体回交群体进行了连锁分析、Kruskal-Wallis分析、区间作图和图形基因分型,这些克隆在晚疫病抗性方面存在分离。马铃薯双单倍体克隆PDH247与适应长日照的S. phureja克隆DB226(70)杂交,然后再与DB226(70)回交,从而产生了这个回交群体。18对AFLP引物组合分别提供了186个和123个母本和父本信息标记,其中63个标记为双亲共有。11个微卫星(SSR)标记被证明可用于鉴定染色体。构建了两个回交亲本的连锁图谱。Kruskal-Wallis分析、区间作图和图形基因分型的结果均表明,在4号染色体上两个相距30 cM的AFLP标记之间存在一个或多个晚疫病抗性QTL,该染色体由一个微卫星标记鉴定。对结果最简单的解释是存在一个单QTL,其二倍体亲本的等位基因赋予了对温室中叶片晚疫病致病疫霉1、4小种以及田间叶片和温室种植植株块茎中致病疫霉1、2、3、4、6、7小种的抗性。该QTL效应较大,分别解释了温室和田间叶片晚疫病表型评分变异的78%和51%,以及块茎晚疫病变异的27%。图形基因分型以及亲本克隆之间晚疫病评分的差异表明,所有叶片晚疫病抗性均由4号染色体决定,而未检测到的块茎抗性QTL可能存在于其他染色体上。图形基因分型还从缺乏合适的重组染色体方面解释了QTL定位缺乏精确性的原因。