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Validation of molecular markers for covered smut resistance and marker-assisted introgression of loose and covered smut resistance into hulless barley

机译:验证分子标记对黑穗病的抗性和标记辅助将无性和被覆盖的黑穗病渗入大麦中

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Inheritance of covered smut resistance was investigated in three hulless x hulled barley populations (CDC Candle/Q21861, CDC McGwire/Q21861, and CDC McGwire/TR640). Greenhouse and/or field screening indicated resistance was controlled by a single major gene from Q21861 and TR640. Three molecular markers (UhR 450, aHor 2 and OPO6) linked to the covered smut resistance gene (Ruhq) in the hulled line Q21861 were assessed for their usefulness in selecting resistant hulless barley. All markers were linked to covered smut resistance in the three populations evaluated, although aHor 2 was only polymorphic in CDC Candle/Q21861. Two strategies, doubled haploidy (DH) and marker-assisted backcrossing (MAB), were used to simultaneously introgress Ruhq and loose smut resistance (Run8) into the hulless barley cultivar CDC McGwire. Thirty-five DH lines were developed from a cross of hulless loose smut resistant line SH00752 (CDC McGwire/TR251) by hulless covered smut resistant line SH01470 (CDC McGwire/Q21861). By screening the 35 DH lines for each of the markers, 14 were identified as positive for both. Following three rounds of screening by artificial inoculation, 12 of those were identified as resistant to both diseases. In the MAB program, blind selection based solely on markers was conducted through the BCF generation; lines resistant to both diseases were obtained. One line, designated HB390, is being advanced to 2nd year of the Western Canadian Hulless Barley Co-operative yield trials, the final step to release of a cultivar for commercial production in Canada. These results confirm that molecular markers can be used in either DH or MAB programs to assist in the rapid introgression of simply inherited disease resistance genes into elite lines, with considerable time and cost savings.
机译:在三个无壳x有壳大麦种群(CDC Candle / Q21861,CDC McGwire / Q21861和CDC McGwire / TR640)中研究了覆盖的黑穗病抗性的遗传。温室和/或田间筛选表明抗性由来自Q21861和TR640的单个主要基因控制。评估了与去壳线Q21861中覆盖的黑穗病抗性基因(Ruhq)相关的三个分子标记(UhR 450,aHor 2和OPO6)在选择抗性无性大麦中的有用性。尽管aHor 2在CDC Candle / Q21861中仅是多态性的,但在所评估的三个种群中,所有标记均与覆盖的黑穗病抗性相关。双重单倍体(DH)和标记辅助回交(MAB)两种策略被用于同时将Ruhq和宽松的黑穗病抗性(Run8)引入到无h的大麦品种CDC McGwire中。从无害的抗黑丝抗性线SH00752(CDC McGwire / TR251)的杂交中,开发了三十五个DH线。通过针对每种标记物筛选35条DH谱线,鉴定出14条对两种标记均为阳性。经过三轮人工接种筛选后,其中的12种被鉴定为对两种疾病均具有抗药性。在MAB程序中,通过BCF生成仅基于标记的盲选。获得了对两种疾病都有抗性的品系。一条命名为HB390的品系正在进入加拿大西部无麦大麦合作社产量试验的第二年,这是在加拿大商业化生产品种的最后一步。这些结果证实了分子标记可用于DH或MAB程序,以帮助将简单遗传的抗病基因快速渗入优良品系,从而节省大量时间和成本。

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