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普通小麦——华山新麦草异附加系的选育及细胞遗传学研究 总被引:5,自引:0,他引:5
利用普通小麦与华山新麦草(2n=14,NN)杂交与回产产生的七倍体杂种(AABBDDN,2n=49)再与普通小麦回交,即产生单体附加(2n=43)当以七倍体作父本时,产生单体附加的频率(24.2%)高于七倍体母本的频率(12.28%)单体了会加自交产生二体附加的频率为7.19%,不同附加系的细胞学稳定性有差异,并随着逐代选择而有所提高。 相似文献
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普通小麦和新麦草属间杂种的产生及细胞遗传学研究 总被引:17,自引:0,他引:17
进行了普通小麦和华山新麦草属间杂交,运用杂种幼胚培养技术,首次成功地获得了它们的属间杂种。F_1形态趋于中间型,均完全不育。F_1花粉母细胞预期类型(2n=28)的减数分裂中期Ⅰ平均染色体配对构型为26.72Ⅰ+0.62Ⅱ+0.01Ⅲ,后期Ⅰ和后期Ⅱ有落后染色体,多分体具大量微核。结果表明普通小麦和华山新麦草的染色体组间不存在同源或部分同源性。还观察到花粉母细胞异常减数分裂现象。用普通小麦回交,未获得回交后代。 相似文献
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普通小麦-百萨偃麦草(Thinopyrum bessarabicum)二体异附加系的选育与鉴定 总被引:10,自引:0,他引:10
为转移与利用百萨偃麦草耐盐、抗病等优良基因,用普通小麦中国春-百萨偃麦草双倍体与中国春杂交,通过染色体C-分带、分子原位杂交并结合减数分裂中期I的染色体配对分析,从回交后代中选育出一套小麦-百萨偃麦草二体异附加系。对这套异附加系进行的鉴定与分析表明,各附加系除添加了一对百萨偃麦草染色体外,小麦的21对染色体未见明显变化。各附加系所添加的百萨偃麦草染色体在减数分裂中期I配对基本正常,仅有少量单价体,其自交后代中外源染色体亦能正常传递。这说明所培育的这套二体异附加系在细胞学上已相对稳定,暂分别编号为DAJ1、DAJ2、DAJ3、DAJ4、DAJ5、DAJ6和DAJ7。各异附加系中百萨偃麦草染色体在小麦族中的部分同源群归属和百萨偃麦草耐盐抗病基因在染色体上的定位研究正在进行之中。 相似文献
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对小麦-华山新麦草附加系H20和代换系H1的抗病性及分子细胞遗传学进行了研究。结果 表明,H20和H1的体细胞染色体数目范围分别为42~44和40~42,2n=44和2n=42的细胞频率分别为58.33%和90%;花粉母细胞减数分裂中期Ⅰ,染色体构型分别为21.55Ⅱ十0.90Ⅰ和20.74Ⅱ十0.52Ⅰ,22Ⅱ和21Ⅱ的细胞频率分别为61.56%和86.18%;与中国春测交,21Ⅱ十1Ⅰ和20Ⅱ十2Ⅰ的细胞频率分别为70.14%和88.59%。用华山新麦草基因组DNA作探针进行原位杂交,结果显示H20和H1中均有2条华山新麦草染色体,他们的染色体构成分别为2n=44=42W 2N和2n=42=40W 2N。对全蚀病菌,H20表现近高度抗病性,H1表现中度抗病性。 相似文献
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对十倍体长穗偃麦草(Thinopyrum ponticum)与普通小麦杂交F1及其与普通小麦回交BC1F1的形态学和细胞学特性进行了分析。结果表明,长穗偃麦草与普通小麦‘兰考矮早八’衍生F1(‘兰考小偃麦’)的根尖细胞染色体数为56条;花粉母细胞减数分裂中期Ⅰ染色体构型平均值为19.81Ⅰ+15.78Ⅱ+0.75Ⅲ+0.59Ⅳ;基因组荧光原位杂交(GISH)显示,兰考小偃麦中含有35条完整的长穗偃麦草和21条小麦染色体。‘兰考小偃麦’/‘科育818’和‘兰考小偃麦’/‘Cp02-3-5-5’杂交F1的根尖细胞染色体数及其所遗传的长穗偃麦草染色体数分别为50~52和16~22条,且存在染色体易位;花粉母细胞减数分裂中期Ⅰ平均染色体构型为14.54Ⅰ+17.40Ⅱ+0.55Ⅲ+0.14Ⅳ,平均49.4%的细胞出现多价体(三价体或四价体)。这些材料为创造小麦-长穗偃麦草新种质奠定了基础。 相似文献
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利用荧光原位杂交和染色体C-分带技术对普通小麦-一华山新麦草的异代换系进行了研究。荧光原位杂交结果显示:异代换系H921—6—12和H924—3—4均含有2条华山新麦草的染色体。对这2个材料和华山新麦草进行染色体C-分带带型比较,结果认为:H921—6—12可能是普通小麦-华山新麦草的5A/N5^b代换系,H924—3—4可能是3D/N4^b代换系。 相似文献
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将大赖草种质转移给普通小麦的研究:VI.端体异附加系的选育与鉴定 总被引:1,自引:0,他引:1
利用根尖细胞有丝分裂中期染色体计数,花粉母细胞减数分裂中期1(PMC MI)染色体构型分析仪及C-分带,从普通小麦中国春与大赖草(LeymusracemosusLam.)杂种回交后代中,选育出两个端二体异附加系95G09,95G11和一个添加了一对大赖草第14号染色体和另一对端体的双重异附加系95G302(2n=44+2t),它们的PMC MI染色体配对构型分别为0.21个单价体(其中0.16个端 相似文献
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Variation of wheatgrass chromosomes in wheat-wheatgrass alien addition line "TAI-27"revealed by fluorescence in situ hybridization (FISH) 总被引:3,自引:0,他引:3
Transferofaliengenestowheatthroughchromosomeengineeringisoneoftheimportantwaystoimprovewheatgeneticbackground.Thebasicstepsofthisprocedurearefirsttotransferalienchromosomesintowheat,andthentointegratetheusefulgenesofalienchromosomesintowheatchromosome… 相似文献
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普通小麦—簇毛麦异附加系和异代换系的C—分带鉴定 总被引:8,自引:0,他引:8
用改良的C-分带技术鉴定南京农业大学细胞遗传研究室获得的普通小麦的簇毛麦V_2、V_3、V_4、V_6、V_7染色体异附加系和V_2、V_5异代换系,得到与N-分带和染色体配对分析一致的结果,并且由于C-分带可同时鉴别小麦全部21对染色体,鉴定出V_2异代换系中被代换掉的小麦染色体为1A。 相似文献
