The Plant Protection Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, China.
Theor Appl Genet. 2011 May;122(7):1331-8. doi: 10.1007/s00122-011-1534-7. Epub 2011 Jan 28.
A new bacterial blight recessive resistance gene xa34(t) was identified from the descendant of somatic hybridization between an aus rice cultivar (cv.) BG1222 and susceptible cv. IR24 against Chinese race V (isolate 5226). The isolate was used to test the resistance or susceptibility of F(1) progenies and reciprocal crosses of the parents. The results showed that F(1) progenies appeared susceptibility there were 128R (resistant):378S (susceptible) and 119R:375S plants in F(2) populations derived from two crosses of BG1222/IR24 and IR24/BG1222, respectively, which both calculates into a 1R:3S ratio. 320 pairs of stochastically selected SSR primers were used for genes' initial mapping. The screened results showed that two SSR markers, RM493 and RM446, found on rice chromosome 1 linked to xa34(t). Linkage analysis showed that these two markers were on both sides of xa34(t) with the genetic distances 4.29 and 3.05 cM, respectively. The other 50 SSR markers in this region were used for genes' fine mapping. The further results indicated that xa34(t) was mapped to a 1.42 cM genetic region between RM10927 and RM10591. In order to further narrow down the genomic region of xa34(t), 43 of insertion/deletion (Indel) markers (BGID1-43) were designed according to the sequences comparison between japonica and indica rice. Parents' polymorphic detection and linkage assay showed that the Indel marker BGID25 came closer to the target gene with a 0.4 cM genetic distance. A contig map corresponding to the locus was constructed based on the reference sequences aligned by the xa34(t) linked markers. Consequently, the locus of xa34(t) was defined to a 204 kb interval flanked by markers RM10929 and BGID25.
从 aus 水稻品种 (cv.) BG1222 和敏感品种 cv.IR24 体细胞杂交的后代中,鉴定出一个新的细菌性枯萎病隐性抗性基因 xa34(t),该品种对中国品种 V (分离株 5226) 具有抗性。使用该分离株测试 F1 后代和双亲的正反交的抗性或敏感性。结果表明,F1 后代出现敏感性,BG1222/IR24 和 IR24/BG1222 的两个杂交 F2 群体中分别有 128R(抗性):378S(敏感性)和 119R:375S 植株,两者均计算为 1R:3S 比值。用 320 对随机选择的 SSR 引物进行基因的初步作图。筛选结果表明,在水稻染色体 1 上发现了与 xa34(t) 连锁的两个 SSR 标记 RM493 和 RM446。连锁分析表明,这两个标记位于 xa34(t) 的两侧,遗传距离分别为 4.29 和 3.05 cM。该区域的其他 50 个 SSR 标记用于基因的精细作图。进一步的结果表明,xa34(t) 被定位在 RM10927 和 RM10591 之间的 1.42 cM 遗传区域。为了进一步缩小 xa34(t) 的基因组区域,根据粳稻和籼稻序列比较设计了 43 个插入/缺失 (Indel) 标记 (BGID1-43)。亲本的多态性检测和连锁分析表明,Indel 标记 BGID25 与目标基因的遗传距离更近,为 0.4 cM。根据与 xa34(t) 连锁标记对齐的参考序列构建了对应于该位点的连续图谱。因此,将 xa34(t) 的位点定义为 RM10929 和 BGID25 标记之间 204 kb 的区间。