共查询到20条相似文献,搜索用时 156 毫秒
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对9份杂稻新质源不育系及3份核供体相同的滇一型不育系水稻的花粉败育特点和花时特征进行了研究。结果表明:绝大部分新质源不育系与滇一型不育系具有相同的花粉败育特点,以染败为主,而IR58025/南29-48//测64为细胞质源的楚粳23A,花粉败育以典败为主,云恢290//旱谷香糯/滇榆为细胞质源的合系42A,圆败、典败花粉占总花粉量的一半,以IR58025/南29-48//测64为细胞质源的合系42A,圆败、典败花粉占总花粉量的20%。新质源不育系与滇一型不育系花时相比,各具特色,表现不一,以核供体楚粳23的花时集中,花时高峰出现;以核供体为合系42的花时集中且提前现象,有利于制种;以核供体为合系41花时不集中,但开花较晚。 相似文献
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普通小麦T型,V型和K型细胞质雄性不育系花粉败育机理的细胞学研究 总被引:11,自引:2,他引:11
从细胞学的角度对小麦83(21)35核背景的T型、V型和K型细胞质雄性不育系的花粉败育机理进行了研究。发现三类不育系的小孢子发生过程基本正常,T型不育系的花粉主要在小孢子后期发生败育,以典败型和圆败型为主;V型不育系的花粉主要在小孢子后期至二细胞花粉期败育,以圆败型和浅染败型为主;而K型不育系的花粉主要在二细胞花粉后期至三细胞花粉期败育,以浅染败型和深染败型为主。药室合并现象普遍发生是T型不育系花药的一个突出特点,而V型和K型人育系花药各壁层的发育是正常的。核质发育关系不协调是不育系花粉败育的根本原因。细胞学观察结果可以作为不育细胞质类型划分的一项参考指标。 相似文献
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水稻不同细胞质类型雄性不育系的研究 总被引:34,自引:0,他引:34
收集了我国22个不同细胞质来源的水稻雄性不育系,并进行花粉育性观察。22个不育系的花粉败育,可以分为三个类型:“典败”型(不规则败育型);“圆败”型和“染败”型。对各类典型不育系和保持系的特征特性观察表明:异源核质结合引起一系列生理代谢异常;除雄性不育外,还导致植株变矮、卡颈、穗颈变短、第一节间变短、每穗粒数减 相似文献
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水稻质核互作孢子体雄性不育性的基因分析 总被引:22,自引:3,他引:19
把花粉育性划分为可育、染败、圆败和典败四种类型,对三种不同细胞质来源的四个水稻雄性不育系的质核互作雄性不育性进行基因分析。结果表明,野败珍汕97A、野败二九矮4A、冈比亚卡二九矮7A 和毛早壳八四早8A 的质核互作雄性不育性均由两对隐性育性恢复基因 rf_1 rf_1 rf_2 rf_2控制,属孢子体不育类型。IR24具有相应的两对显性 相似文献
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乙烯与水稻细胞质雄性不育的关系 总被引:11,自引:1,他引:10
从幼穗发育的IV到VII期,水稻细胞质雄性不育系(珍汕97A)幼穗和叶片的ACC含量和乙烯释放速率均高于其保持系(珍汕97B)。外施乙烯释放剂乙烯利使保持系花粉可育度明显下降;外施ACC合成酶抑制剂AVG引起两系幼穗ACC含量和乙烯释放速率下降,并使不育系花粉育性得以部分恢复,而在外施AVG的同时再施以乙烯利则AVG的恢复作用消失。 相似文献
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线粒体DNA由来的RAPD标记能鉴别水稻雄性不育和可育细胞质 总被引:9,自引:0,他引:9
以野败型细胞质的水稻雄性不育系珍汕97A及其保持系珍汕97B的总DNA为模板,从100个引物中筛选到OPA12对珍汕97A能扩增出一条1600 bp的特异带.用OPA12扩增野败型细胞质的龙特浦A及其保持系龙特浦B、矮败型细胞质的协青早A及其保持系协青早B、恢复系明恢63、珍汕97A/明恢63的F1和F2个体的总DNA,不育系、F1和F2所有调查个体都有16 相似文献
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Isolation and genetic characterization of a fertility-restoring revertant induced from cytoplasmic male sterile rice 总被引:2,自引:0,他引:2
Summary A male fertile revertant was isolated from M1 of a cytoplasmic male sterile indica rice line II-32A, the dry seeds of which were treated with 60Co- rays at a dose of 290 Gy. The acquired revertant T24 was morphologically and agronomically similar to II-32B, the maintainer of II-32A. Testcrosses of the revertant with II-32A and Zhenshan 97A showed that the revertant was able to restore the fertility of CMS lines. Genetic analysis of the progenies between T24 and II-32A, Zhenshan 97A XieqingzaoA and DZhenshan 97A, which have different cytoplasms, showed that the fertility restoration of four CMS lines by T24 involved one nuclear gene, indicating that T24 was a result of the mutation of one nuclear gene. The mechanism of the restoration of CMS line by T24 was obviously different from other restorers such as Minghui 63 and 20964, which were shown to behave in two gene mode in fertility restoration. The discovery of the revertant T24 contributes to the understanding of CMS and fertility restoration of CMS in rice. The T24 and its parent II-32A may constitute a pair of near isogenic lines for the restoring gene, which should be valuable materials for molecular genetic analysis of CMS. 相似文献
