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1.
In Triticum durum Defs., gynogenesis was investigated on six genotypes, Cocorit, Isly, Jori, Oued Zénati, Sarif, issued from Morocco,and Cham1 from Syria. The experiments described here were made during two seasons (spring and summer) in which batches of 1,036 and 3,750 unpollinated ovaries were used. A 4 °C pretreatment was applied, during 7, 11 or 15 days and the A (modified Jähne's et al.,1991) and B (modifed San N?um's, 1976) induction media were compared. The spikes were harvested when microspores were at bi- or trinucleate stage. After the 4 °C cold pretreatment, they were sterilized, and the excised ovaries underwent the following phases and sequence of successive media. The A or B ‘induction’ media, induced cell divisions in the female gametophytes, and after 4 to 9 weeks in dark conditions, the swelling ovaries burst. The growing calluses were excised and transferred to 16 h. light onto a differentiation medium (dif); there generated shoots were then placed on a development (dev), followed by a rooting medium (r). The comparison of the two experiments showed that summer was the best season, for in vitro unpollinated ovary culture; this period corresponds to a growth of mother-plants during spring, while those developing in winter gave rise to lower scores. In Experiment 1 the best level of regenerated plants per 100 ovaries were obtained for Isly with 14.3% and for Oued Zénati with 10.1%. In Experiment 2, the best values were those of Isly with 21.8%, after a 7 day cold pretreatment and use of induction medium B, and of Cocorit with 18.1%. Jori, exhibited good results, in three define situations, with 17.1%, 16%, and 9.3%.Only Cham1 and Sarif showed very low scores or no plants. Jori remaining aside, for each genotype, the best values rose up from a specific treatment combination, as a very strong interaction was expressed between genotype, induction medium and cold pretreatment duration. After this ‘first phase’ of regeneration by ovary culture 150 haploid plants were obtained. When combining these results with other attempts, a total number of 191 green plants was regenerated, 90 for Isly, 74 for Jori, 19 for Cocorit, 7 for Oued Zénati and 1 for Cham1. In a ‘second phase’, permanent regenerating callus lines were obtained through subculture on dif medium. Depending on genotype, 2 to 9 transfers (up to one year for Jori) were performed, giving 507 regenerated plants. From direct regeneration and subcultures, a total of 698 plants were produced, all green and mostly haploid. Fertile doubled haploid plants were obtained, either spontaneously or by colchicine treatment, for all these genotypes. These results are of interest for breeders, who need pure lines for genotypes evaluation and for the creation of improved homozygous varieties.  相似文献   

2.
The root lesion nematode Pratylenchus thornei is widely distributed in Australian wheat (Triticum aestivum) producing regions and can reduce yield by more than 50%, costing the industry AU$50 M/year. Genetic resistance is the most effective form of management but no commercial cultivars are resistant (R) and the best parental lines are only moderately R. The wild relatives of wheat have evolved in P. thornei-infested soil for millennia and may have superior levels of resistance that can be transferred to commercial wheats. To evaluate this hypothesis, a collection of 251 accessions of wheat and related species was tested for resistance to P. thornei under controlled conditions in glasshouse pot experiments over two consecutive years. Diploid accessions were more R than tetraploid accessions which proved more R than hexaploid accessions. Of the diploid accessions, 11 (52%) Aegilops speltoides (S-[B]-genome), 10 (43%) Triticum monococcum (A m -genome) and 5 (24%) Triticum urartu (A u -genome) accessions were R. One tetraploid accession (Triticum dicoccoides) was R. This establishes for the first time that P. thornei resistance is located on the A-genome and confirms resistance on the B-genome. Since previous research has shown that the moderate levels of P. thornei resistance in hexaploid wheat are dose-dependent, additive and located on the B and D-genomes, it would seem efficient to target A-genome resistance for introduction to hexaploid lines through direct crossing, using durum wheat as a bridging species and/or through the development of amphiploids. This would allow resistances from each genome to be combined to generate a higher level of resistance than is currently available in hexaploid wheat.  相似文献   