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Chromosome 2C from Aegilops cylindrica has the ability to induce chromosome breakage in common wheat (Tritivum aestivum). In the BC1F3 generation of the T. aestivum cv. Chinese Spring and a hybrid between T. aestivum-Leymus racemosus Lr.7 addition line and T. aestivum-Ae, cylindrica 2C addition line, three disomic translocation addition lines (2n = 44) were selected by mitotic chromosome C-banding and genomic in situ hybridization. We further characterized these T. aestivum-L, racemosus translocation addition lines, NAU636, NAU637 and NAU638, by chromosome C-banding, in situ hybridization using the A- and D-genome-specific bacterial artificial chromosome (BAC) clones 676D4 and 9M13; plasmids pAsl and pSc119.2, and 45S rDNA; as well as genomic DNA of L. racemosus as probes, in combination with double ditelosomic test cross and SSR marker analysis. The translocation chromosomes were designated as T3AS-Lr7S, T6BS-Lr7S, and T5DS-Lr7L. The translocation line T3AS-Lr7S was highly resistant to Fusarium head blight and will be useful germplasm for resistance breeding. 相似文献
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In order to transfer useful genes of Hordeum californicum into common wheat (Triticum aestivum L.), the T. aestivum c.v. Chinese Spring (CS)-H. californicum amphiploid was crossed to CS, and its backcrossing and self-fertilized progenies were analyzed by morpho-logical observation, cytological, biochemical and molecular marker techniques. Alien addition lines with two H. californicum chromo-somes were identified and their genetic constitution was characterized. STS-PCR analysis using chromosome 2B specific markers indi-cated that chromosome H3 of 1t. califomicum belongs to homoeologous group 2, and was thus designated 2H. SDS-PAGE showed that chromosome H2 of H. californicum belongs to homoeologous group 5, and was designated 5H. The CS-H. californicum amphiploid and the chromosome addition lines (DA2H and MA5H) identified were evaluated for powdery mildew (Erysiphe graminis f. sp. triticii) resis-tance in field. The preliminary results indicated that the amphiploid showed higher powdery mildew resistance than CS. However, chro-mosome addition lines DA2H and MA5H were highly susceptible to powdery mildew, indicating that major powdery mildew resistant genes of H. californicum should be located on chromosomes other than 2H and 5H. 相似文献
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桔梗雄性不育种质JXB-1的发现与鉴定 总被引:2,自引:0,他引:2
2006年在龙井市当地采集的3年生野生桔梗种源圃中发现雄性不育种质JXB-1个体,本研究对其生殖发育进行了进一步的实验验证。结果表明:JXB-1个体花的外观与正常的花比较无明显差异,但花药皱瘪;花药开裂,但无花粉粒散出,强行挤出来的花粉粒多数呈不规则型且无活力;套袋自交座果率为零,与30份不同桔梗种源杂交座果率为100%;经花药发育及小孢子发生过程观察,初步认为JXB-1花粉的败育主要发生在小孢子发育时期,JXB-1的绒毡层细胞过早解体,因而小孢子发育中途停止是败育的主要原因。用组织培养方法进行无性繁殖的JXB-1后代全部表现为雄性不育。初步研究结果表明JXB-1确属雄性不育,与其他种源有高度亲和力,可作为优良的育种材料。 相似文献
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Fang Kong Haiyan Wang Aizhong Cao Bi Qin Jianhui Ji Suling Wang Xiu-E Wang State Key Laboratory of Crop Genetics Germplasm Enhancement Cytogenetics Institute Nanjing Agricultural University Nanjing China 《Acta Genetica Sinica》2008,(11)
In order to transfer useful genes of Hordeum californicum into common wheat(Triticum aestivum L.),the T.aestivum c.v.Chinese Spring(CS)-H.californicum amphiploid was crossed to CS,and its backcrossing and self-fertilized progenies were analyzed by morphological observation,cytological,biochemical and molecular marker techniques.Alien addition lines with two H.californicum chromosomes were identified and their genetic constitution was characterized.STS-PCR analysis using chromosome 2B specific markers indica... 相似文献