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Oryza glumaepatula Steud. introgression lines in rice: identification of genes for reproductive barriers

机译:oryza glumaepatula steud。大米的血栓增速:鉴定生殖障碍基因

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To broaden rice genetic resources, we developed introgression lines carrying Oryza glumaepatufa (IRGC-Acc. 105668} and O. sativa cv, Taichung 65 cytoplasm. These lines contain overlapped O. glumaepatula chromosomal segments that covered most parts ofthe O. glumaepatula genome in the Taichung 65 genetic background, Introgression lines were developed through repeated backcrossing with Taichung 65 as a recurrent parent, Candidate lines were selected using 106 restriction fragment length polymorphism (RFLP) markers well distributed on 12 rice chromosomes. During the process of development, two reproductive barriers, hybrid weakness and pollen semisterility, were observed in the backcross populations. Hybrid weakness was attributed to the interaction between O. glumaepatula cytoplasm and the nuclear genome of Taichung 65. The dominant allele of O. glumaepatula restored the hybrid weakness of the plants having O. glumaepatula cytoplasm. The gene responsible for hybrid weakness restoration was designatedRhw (hybrid weakness restoration for O. glumaepatula cytoplasm) and was closely linked to RFLP marker C1115 on chromosome 8. Two F_1 pollen semisterility genes, S22(t) and S23(t), were closely linked to RFLP markers S910 on chromosome 2 and C1340 on chromosome 7, respectively. Since the O. glumaepatula homozygous alleles were not observed at the S910 locus in the BC_4F_2 population, it seemed that the pollen having the O. glumaepatula allele at the S22(t) locus aborted.
机译:为了扩大水稻遗传资源,我们开发了携带oryza glumaepatufa(IRGC-ACC。105668}和O. Sativa CV,Taicheng 65细胞质的血液突出线。这些线含有重叠的O. glumaepatula染色体段,这些系列覆盖了O. glumaepatula基因组的大多数部分Taichung 65遗传背景,通过用Taichung 65重复回复,作为复发父母,使用106个限制性片段长度多态性(RFLP)标记分布在12米染色体上,选择候选线。在开发过程中,两个生殖障碍在回复群体中观察到杂交弱点和花粉清晰度。杂交弱点归因于O. glumapatula细胞质与Taicheng 65的核基因组之间的相互作用。O. glumaepatula的显性等位基因恢复了o的植物的混合弱点。Glumaepatula细胞质。负责混合弱恢复的基因S指定rhw(o. glumapatula细胞质的混合弱恢复),并与染色体8的RFLP标记C1115密切相关。两个F_1花粉混合发生基因,S22(t)和S23(t)与染色体2的RFLP标记S910密切相关和C1340分别在染色体7上。由于在BC_4F_2群中的S910基因座上未观察到甘蓝夸普拉纯合的等位基因,因此似乎在S22(T)基因座中具有O. glumaepatula等位基因的花粉。

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