3.
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4.
New sugarcane cultivars are continuously developed to improve sugar industry productivity. Despite this sugarcane crop models such as the ‘Sugar’ module in the Agricultural Productions System sIMulator (APSIM-Sugar) have not been updated to reflect the most recent cultivars. The implications of misrepresenting cultivar parameters in APSIM-Sugar is difficult to judge as little research has been published on the likely values of these parameters and how uncertainty in parameter values may affect model outputs. A global sensitivity analysis can be used to better understand how cultivar parameters influence simulated yields. A Gaussian emulator was used to perform a global sensitivity analysis on simulated biomass and sucrose yield at harvest for two contrasting sugarcane-growing regions in Queensland, Australia. Biomass and sucrose yields were simulated for 42 years to identify inter-annual variability in output sensitivities to 10 parameters that represent physiological traits and can be used to simulated differences between sugarcane cultivars. Parameter main effect (Si) and total effect (STi) sensitivity indices and emulator accuracy were calculated for all year-region-output combinations. When both regions were considered together parameters representing radiation use efficiency (rue), number of green leaves (green_leaf_no) and a conductance surrogate parameter (kL) were the most influential parameters for simulated biomass in APSIM-Sugar. Simulated sucrose yield was most sensitive to rue, sucrose_fraction (representing the fraction of biomass partitioned as sucrose in the stem) and green_leaf_no. However, climate and soil differences between regions changed the level of influence cultivar parameters had on simulation outputs. Specifically, model outputs were more sensitive to changes in the transp_eff_cf and kL parameters in the Burdekin region due to lower rainfall and poor simulated soil conditions. Collecting data on influential traits that are relatively simple to measure (e.g. number of green leaves) during cultivar development would greatly contribute to the simulation of new cultivars in crop models. Influential parameters that are difficult to measure directly such as transp_eff_cf and sucrose_fraction are ideal candidates for statistical calibration. Calibrating crop models either through direct observation or statistical calibration would allow crop modellers to better test how new cultivars will perform in a range of production environments.  相似文献   

5.
Environmental effects on genetic variation for chilling resistance were studied in nine cultivars and breeding lines (referred to as cultigens hereafter) of cucumber (Cucumis sativus L.). Five experiments were carried out in controlled-environment chambers to measure the effects of growth temperature, photoperiod, duration of chilling, light level during chilling, and watering frequency on chilling resistance of seedlings at the cotyledon and first true leaf growth stages. Significant interactions were found between cultigen and all environmental factors studied except for the photoperiod and watering frequency. Cultigen rank was affected by growth temperature before chilling, chilling duration, and light level during chilling, but shifts in rank were not consistent. Genetic variation was largest when the plants were grown at 22/18 °C, most pronounced after a chilling duration of 5 to 9 hours and a light level during chilling of 270 μmol·m-2·s-1. Variation was larger at the first true leaf stage than at the cotyledon stage. Differences among cultigens in chilling damage were largest 5 days after chilling. Therefore, it seems that testing for genetic variation in chilling damage can be restricted to one set of environmental conditions. We recommend the following conditions for screening cucumber for genetic variation in chilling resistance: grow the plants at 22/18 °C, under a 9-hour photoperiod with a 3-hour night interruption, water them once daily, subject them at the first true leaf stage to a chilling treatment of 7 hours at 4°C at a light level of 270 μmol·-2·s-1, and evaluate damage 5 days after treatment. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

