Saha Malay C, Mian Rouf, Zwonitzer John C, Chekhovskiy Konstantin, Hopkins Andrew A
The Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK 73402, USA.
Theor Appl Genet. 2005 Jan;110(2):323-36. doi: 10.1007/s00122-004-1843-1. Epub 2004 Nov 19.
Tall fescue (Festuca arundinacea Schreb.) is commonly grown as forage and turf grass in the temperate regions of the world. Here, we report the first genetic map of tall fescue constructed with PCR-based markers. A combination of amplified fragment length polymorphisms (AFLPs) and expressed sequence tag-simple sequence repeats (EST-SSRs) of both tall fescue and those conserved in grass species was used for map construction. Genomic SSRs developed from Festuca x Lolium hybrids were also mapped. Two parental maps were initially constructed using a two-way pseudo-testcross mapping strategy. The female (HD28-56) map included 558 loci placed in 22 linkage groups (LGs) and covered 2,013 cM of the genome. In the male (R43-64) map, 579 loci were grouped in 22 LGs with a total map length of 1,722 cM. The marker density in the two maps varied from 3.61 cM (female parent) to 2.97 (male parent) cM per marker. These differences in map length indicated a reduced level of recombination in the male parent. Markers that revealed polymorphism within both parents and showed 3:1 segregation ratios were used as bridging loci to integrate the two parental maps as a bi-parental consensus. The integrated map covers 1,841 cM on 17 LGs, with an average of 54 loci per LG, and has an average marker density of 2.0 cM per marker. Homoeologous relationships among linkage groups of six of the seven predicted homeologous groups were identified. Three small groups from the HD28-56 map and four from the R43-64 map are yet to be integrated. Homoeologues of four of those groups were detected. Except for a few gaps, markers are well distributed throughout the genome. Clustering of those markers showing significant segregation distortion (23% of total) was observed in four of the LGs of the integrated map.
高羊茅(Festuca arundinacea Schreb.)是世界温带地区常见的饲料和草坪草。在此,我们报告了首张利用基于PCR的标记构建的高羊茅遗传图谱。高羊茅的扩增片段长度多态性(AFLP)和表达序列标签简单序列重复(EST-SSR)以及禾本科物种中保守的那些标记相结合用于图谱构建。从羊茅属×黑麦草属杂种中开发的基因组SSR也被定位。最初使用双向伪测交定位策略构建了两个亲本图谱。雌性(HD28-56)图谱包含558个位点,分布在22个连锁群(LG)中,覆盖基因组2013厘摩。在雄性(R43-64)图谱中,579个位点被归为22个LG,总图长为1722厘摩。两张图谱中的标记密度从每标记3.61厘摩(雌性亲本)到2.97厘摩(雄性亲本)不等。图谱长度的这些差异表明雄性亲本中的重组水平降低。在两个亲本中均显示多态性且呈现3:1分离比的标记被用作桥接位点,以将两个亲本图谱整合为一个双亲共识图谱。整合图谱在17个LG上覆盖1841厘摩,每个LG平均有54个位点,平均标记密度为每标记2.0厘摩。确定了七个预测的同源群中六个连锁群之间的同源关系。HD28-56图谱中的三个小群和R43-64图谱中的四个小群尚未整合。检测到其中四个群的同源物。除了少数间隙外,标记在整个基因组中分布良好。在整合图谱的四个LG中观察到那些显示显著分离畸变(占总数的23%)的标记的聚类。