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将来自 Oryza australiensis 的褐飞虱抗性和早熟基因进行分子标记,并导入栽培稻 O. sativa。

Molecular tagging of genes for brown planthopper resistance and earliness introgressed from Oryza australiensis into cultivated rice, O. sativa.

出版信息

Genome. 1994 Apr;37(2):217-21. doi: 10.1139/g94-030.

Abstract

Restriction fragment length polymorphism analysis was carried out to tag the alien genes for brown planthopper (BPH) resistance and earliness introgressed from wild species Oryza australiensis into cultivated rice, O. sativa L. One introgression line (IR65482-4-136-2-2), resistant to biotypes 1, 2, and 3 of BPH and early in flowering, was selected from BC2F4 of the cross between O. sativa (IR31917-45-3-2) and O. australiensis (accession 100882). Recurrent parent, O. australiensis, and introgression line were surveyed for RFLP using probes of chromosomes 10 and 12. Two probes, RG457 and CDO98, detected introgression from O. australiensis. Cosegregation between introgressed characters and molecular markers was studied in F2 derived from the cross between the introgression line and recurrent parent. The gene for BPH resistance is linked with RG457 of chromosome 12 at a distance of 3.68 +/- 1.29 cM, and the gene for earliness is linked with CDO98 of chromosome 10 at a distance of 9.96 +/- 3.28 cM. Such close linkage is useful in marker-based selection while transferring BPH resistance from introgression line into other elite breeding lines. Introgression at the molecular level indicates that the mechanism of alien gene transfer is probably genetic recombination through crossing over rather than substitution of whole or large segment of chromosomes of wild species.

摘要

采用限制性片段长度多态性(RFLP)分析,将从野生种 Oryza australiensis 导入栽培稻 O. sativa 的褐飞虱(BPH)抗性和早熟基因进行标记。从 O. sativa(IR31917-45-3-2)与 O. australiensis(100882 号)杂交的 BC2F4 中选择了一个对 BPH 生物型 1、2 和 3 具有抗性且开花早的导入系(IR65482-4-136-2-2)。用染色体 10 和 12 的探针对轮回亲本 O. australiensis 和导入系进行 RFLP 调查。两个探针 RG457 和 CDO98 检测到来自 O. australiensis 的导入。在导入系与轮回亲本杂交的 F2 中,研究了导入性状与分子标记的共分离。BPH 抗性基因与染色体 12 上的 RG457 连锁,距离为 3.68 +/- 1.29 cM,早熟基因与染色体 10 上的 CDO98 连锁,距离为 9.96 +/- 3.28 cM。这种紧密连锁在将 BPH 抗性从导入系转移到其他优良育成系时,可用于基于标记的选择。分子水平的导入表明,外源基因转移的机制可能是通过交叉重组而不是野生种的整条或大片段染色体的替代进行的遗传重组。

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