作物学报 ›› 2009, Vol. 35 ›› Issue (5): 861-866.doi: 10.3724/SP.J.1006.2009.00861
李艳秋1,苏志芳1,2,**,王立新1,季伟1,姚骥3,赵昌平1,*
LI Yan-Qiu1,SU Zhi-Fang12**,WANG Li-Xin1,JI Wei1,YAO Ji3,ZHAO Chang-Ping1*
摘要:
高密度的分子标记遗传图谱是QTL定位、图位克隆和分子标记辅助选择等研究的基础。以小麦品种“京花1号/小白冬麦”的双单倍体(DH)群体和“农大015/复壮30”的重组自交系(RIL)群体为作图群体,选用在DH群体双亲间的339个多态性标记和在RIL群体双亲间的343个多态性标记分析作图群体各个株系的基因型,对本中心近年开发的SCAR、EST-SSR标记以及他人开发的SSR、EST-SSR标记进行了染色体定位,并利用连锁分析软件Joinmap 4.0将2个作图群体的结果整合,最终构建了10个连锁群,将217个SSR、EST-SSR和SCAR位点定位在9条染色体上,进一步提高了小麦遗传图谱的密度。
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