水稻雄性不育突变体ms102的鉴定和基因定位
王霞1, 严维1, 周志勤2, 常振仪1, 郑敏婷1, 唐晓艳1,2, 吴建新1,*(
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Identification and Mapping of a Rice Male Sterility Mutant ms102
Xia Wang1, Wei Yan1, Zhiqin Zhou2, Zhenyi Chang1, Minting Zheng1, Xiaoyan Tang1,2, Jianxin Wu1,*()
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图5. 花药发育相关基因在野生型和ms102花药中的表达
通过qRT-PCR检测野生型与ms102突变体中花药发育7-12时期相关基因的表达量。以OsACTIN1作为内参, 数据为平均值±标准差(n=3)。* P<0.05, ** P<0.01, *** P<0.001
Figure 5. Expression of genes related to pollen development in WT and ms102 anthers
Anthers at stages 7-12 were used for qRT-PCR. OsACTIN1 served as an internal control. Data are shown as means±SD (n=3). * P<0.05, ** P<0.01, *** P<0.001
