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Characterization and mapping of a white panicle mutant gene in rice 被引量:6
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作者 lihongchang QIANQian +3 位作者 WANGYun LIXiaobo ZHULihuang XUJichen 《Chinese Science Bulletin》 SCIE EI CAS 2003年第5期457-459,共3页
A spontaneous white panicle mutant was found from the F6 progenies of an indica/japonica cross. The mu-tant exhibits white stripes on its basal leaves while the pani-cles, rachis and pedicel are milky white colored at... A spontaneous white panicle mutant was found from the F6 progenies of an indica/japonica cross. The mu-tant exhibits white stripes on its basal leaves while the pani-cles, rachis and pedicel are milky white colored at flowering stage. Genetic analysis in an F2 population from the cross of Zhi7/white panicle mutant indicates that the white panicle phenotype is controlled by a single recessive nuclear gene, tentatively termed as wp(t). Using microsatellite markers, the wp(t) gene was anchored between the markers of SSR101 and SSR63.9 with a map distance of 2.3 and 0.8 cM, respec-tively, and co-segregated with the marker of SSR17 on rice chromosome 1. 展开更多
关键词 水稻 蛋白 圆锥花序 突变基因 基因作图 基因表达
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Genetic analysis and fine mapping of a lax mutant in rice 被引量:1
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作者 WANGYun XIAOHan +3 位作者 QIANQian lihongchang LIShigui ZHULihuang 《Chinese Science Bulletin》 SCIE EI CAS 2003年第19期2072-2076,共5页
We have analyzed a lax mutant that exhibits altered panicle architecture in rice. The primary and secondary rachis-branches are normally initiated and each branch ends in a terminal spikelet, but all the lateral spike... We have analyzed a lax mutant that exhibits altered panicle architecture in rice. The primary and secondary rachis-branches are normally initiated and each branch ends in a terminal spikelet, but all the lateral spikelets are absent and the terminal spikelet displays variegated structures in the mutant. An F2 population from the cross between the lax mutant and a japonica variety, W11, was constructed and analyzed. Using microsatellite and CAPS markers, the lax locus was mapped on the long arm of chromosome 1, co-segregated with a CAPS marker, LZ1, within an interval of 0.28 cM between a CAPS marker, HB2, and a microsatellite marker, MRG4389. RT-PCR analysis revealed that the expressions of the rice B-function MADS-box genes OsMADS2, OsMADS4, OsMADS16 and OsMADS3 were significantly reduced, whereas the expression of the rice A-function gene RAP1A was not altered. 展开更多
关键词 基因分析 水稻 突变异种 微量标记 CAPS 基因定位
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