6.
Deepwater rice possesses internode elongation ability to avoid drowning under deepwater conditions. Previous studies identified three QTLs regulating internode elongation ability on chromosomes 1, 3 and 12 using different populations. However, these QTLs only induce internode elongation in response to deepwater conditions from the 7-leaf stage and not during the early leaf stage. In this study, we detected two novel QTLs, qTIL2 and qTIL4 regulating deepwater response at the early leaf stage using an F2 population derived from the cross between NIL1-3-12 carrying the three QTLs regulating deepwater response in T65 (O. sativa ssp. japonica) genetic background and C9285 (O. sativa ssp. indica, deepwater rice). Plants of the BC2F2 population derived from NIL1-3-12/C9285 and the RILs of T65/Bhadua (O. sativa ssp. indica, deepwater rice) possessing these QTLs as well as the three QTLs previously identified also showed internode elongation during the early leaf stage. These results indicate that qTIL2 and qTIL4 regulate early internode elongation and function in coordination with the three major QTLs under deepwater conditions. The results presented here would not only help define the mechanism of deepwater response in rice but also contribute in the breeding of deepwater tolerant rice that is adapted to various water depths.  相似文献   

7.
Rust resistance in the sunflower line P386 is controlled by Pu6, a gene which was reported to segregate independently from other rust resistant genes, such as R4. The objectives of this work were to map Pu6, to provide and validate molecular tools for its identification, and to determine the linkage relationship of Pu6 and R4. Genetic mapping of Pu6 with six markers covered 24.8 cM of genetic distance on the lower end of linkage Group 13 of the sunflower consensus map. The marker most closely linked to Pu6 was ORS316 at 2.5 cM in the distal position. ORS316 presented five alleles when was assayed with a representative set of resistant and susceptible lines. Allelism test between Pu6 and R4 indicated that both genes are linked at a genetic distance of 6.25 cM. This is the first confirmation based on an allelism test that at least two members of the Radv/R4/R11/ R13a/R13b/Pu6 cluster of genes are at different loci. A fine elucidation of the architecture of this complex locus will allow designing and constructing completely new genomic regions combining genes from different resistant sources and the elimination of the linkage drag around each resistant gene.  相似文献   

8.
During the Snellius-II Expedition Lower Pilocene coral material was collected near Salayer, and Quaternary reefs were sampled on Ambon and Sumba. Coral collections from the Pliocene of Nias were also available for study. This new material is presented together with earlier data. Preservation potentials of different coral growth forms are reviewed. The absence of Acropora and Montipora from Quaternary coral faunae is striking. This is interpreted with the model of Potts (1983), on the disturbance by Pleistocene sea level fluctuations in the reef coral fauna. Diversification within both genera is apparently very recent, which may explain their complex taxonomy. Given the dominant role of Acropora and Montipora in many present day Indonesian reefs, these are better described as transitional assemblages of corals than as established coral communities.  相似文献   

9.
以375份小豆核心种质为试验材料, 利用从小豆及其近缘种SSR引物中筛选出的13对引物进行遗传多样性分析。检测结果显示, 小豆种质资源具有丰富的遗传多样性, 共检测到133个等位变异, 每对SSR引物检测到等位变异4~19个, 平均10.23个, 国内各省多态信息含量(PIC)平均为0.561, 多态位点比例(P)平均为93.523%。聚类结果表明, 小豆资源遗传关系与生态分区间有明显的联系, 且东北地区资源与中南部资源遗传关系较近。湖北、安徽、陕西3省资源的PIC较高, 且基本位于主坐标三维图的中心区域, 推断湖北、安徽、陕西是中国栽培小豆的起源地或多样性中心。该结果有助于更好地对小豆种质资源进行收集、保护和利用。  相似文献   

10.
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11.
Response of thermosensitive genic male sterility in rice to varying temperature situations was studied by using four TGMS lines. In three sets of maximum, minimum and their combined temperatures, it was observed that maximum temperature played a predominant role in influencing sterility/fertility of TGMS lines under the combined regimes. Expression of a TGMS gene was found to be influenced by the genetic background of the recipient lines. Exposure for more than 8 hours of 32 °C was found necessary to induce complete male sterility in indica TGMS lines: IR68945-4-33-4-14 and IR68949-11-5-31 while, more than 4 hours of such exposure was enough to induce sterility in case of their japonica donor Norin PL 12. Sudden interruption with 27 °C even for 2 hours under the sterility inducing regime of 32/24 °C could induce partial fertility in the line IR68945-4-33-4-14. However, the line ID 24 remained completely sterile even with 10 hours of interruption with 27 °C. An interruption with lower temperature of 27 °C for 4 hours for even one day induced partial fertility in IR68945-4-33-4-14. The period of four to eight days after panicle initiation was the stage most sensitive to temperature variations. Hybrid rice breeders need to develop numerous genetically diverse TGMS lines, which possess critical sterility inducing temperature of 28 °C and are not affected by sudden interruptions with a lower temperature for few hours daily for a couple of days. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

