[Objective]The aim was to study the effective factors on culturing Prunus salicina cv.Zaoshi embryos in vitro.[Method]Different age,culture medium and GA3 which affected culturing of prumssalicina embryos were discuss...[Objective]The aim was to study the effective factors on culturing Prunus salicina cv.Zaoshi embryos in vitro.[Method]Different age,culture medium and GA3 which affected culturing of prumssalicina embryos were discussed.[Result]The result showed that on the part of 26-41 d,after the blooming period,the embryos remained tiny and retained endosperms and showed no signs of change after having cultured for three generations.On the part of 48 d,after the blooming period,the endosperms had disappeared,the embryos kept growing until they filled the seed cavity;when they were planted on the MS culture medium,their survival rate reached 77%,in its first generation,the response of embryos was discernible.On the part of 65 d,after the blooming period,4.5% of their embryos grew into shoots on the MS culture medium;with the age of embryos growing,the survival rate of shoots increased until it reached 26% when the fruits went into ripeness;the embryos produced calli in their first generation of culturing.On the part of 65-83 d,after the blooming period,the embryos produced calli through more than 2-3 generations.On the part of 88 d,after the blooming period,the survival rate of shoots on the WPM culturing base doubled compared with that on the MS culturing base;on the same culture medium,the embryos were inhibited from growing into shoots when BA,KT or 2,4-D was added on to the culture medium.The survival rate of shoots was increased remarkably when the seeds were treated in 1 000 mg/L GA3.[Conclusion] This study provided experimental basis for the establishment of Prunus salicina cv.Zaoshi,embryos rescue techniques and cross breading.展开更多
[ Objective] This study aimed to investigate the genetic variation between hybrids and their parents, and to find a rapid identification method. [ Method ] The progenies between Prunus armeniaca （ apricot ） Katy and...[ Objective] This study aimed to investigate the genetic variation between hybrids and their parents, and to find a rapid identification method. [ Method ] The progenies between Prunus armeniaca （ apricot ） Katy and Prunus salicina （plum） Moriteni were analyzed by means of RAPD and SSR molecular markers. [ Result] We found the differences in the electrophoresis bands between progenies and their parents, indicating that hybrid seedlings obtained in this study were real. [ Conclusion ] The combination of the above methods is effective and fast to identify the hybrids, and can shorten the breeding period.展开更多
Embryo abortion stage and rescue system of hybrids were studied in the distant hybridizationbetween plum and apricot. Identification of the hybrids was also made. The resultsshowed: (1) Embryo abortion started from th...Embryo abortion stage and rescue system of hybrids were studied in the distant hybridizationbetween plum and apricot. Identification of the hybrids was also made. The resultsshowed: (1) Embryo abortion started from three weeks after pollination. (2) The germinationand growth of embryos were different at different growth stages, which could germinateand grow with PF value>0.5, but failed with PF value<0.5. In embryo rescue system ofhybrids, the best germination and differentiation medium was MS+6-BA 2mgL-1+IAA 0.3mgL-1,the rate of germination and differentiation reached up to 80%, bud induction andmultiplication medium was MS+6-BA 1.5mgL-1+IAA 0.3mgL-1, rooting medium was 1/2 MS+IAA0.8mgL-1. Some hybrids were transplanted into the field successfully. (3) Leaf shapeinvestigation and identification by S allele-specific PCR and RAPDs showed that thehybrids were true ones.展开更多
为开发槜李EST-SSR标记,本研究利用MISA软件筛选了槜李花转录组测序获得的35584条Unigenes,对其SSR信息进行分析后,利用Primer Premier 3.0软件设计EST-SSR引物,并随机选取40对SSR引物对12个李品种进行EST-SSR引物筛选及多态性分析。结...为开发槜李EST-SSR标记,本研究利用MISA软件筛选了槜李花转录组测序获得的35584条Unigenes,对其SSR信息进行分析后,利用Primer Premier 3.0软件设计EST-SSR引物,并随机选取40对SSR引物对12个李品种进行EST-SSR引物筛选及多态性分析。结果发现,在槜李花转录组中共搜索到个10791个SSR位点,分布于8433条Unigenes,SSR发生频率为23.70%,平均每3.71 kb含有1个SSR;SSR重复基元中二核苷酸重复出现频率最高,占总SSR数量的52.98%,其次为三核苷酸重复(占24.00%)和单核苷酸重复(占20.95%);二核苷酸重复基元以AG/CT为主(85.95%),三核苷酸重复基元以AAG/CTT为主(31.24%)。利用Primer Premier 3.0软件共设计出9870对候选引物,随机选择40对引物对12个李品种进行SSR引物筛选及多态性分析。40对引物均能扩增出预期大小的条带,有效扩增效率为100%,40对引物中有5对引物在12个李品种中表现出多态性。本研究开发的EST-SSR标记可为李属植物遗传多样性分析提供丰富的候选标记,同时可为槜李发育相关功能基因定位、遗传图谱构建、及分子标记辅助育种等研究提供帮助。展开更多
