辣椒新品种驻椒21的选育

驻椒21是以辣椒雄性不育两用系AB0582为母本,以自交系B0318为父本选育而成的辣椒一代杂种。早熟,全生育182d(天)果实羊角形,果长19.2cm,果宽3.7cm,平均单果质量44.6g,青熟果黄绿色,每667m2产量3380kg左右,辣椒素含量26.2mg·kg-1,VC含量1040mg·kg-1。适宜早春保护地和春露地地膜覆盖栽培。     

Cre/loxP定位重组系统在植物雄不育和杂种优势中的利用研究

Cre—loxP是来源于噬菌体P1的一种位点特异性重组系统。目前，它已广泛应用于基因功能鉴定，动植物及微生物基因组的修饰以及基因的表达和调控。雄性不育系在杂种优势的利用中具有重要意义。本实验是以Cre—loxP系统调控细胞毒素基因barnase在植物雄性器官发育的特异时期在特异组织表达，从而达到控制植物育性的目的。1．在本实验中，通过PCR方法克隆了解淀粉芽孢杆菌Bacillus amyloliquefaciens的barnase基因，及其抑制因子barstar的DNA序列，同时，构建成功双元表达载体及基因枪转化载体，并已获得经分子险测呈阳性的小麦植株。2．osg6B是来源于水稻花药绒毡层的特异性的启动子，它在小孢子发育的四分体时期至单核花粉期在花药绒毡层中特异启动基因的表达，它具有较为严紧的时空特异性。以osg6B为启动子，构建了一组受控于Cre／loxP位点特异性重组系统的适用于基因枪法转化小麦的载体系统。其中，转不育基因(og6B—barnase)小麦植株生长正常，但开花后，花粉量明显减少，自交不能得到正常种子。进行花粉活力检测发现，转基因小麦大部分花粉表现为败育。花粉离体萌发试验表明，转不育基因小麦的花粉离体萌发率极低，几近败育。说明以osg6B驱动barnase在小麦花药中的表达可以导致雄性不育。3．以osg6B为启动子，构建了一组受控于Cre／loxP的用于控制双子叶植物育性的双元表达载体系统。以转cre基因的烟草作为受体，以含阻断序列的质粒农杆菌进行二次转化。二次转化株营养生长正常，但开花期花器官表现异常。具体表现为花瓣异常开裂或不开裂，花丝变短或粘连，花药提早萎蔫或异常开裂。推测这种现象的出现与启动子的组织特异性或barnase的渗露表达有关。4．二次转化株花粉染色因不同株系出现全部败育、部分不育和多数可育的情况。花粉离体萌发实验也得到了相似的结果。这说明通过筛选，利用Cre／loxP得到完全不育的植物株系是完全可行的。5．获得了9个barnase的突变体，初步推测第十四位氨基酸及第八十位氨基酸与核糖核酸酶活性有关。同时，发现barnase的第316位核苷酸序列为易突变位点，自然发生的突变多插入一个C，从而产生终止位点的改变。这或许会为今后barnase的克隆与利用提供一些参考。     

光敏、温敏核不育水稻核不育基因等位性及基因对数的研究

以光敏核不育系农垦58S及其衍生的光敏核不育系7001S、温敏核不育系W6154S、增矮64S，以及温敏核不育系安农S－1及其衍生的温敏核不育系810S、安湘S、香125S为材料进行相互杂交，在长日高温条件下观察F1的育性，根据其可育性和不育性确定核不育基因的等位性。结果表明：7001S、W6154S、培矮64S与核不育基因供体农垦58S之间有等位点的核不育基因；但温敏核不育系W6154S与培矮64S之间，不具等位点的温敏核不育基因。该结果说明光敏核不育系农垦58S至少存在一对光敏核不育基因和两对温敏核不育基因，而且各对温敏核不育基因可独立遗传，在夏季高温条件下其不育性得到充分表达。安农S－1与其衍生的不育系之间以及衍生的不育系与不育系之间都具有等位点的温敏核不育基因。农垦58S及衍生的核不育系与安农S－1及衍生的核不育系之间没有等位点的核不育基因。     

Genetic Control of Temperature-Sensitivity of Cytoplasmic Male Sterility (cms) in Chives (Allium schoenoprasum L.)

In earlier experiments with chives (Allium schoenoprasum L.) temperature-sensitive and temperature-insensitive cms plants could be selected. To obtain information about the site and nature of the genetic factor(s) responsible for the temperature sensitivity of the cms, temperature-insensitive and temperauire-sensitive cms plants were crossed with maintainers as well as with one another. In the progenies each genotype was cloned into two clone members, and these were examined concerning their male sterility under normal (20 °C/14 °C, day/night) as well as under constantly high temperatures (24 °C/ 24 °C). The results indicate that the temperature-sensitivity of the cms is controlled by a dominant nuclear gene “T”. This acts like a restorer gene at high temperatures and is ineffective at normal temperatures. Accordingly, important conclusions can be drawn with regard to the selection of temperature-insensitive cms-lines as well as to the propagation of the cmi-lines. The results are discussed in connection with the mitochondrial polypeptides probably responsible for the formation of the cms.     

