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首页> 外文期刊>Molecular biology reports >Genetic analysis and fine mapping of a rice brown planthopper (Nilaparvata lugens Stal) resistance gene bph19(t)
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Genetic analysis and fine mapping of a rice brown planthopper (Nilaparvata lugens Stal) resistance gene bph19(t)

机译:水稻褐飞虱抗性基因bph19(t)的遗传分析和精细定位

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Genetic analysis and fine mapping of a resistance gene against brown planthopper (BPH) biotype 2 in rice was performed using two F-2 populations derived from two crosses between a resistant indica cultivar (cv.), AS20-1, and two susceptible japonica cvs., Aichi Asahi and Lijiangxintuanheigu. Insect resistance was evaluated using F-1 plants and the two F-2 populations. The results showed that a single recessive gene, tentatively designated as bph19(t), conditioned the resistance in AS20-1. A linkage analysis, mainly employing microsatellite markers, was carried out in the two F-2 populations through bulked segregant analysis and recessive class analysis (RCA), in combination with bioinformatics analysis (BIA). The resistance gene locus bph19(t) was finely mapped to a region of about 1.0 cM on the short arm of chromosome 3, flanked by markers RM6308 and RM3134, where one known marker RM1022, and four new markers, b1, b2, b3 and b4, developed in the present study were co-segregating with the locus. To physically map this locus, the bph19(t)-linked markers were landed on bacterial artificial chromosome or P1 artificial chromosome clones of the reference cv., Nipponbare, released by the International Rice Genome Sequencing Project. Sequence information of these clones was used to construct a physical map of the bph19(t) locus, in silico, by BIA. The bph19(t) locus was physically defined to an interval of about 60 kb. The detailed genetic and physical maps of the bph19(t) locus will facilitate marker-assisted gene pyramiding and cloning.
机译:水稻的抗褐飞虱(BPH)生物型2抗性基因的遗传分析和精细定位是使用两个F-2群体进行的,该群体来自两个抗性in稻品种(cv。),AS20-1和两个易感粳稻之间的杂交,朝日爱知和丽江新世界黑姑。使用F-1植物和两个F-2种群评估了抗虫性。结果表明,单个隐性基因暂定为bph19(t)调节了AS20-1的抗性。通过大量的分离子分析和隐性分类分析(RCA)结合生物信息学分析(BIA),在两个F-2种群中进行了主要使用微卫星标记的连锁分析。将抗性基因座bph19(t)精细定位到3号染色体短臂上约1.0 cM的区域,侧翼是标记RM6308和RM3134,其中一个已知标记RM1022,以及四个新标记b1,b2,b3和在本研究中开发的b4与基因座共分离。为了对这个基因座进行物理定位,将bph19(t)连锁标记置于国际稻米基因组测序项目发布的参考品种Nipponbare的细菌人工染色体或P1人工染色体克隆上。这些克隆的序列信息用于通过BIA在计算机上构建b​​ph19(t)基因座的物理图谱。 bph19(t)基因座在物理上被定义为大约60 kb的间隔。 bph19(t)基因座的详细遗传和物理图谱将有助于标记辅助的基因金字塔和克隆。

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