基金Support by Major Science and Technology Projects of Guangdong Province (2004A20102002)~~
文摘[Objective]The aim was to study the effective factors on culturing Prunus salicina cv.Zaoshi embryos in vitro.[Method]Different age,culture medium and GA3 which affected culturing of prumssalicina embryos were discussed.[Result]The result showed that on the part of 26-41 d,after the blooming period,the embryos remained tiny and retained endosperms and showed no signs of change after having cultured for three generations.On the part of 48 d,after the blooming period,the endosperms had disappeared,the embryos kept growing until they filled the seed cavity;when they were planted on the MS culture medium,their survival rate reached 77%,in its first generation,the response of embryos was discernible.On the part of 65 d,after the blooming period,4.5% of their embryos grew into shoots on the MS culture medium;with the age of embryos growing,the survival rate of shoots increased until it reached 26% when the fruits went into ripeness;the embryos produced calli in their first generation of culturing.On the part of 65-83 d,after the blooming period,the embryos produced calli through more than 2-3 generations.On the part of 88 d,after the blooming period,the survival rate of shoots on the WPM culturing base doubled compared with that on the MS culturing base;on the same culture medium,the embryos were inhibited from growing into shoots when BA,KT or 2,4-D was added on to the culture medium.The survival rate of shoots was increased remarkably when the seeds were treated in 1 000 mg/L GA3.[Conclusion] This study provided experimental basis for the establishment of Prunus salicina cv.Zaoshi,embryos rescue techniques and cross breading.
基金Supported by the Natural Science Foundation of Shandong Province(Q2008D01)Program for Science Research Development of Higher Education Institutions of Shandong Province(J09LC54)
文摘[ Objective] This study aimed to investigate the genetic variation between hybrids and their parents, and to find a rapid identification method. [ Method ] The progenies between Prunus armeniaca （ apricot ） Katy and Prunus salicina （plum） Moriteni were analyzed by means of RAPD and SSR molecular markers. [ Result] We found the differences in the electrophoresis bands between progenies and their parents, indicating that hybrid seedlings obtained in this study were real. [ Conclusion ] The combination of the above methods is effective and fast to identify the hybrids, and can shorten the breeding period.
基金supported by the Technological Production Transformation Foundation by the Ministry of Science and Technology of China(2002370010495)the foundation of Shandong Fruit Tree Three-Zero Project
文摘Embryo abortion stage and rescue system of hybrids were studied in the distant hybridizationbetween plum and apricot. Identification of the hybrids was also made. The resultsshowed: (1) Embryo abortion started from three weeks after pollination. (2) The germinationand growth of embryos were different at different growth stages, which could germinateand grow with PF value>0.5, but failed with PF value<0.5. In embryo rescue system ofhybrids, the best germination and differentiation medium was MS+6-BA 2mgL-1+IAA 0.3mgL-1,the rate of germination and differentiation reached up to 80%, bud induction andmultiplication medium was MS+6-BA 1.5mgL-1+IAA 0.3mgL-1, rooting medium was 1/2 MS+IAA0.8mgL-1. Some hybrids were transplanted into the field successfully. (3) Leaf shapeinvestigation and identification by S allele-specific PCR and RAPDs showed that thehybrids were true ones.
文摘为开发槜李EST-SSR标记,本研究利用MISA软件筛选了槜李花转录组测序获得的35584条Unigenes,对其SSR信息进行分析后,利用Primer Premier 3.0软件设计EST-SSR引物,并随机选取40对SSR引物对12个李品种进行EST-SSR引物筛选及多态性分析。结果发现,在槜李花转录组中共搜索到个10791个SSR位点,分布于8433条Unigenes,SSR发生频率为23.70%,平均每3.71 kb含有1个SSR;SSR重复基元中二核苷酸重复出现频率最高,占总SSR数量的52.98%,其次为三核苷酸重复(占24.00%)和单核苷酸重复(占20.95%);二核苷酸重复基元以AG/CT为主(85.95%),三核苷酸重复基元以AAG/CTT为主(31.24%)。利用Primer Premier 3.0软件共设计出9870对候选引物,随机选择40对引物对12个李品种进行SSR引物筛选及多态性分析。40对引物均能扩增出预期大小的条带,有效扩增效率为100%,40对引物中有5对引物在12个李品种中表现出多态性。本研究开发的EST-SSR标记可为李属植物遗传多样性分析提供丰富的候选标记,同时可为槜李发育相关功能基因定位、遗传图谱构建、及分子标记辅助育种等研究提供帮助。