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几个水稻不育系对白叶枯病的抗性 总被引:13,自引:0,他引:13
测定了8对不育系(A)和保持系(B)以及一些杂交稻组合对6个小种的40株白叶枯病菌的抗性,比较了不同类型不育系对6个小种群的抗性差异。结果表明,冈型、印尼水田谷型和大多数野败型不育系的抗性很差,BT型的抗性较高。菌株Ah28对冈46A和野败珍汕97A的致病力强。比较了6个恢复系(C)和8个杂交组合对不同小种的抗性程度。结果显示,杂交稻的抗病性主要受父本(恢复系)核基因的控制,但同时又受不育胞质的影 相似文献
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以典型籼稻和粳稻作对照,对湖南应用较广的几个两用核不育系进行叶绿体DNA的ORF100、ORF29-TrnCGCA片段长度以及rps16基因内含子和TrnTUGU-TrnLUAA转录间区2个片段序列进行比较研究。结果表明,株1S、陆18S、株77S、H628S、88S、白天鹭S、G0543S、G03S、1103S和W6154S的叶绿体DNA的ORF100、ORF29-TrnCGCA两片段的大小均与典型的籼稻一致,其他材料则与典型粳稻相同;叶绿体DNA碱基多态性较丰富的2个区域rps16基因内含子和TrnT UGU -TrnL UAA间区的测序后发现4个籼粳稻特异位点,这4个位点对两用不育系叶绿体籼粳属性的判断与ORF100、ORF29-TrnCGCA片段的结果一致。根据育出组合的数量和质量,带有粳型血缘细胞质的两用核不育系如准S、810S、、中心S、C185S和培矮64S等显现了一定的优势。研究结果说明,通过籼粳稻杂交选育具粳稻血缘的籼型不育系是提高杂交水稻产量的有效途径之一。 相似文献
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旨在了解并揭示不育系105A的花粉败育时期和细胞学特征,为进一步正确认识细胞质雄性不育系分子机制提供必要参考依据。采用石蜡制片法,对甘蓝型油菜杂交种‘青杂5号’的雄性不育系105A及其恢复系1831R的小孢子发生和花药发育过程进行观察,以确定其花粉败育的时期和细胞学特点。研究结果表明,在不育系105A花药败育过程中,一部分发生于造孢细胞时期,属于无花粉囊败育型;另一部分发生于单核晚期,属于单核败育型,其特点为单核晚期绒毡层细胞膨大向小孢子靠近,并逐步降解,其破裂胞质退化残余物侵入药室,与小孢子混合粘连在一起,甚至有些绒毡层细胞整块脱落,成为染色很深的团块状物质,占据药室一部分空间,最终小孢子降解,花药败育。 相似文献
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广亲和粳稻恢复系选育方法 总被引:1,自引:0,他引:1
广亲和粳稻恢复系的选育除采用WA型恢复与广亲和粳稻杂交选育和不同广亲和恢复系间杂交选育外,本研究提出以粳稻为父本杂交选育的4种办法:1、以型杂交稻F1为母本转育同质广亲和恢复系;2、以WA型下育系为母本筛选同质广亲和恢复系;3、以WA型广亲和不育系为母本,筛选同质广亲和恢复系;4、以同质广亲和恢复系为母本转育新的恢复系。用上述方法已育成02428等广亲和恢复系,并可同时恢复WA型和BT型胞质不育系 相似文献
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Identification of restorers and maintainers for developing basmati and non-basmati hybrids in rice, Oryza sativa 总被引:1,自引:0,他引:1
Twenty‐seven improved aromatic lines of germplasm and 18 non‐aromatic disease‐resistant genotypes of rice were test‐crossed with four cytoplasmic male‐sterile lines (IR 58025A, IR 62829A, PMS 3A and PMS 10A). Thirteen aromatic and 10 non‐aromatic genotypes were selected based on pollen fertility, and crosses were repeated to confirm sterility‐maintaining and fertility‐restoring ability. Genotypes were categorized as effective restorers (> 80% spikelet fertility), partial restorers (21‐79% spikelet fertility) and maintainers (< 1% spikelet fertility). The effective basmati restorers identified were Basmati 385, Chandan, P1031‐8‐5‐1, HKR 241‐IET‐12020, SAF Khalsa 7 and Karnal Local. The basmati maintainers identified were Basmati 370, Pusa basmati 1, P615‐K‐167‐13 and P1173‐4‐1. The frequency of restorers obtained was higher for the non‐aromatic than the aromatic basmati type. The performance of restorers varied with cytoplasmic male‐sterile (CMS) line, location and season of testing. The differential ability to restore fertility in the CMS lines that have the wild abortive (WA) cytosterile system could result from different nuclear backgrounds of the CMS lines. These restorers and maintainers possess acceptable grain dimensions, a desirable degree of aroma, volume expansion through linear kernel elongation and cooking quality characteristics of basmati rice. These genotypes will contribute to developing basmati hybrids and provide restorers and maintainers with acceptable key basmati quality characteristics. 相似文献