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Resistance to powdery mildew in the pea cultivar Xucai 1 is conferred by the gene er1 被引量:3
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作者 Suli Sun Zhongyi Wang +3 位作者 Haining Fu Canxing Duan Xiaoming Wang Zhendong Zhu 《The Crop Journal》 SCIE CAS CSCD 2015年第6期489-499,共11页
Powdery mildew, caused by Erysiphe pisi D.C., is a major constraint to pea production worldwide. The pea cultivar Xucai 1 has shown high resistance to E. pisi under greenhouse and field conditions. The objectives of t... Powdery mildew, caused by Erysiphe pisi D.C., is a major constraint to pea production worldwide. The pea cultivar Xucai 1 has shown high resistance to E. pisi under greenhouse and field conditions. The objectives of this study were to identify and characterize genes conferring resistance to powdery mildew in Xucai 1. Three crosses, Qizhen 76 × Xucai 1,Bawan 6 × Xucai 1, and Xucai 1 × Bawan 6, were made to generate populations for genetic analysis. The resistance to E. pisi and segregation ratios in the F_1, F_2, and F_(2:3)populations suggested a single recessive gene conferring the resistance of Xucai 1. Bulked segregant analysis was used to map the resistance gene using two F2 populations. The resistance gene was close to markers AD60 and c5 DNAmet on linkage group VI with genetic distances of9.9 c M and 15.4 c M in the Xucai 1 × Bawan 6 F_2 population and 8.7 c M and 8.1 c M in the Qizhen 76 × Xucai 1 F_2 population, respectively, suggesting that the resistance gene was an er1 allele. This hypothesis was confirmed by comparison of the c DNA sequences of the Ps MLO1 gene between the parents and the Ps MLO1 wild type. Three distinct types of transcripts in Xucai 1, characterized by a 129-bp deletion and 155- and 220-bp insertions,were detected, consistent with the structure of the er1-2 allele. We concluded that resistance in Xucai 1 was conferred by er1-2 and that its linked markers will be useful in pea breeding programs. 展开更多
关键词 erYSIPHE pisi er1-2 PEA Powdery MILDEW Xucai1
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奥利亚罗非鱼雌激素β受体两种亚型cDNA的克隆、组织分布及雌激素对其表达的影响 被引量:4
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作者 兰滔 卢迈新 +4 位作者 杨丽萍 叶星 朱华平 高风英 黄樟翰 《水产学报》 CAS CSCD 北大核心 2010年第1期8-18,共11页
采用RT-PCR和RACE技术,克隆了奥利亚罗非鱼β雌激素受体基因(estrogen receptorβ,ERβ)两种亚型的cDNA全序列(ERβ1和ERβ2)。荧光定量PCR分析雌雄奥利亚罗非鱼两种亚型的组织分布,并观察注射外源雌激素对雄性奥利亚罗非鱼下丘脑-垂体... 采用RT-PCR和RACE技术,克隆了奥利亚罗非鱼β雌激素受体基因(estrogen receptorβ,ERβ)两种亚型的cDNA全序列(ERβ1和ERβ2)。荧光定量PCR分析雌雄奥利亚罗非鱼两种亚型的组织分布,并观察注射外源雌激素对雄性奥利亚罗非鱼下丘脑-垂体-性腺轴雌激素受体ERα和β(β1/β2)基因表达的影响。序列分析表明,ERβ1cDNA全长为4262bp,其中包含239bp5′非编码区,2349bp3′非编码区和1674bp的开放阅读框,共编码557个氨基酸。ERβ2 cDNA全长为2506bp,包含5′非编码区393bp,3′非编码区109bp,阅读框为2004bp,共编码667个氨基酸。氨基酸序列同源性分析显示奥利亚罗非鱼ERβ1与尼罗罗非鱼的相似性高达99.1%,而与鲈形目其它鱼类的相似性为82.6%~94.2%。ERβ2氨基酸序列与尼罗罗非鱼的相似性为98.7%,与大口黑鲈、虹鳟、底鳉及斑马鱼的相似性分别为81.8%、76.3%、64.7%和55.0%。在系统进化树上奥利亚罗非鱼的ERβ1和ERβ2分别与尼罗罗非鱼的相应受体聚类。奥利亚罗非鱼ERβ1/β2基因在所检测的10种组织中均有表达。ERβ1基因在卵巢、精巢、肝脏、肾脏和肠等组织的表达量均显著高于其他组织(P<0.05),以卵巢的表达量为最高。ERβ2基因在精巢、肝脏及肾脏组织的表达量较高(P<0.05)。ERβ1在卵巢、精巢、肠与下丘脑中的表达量显著高于ERβ2,其中卵巢中ERβ1的表达量是ERβ2的164倍。注射雌二醇(17beta-estradiol,E2)24h后雄性奥利亚罗非鱼下丘脑ERα/β1基因的表达上调,其中以ERα的升幅最大,且存在剂量依赖效应。在E2高剂量组(7.5mg/kg)下丘脑ERα的表达量显著升高(P<0.05),ERβ2基因的表达则没有显著变化。垂体中3个基因的表达在中低E2剂量(2.5mg/kg、5.0mg/kg)组均下调,而在E2高剂量(7.5mg/kg)组则上升,其中ERα的表达量显著升高(P<0.05)。精巢中ERβ2基因的表达量升高,以中、高剂量组(5.0、7.5mg/kg)的升幅最大(P<0.05),而ERα/β1两个基因的� 展开更多
关键词 奥利亚罗非鱼 β雌激素受体 erN和erβ2 组织分布 表达调控
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