Matsui K, Kiryu Y, Komatsuda T, Kurauchi N, Ohtani T, Tetsuka T
National Agricultural Research Center for Kyushu Okinawa Region, Nishigoshi, Kumamoto, Japan.
Genome. 2004 Jun;47(3):469-74. doi: 10.1139/g04-007.
Shattering habit in buckwheat has two forms: brittle pedicel and weak pedicel. Brittle pedicel is observed in wild buckwheat, but not in cultivated buckwheat. Brittle pedicel in buckwheat is produced by two complementary, dominant genes, Sht1 and Sht2. The sht1 locus is linked to the S locus; almost all common buckwheat cultivars possess the allele sht1. To detect molecular makers linked to the sht1 locus, we used amplified fragment-length polymorphism (AFLP) analysis in combination with bulked segregant analysis of segregating progeny of a cross between a non-brittle common buckwheat and a brittle self-compatible buckwheat line. We screened 312 primer combinations and constructed a linkage map around the sht1 locus by using 102 F2 plants. Five AFLP markers were linked to the sht1 locus. Two of these, e54m58/610 and e55m46/320, cosegregated with the sht1 locus without recombination. The two AFLP markers were converted to STS markers according to the sequence of the AFLPs. The STS markers are useful for marker-assisted selection of non-brittle pedicel plants and provides a stepping-stone for map-based cloning and characterization of the gene encoding non-brittle pedicel.
脆花梗和弱花梗。脆花梗在野生荞麦中可见,但在栽培荞麦中未见。荞麦中的脆花梗由两个互补的显性基因Sht1和Sht2产生。sht1位点与S位点连锁;几乎所有普通荞麦品种都具有等位基因sht1。为了检测与sht1位点连锁的分子标记,我们将扩增片段长度多态性(AFLP)分析与非脆粒普通荞麦和脆粒自交亲和荞麦品系杂交后代的分离群体分组分析法相结合。我们筛选了312对引物组合,并利用102株F2植株构建了围绕sht1位点的连锁图谱。五个AFLP标记与sht1位点连锁。其中两个,e54m58/610和e55m46/320,与sht1位点共分离且无重组。根据AFLP的序列将这两个AFLP标记转化为STS标记。这些STS标记可用于非脆花梗植株的标记辅助选择,并为基于图谱的克隆和编码非脆花梗基因的表征提供了一个跳板。