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国家自然科学基金(30771518)

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Male Sterile Lines of Zinnia elegans and Their Cytological Observations被引量:3
2008年
In order to find out a new pathway for utilizing heterosis of Zinnia elegans and accelerate breeding process, the mechanism of anther development of a male sterile line was explored. Backcross, sibmating, selling of fertile plants and testcross with inbred lines were analyzed and identified in the field, and cytology was observed. Recessive nucleus male sterile line AH209AB capable of being a maintainer was obtained by successive backcrosses with male sterile plants and fertile F1 plants as male parents. Cytological and anatomical studies indicated that: (1) The wall of normal anther was constituted of four layers of cells such as epidermis, powder chamber wall, middle level and tapetum cells. The process in meiosis of pollen mother cell in Zinnia elegans was normal and cytoplasm divided simultanously. Mature pollen grain was tricellular type. (2) The petal of male sterile plant degraded as a thread-like structure, the stamens were villiform in appearance and no pollens were formed. The result showed that the anther of male sterile plant no longer proceed to differentiate spore mother cell and the pollen sac after the formation of the tissue of sporogenous cells, there was no evident boundary between tapetum cell, middle lamella and inner wall of PMC, tapetal cells did not develop from the very beginning. So the abortion type was completely structural male sterility. The male sterile line belongs to non-sporange male sterile type and is of great use in F1 seeds production.
YE Yao-mei HU Qiu-shi CHEN Tian-hua BAO Man-zhu
关键词:CYTOLOGY
Construction and Analysis of Suppression Subtractive cDNA Library from Fertile Disk Floret Buds of Zinnia elegans
2012年
In order to isolate genes related to anther development and understand molecular basis of male sterility,cDNA library of Zinnia elegans was constructed using suppression subtractive hybridization(SSH) approach.672 different expressed clones were selected from the fertile disk floret buds.PCR results showed that cDNA inserts were ranged from 100 to 750 bp.303 positive clones screened by dot-blot hybridization were sequenced.273 out of 303 sequenced clones produced readable sequences;these sequences represent 87 non-repetitive sequences.The homology alignment showed that 76 expressed sequence tags(ESTs) had functional annotations in GenBank,the other 11 ESTs without any homology to the known gene.In addition,87 ESTs were divided into 17 groups according to MIPS of Arabidopsis thaliana database.Sequence data from the cDNA library have been deposited with the GenBank under the accession numbers GT067016-GT067085.As an important result in this study,7 genes related to anther development were isolated.Results from semi-quantitative RT-PCR showed 6 genes were expressed only in disk florets of fertile plants compared with that of male sterile plants.These ESTs obtained provide important clues for further isolation and identification of fertility-related genes in Z.elegans.
PANG Rui-huaMA Guang-yingLOU Xue-yuanBAO Man-zhuYE Yao-mei
百日草雄性不育系的获得及其细胞学观察被引量:8
2008年
【目的】获得百日草雄性不育系,并探索其花药发育机制,为百日草杂种优势的利用提供一条新途径。【方法】采用自交F2代出现的不育材料连续回交获得的不育系再进行兄妹交、可育株自交,结合与多个自交系测交进行不育类型鉴定,并对其细胞学进行研究。【结果】获得了百日草深红色单隐性雄性不育两用系AH209AB。正常可育的花药,其药壁由4层细胞构成,即表皮、药室内壁、中层和绒毡层;花粉母细胞减数分裂过程中的胞质分裂为同时型;成熟花粉为三细胞型。雄性不育株花瓣退化或丝状,雄蕊退化成丝状,内无花粉,外观呈绒毛状;花药在造孢细胞组织形成后,没有继续分化产生药壁结构、花粉母细胞及其花粉,为完全的结构性雄性不育类型。【结论】该雄性不育系属于无花粉囊型不育系,在F1代种子生产上具有重要的利用价值。
叶要妹陈天花胡秋实包满珠
关键词:百日草雄性不育花药发育细胞学
百日草属EST-SSR信息分析及其雄性不育两用系鉴别引物筛选被引量:4
2017年
百日草雄性不育在F1代杂交育种中应用广泛,建立百日草雄性育性EST-SSR分子标记,为百日草分子标记辅助育种奠定科学基础。本研究通过分析NCBI数据库中百日草属EST序列20 667条,进行EST-SSR信息的分析。采用20μL红酶PCR反应体系,以百日草雄性不育两用系MJ16AB的DNA为模板,筛选引物。结果获得622条重复基元不少于5次且重复序列长度≥12 bp的SSR,其中二、三核苷酸出现次数最多的是AT/TA、CTA/GAT,分别占总数的9.5%、10.6%。随机合成的136对引物中,引物28、30、33、69和Ze M63在百日草可育和不育两池间扩增出清晰且稳定的差异性条带。本试验验证了基于百日草属EST数据开发SSR分子标记的可行性,筛选出的5对多态性引物可用于建立百日草雄性育性分子标记。
胡妙秦美姣李娟叶要妹
关键词:百日草雄性不育两用系EST-SSRPCR反应体系引物筛选
利用RAPD和ISSR分析百日草自交系间的种质遗传多样性被引量:6
2008年
首次运用RAPD与ISSR技术分析了百日草20个自交系的种质遗传多样性.结果表明:从供试材料中147条RAPD引物和44条ISSR引物筛选到具有多态性的RAPD引物12条,ISSR引物9条.RAPD引物共扩增出147条带,多态性位点数为100,多态性位点比率为68.03%,平均多样性指数为0.3559,有效等位基因数为1.4169;ISSR引物共扩增出128条带,多态性位点数为97,多态性位点比率为76.38%,平均多样性指数为0.4013和有效等位基因数为1.4728.试验表明,RAPD、ISSR及两种分子标记整合后的结果较为相似,呈极显著的正相关.聚类结果将20个自交系基本分为2类:一类群来源虹越种子集团公司;另一类群来源甘肃酒泉种子集团公司,分类与原产地相关.RAPD与ISSR标记是研究百日草种质遗传多样性有效的工具,在分析百日草的亲缘关系特别是系谱关系时,ISSR是一种多态性和重复性优于RAPD的分子标记.两种分子标记整合后既能鉴定出自交系的系谱先后关系,也能反应来源相同自交系的亲缘关系.
叶要妹
关键词:百日草自交系RAPDISSR种质遗传多样性
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