甘蓝型油菜隐性核不育系ZWAB临保三交种与单交种的比较

利用甘蓝型油菜隐性核不育系ZWAB及临保系和恢复系分别配制了临保三交种、单交种进行组合的杂种优势比较,结果表明:临保三交种在抗性方面优于单交种,在经济性状及产量上与单交种相当。临保三交种完全可以替代单交种,从而节省了两系制种过程中初花期拔除50%可育株的环节,降低了劳动强度和成本,提高了制种产量和种子纯度。     

Seed productivity test of CMS lines of Japanese bunching onion (Allium fistulosum L.) possessing the cytoplasm of a wild species, A. galanthum Kar. et Kir.

In a previous study, we developed male sterile lines of Japanese bunching onion (Allium fistulosum L.) possessing the cytoplasm of a wild species, A. galanthum Kar. et Kir., by backcrossing. To evaluate seed productivity of the male sterile lines in practise, they were crossed with the male fertile line, cultivar 'Kujyo', using honeybees as pollinators under field conditions. The number of florets and seeds per inflorescence, seed set and seed germination of the material were investigated. Although variation was observed among the male sterile lines, there were several lines having seed productivity equal to cultivar 'Kujyo'. Our data demonstrate that the male sterile lines of A. fistulosum possessing the cytoplasm of A. galanthum are useful as seed parents for the commercial F seed production of A. fistulosum.     

Molecular genetic characterisation of the Asc locus of tomato conferring resistance to the fungal pathogen Alternaria alternata f. sp. lycopersici

The Alternaria stem canker disease of tomato is caused by the fungal pathogen Alternaria alternata f. sp. lycopersici and its host-selective AAL-toxins. Resistance to the pathogen and insensitivity to the toxins are conferred by the Asc locus on chromosome 3L. Sensitivity to AAL-toxins is a relative character; the toxins inhibit development of all tested tomato tissues but susceptible cultivars are much more sensitive than resistant cultivars. In addition to tomato, some other plant and animal species are sensitive to the toxins as well. The likely mode of action of AAL-toxins is interference with sphingolipid biosynthesis by specific inhibition of ceramide synthase activity. To molecularly isolate Asc, transposon tagging and positional cloning strategies are applied. As a first step, transposon insertions and restriction fragment length polymorphism (RFLP) markers are identified in proximity of the Asc locus. Subsequently, the transposons are used to inactivate Asc by insertion mutagenesis, and the RFLP markers are used to identify yeast artificial chromosomes (YACs) with tomato DNA inserts. Once an Asc-insertion mutant and/or a YAC encompassing Asc has been obtained, physical isolation and characterisation of Asc will be conceivable. Elucidation of the molecular role of Asc will illuminate the specificity of host recognition by Alternaria alternata f. sp. lycopersici.Abbreviations AAL-toxin Alternaria alternata lycopersici-toxin - A. a. lycopersici Alternaria alternata f. sp. lycopersici - Asc Alternaria stem canker - HST host-selective toxin     

Flowering behaviour,male sterility and berry setting in tetraploid Solanum tuberosum germplasm

Summary Six hundred and seventy six accessions of cultivated potato (Solanum tuberosum ssp. tuberosum) from 25 countries, were studied for flowering and fruiting behaviour under long days (12–14 h). Flowering intensity ranged from dropping of floral buds just after initiation to profuse blooming. The majority (58.3%) of the accessions bloomed profusely, though 20.4% of the accessions did not bloom at all. Weeks to flowering ranged from 6 to 15 and the majority (66.5%) of the flowering accessions bloomed within 8 to 9 weeks after planting. Duration of flowering ranged from 1 to 10 weeks and the majority (68.1%) of the flowering accessions bloomed for 1 to 4 weeks only. Twentythree per cent of the flowering accessions were completely male sterile. Maximum male fertility was 90% only. No berry setting was observed in 31.8% of the flowering accessions. Only 54.3 per cent of the accessions were found to be fertile in all respects and could be used both as male and female parents. Premature bud abscission was the major cause of sterility. Peru was the best source of profuse-flowering genotypes, Poland was the best source of early flowering genotypes and Mexico was the best source of long duration flowering and good berry setting genotypes. The results suggested that flower bud formation; the growth and development of mature flowers; weeks to flowering and duration of flowering are independent characters controlled by different genes of quantitative nature. Berry setting and duration of flowering were closely associated (r=0.95). Genetic as well as environmental factors interfered with the developmental process leading to flower production and berry setting at different times in different genotypes. The practical implications of these results for true potato seed production are discussed.Publication No. 1298, CPRI, Shimla.     

“Ch型”谷子显性核不育的遗传及其应用研究（Setaria italica）

通过对“Ch型”谷子显性核不育的遗传研究,证实“Ch型”的不育性与“澳大利亚谷”的细胞质无关,其育性是受两对显性连锁基因Ms-和Rf-上位互作控制的。其中Ms是显性不育基因,Rf是显性上位基因,当二者共同存在时,显性上位基因能抑制显性不育基因的表达,从而使不育表现可育。这种由杂交而来,并能找到“恢复系”的显性核不     

核不育芝麻小孢子败育机理的细胞学研究

核不育芝麻小孢子败育发生在四分体形成之后的无液泡小孢子期,败育在很短的时间内完成。败育前小孢子大量液泡化,其线粒体异常膨大与质体的基质化可作为小孢子开始败育的标志。败育小孢子缺少花粉外壁上的覆盖层。芝麻花药绒毡层的异常,包括有机物贮量的降低;细胞内含物的异位分布及迅速减少与消失;不能及时或缺乏分泌胼胝质