12.
Hybrid sterility hinders the transfer of useful traits between Oryza sativa and O. glaberrima. In order to further understand the nature of interspecific hybrid sterility between these two species, a strategy of multi-donors was used to elucidate the range of interspecific hybrid sterility in this study. Fifty-nine accessions of O. glaberrima were used as female parents for hybridization with japonica cultivar Dianjingyou 1, after several backcrossings using Dianjingyou 1 as the recurrent parent and 135 BC6F1 sterile plants were selected for genotyping and deducing hybrid sterility QTLs. BC6F1 plants containing heterozygous target markers were selected and used to raise BC7F1 mapping populations for QTL confirmation and as a result, one locus for gamete elimination on chromosome 1 and two loci for pollen sterility on chromosome 4 and 12, which were distinguished from previous reports, were confirmed and designated as S37(t), S38(t) and S39(t), respectively. These results will be valuable for understanding the range of interspecific hybrid sterility, cloning these genes and improving rice breeding through gene introgression.  相似文献   

13.
Ethylene biosynthesis in kiwifruit, Actinidia chinensis ‘Sanuki Gold’ was characterized using propylene, an ethylene analog, and 1-methylcyclopropene (1-MCP), an inhibitor of ethylene perception. In fruit harvested between a young stage (66 days after pollination) (DAP) and an early commercial harvesting stage (143 DAP), 2 days of exposure to propylene were sufficient to initiate ethylene biosynthesis while in fruit harvested at commercial harvesting stage (154 DAP), 4 days of propylene treatment were required. This observation suggests that response of ethylene biosynthesis to propylene treatment in kiwifruit declined with fruit maturity. Propylene treatment resulted in up-regulated expression of AC-ACO1, AC-ACO2, AC-SAM1 and AC-SAM2, prior to the induction of AC-ACS1 and ethylene production, confirming that AC-ACS1 is the rate limiting step in ethylene biosynthesis in kiwifruit. Treatment of fruit with more than 5 μL L?1 of 1-MCP after the induction of ethylene production subsequently suppressed ethylene production and expression of ethylene biosynthesis genes. Treatment of fruit with 1-MCP at harvest followed with propylene treatment delayed the induction of ethylene production and AC-ACS1 expression for 5 days. These observations suggest that in ripening kiwifruit, ethylene biosynthesis is regulated by positive feedback mechanism and that 1-MCP treatment at harvest effectively delays ethylene production by 5 days.  相似文献   

14.
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15.
Marker assisted backcrossing breeding has become one of the essential tools in transferring novel genes to adapted varieties and was employed to pyramid three blast resistance genes Pi1, Pi2 and Pi33 to a popular susceptible rice variety ADT43. Gene pyramiding process was facilitated by marker aided selection for both foreground as well as background genotype. Previously reported linked molecular markers were deployed to survey resistant and susceptible genotypes. In the BC3F1 generation four lines viz, AC-B3-11-7, AC-B3-11-36, AC-B3-11-57, AC-B3-11-83 were identified to be pyramided with three genes and subjected to background analysis and a genome recovery up to 95 % was observed and advanced to further generations. Morphological, yield and grain quality traits were significantly similar to ADT43. The introgressed lines with three gene combinations were highly resistant to the blast pathogen compared to genotypes with single genes and the susceptible checks under blast nursery screening at two epiphytotic locations; Coimbatore and Gudalur. The selected three gene pyramided backcross lines in the desirable background were advanced to obtain an improved ADT 43 with resistance to blast disease.  相似文献   

16.
以甘薯近缘野生种I. trifida (2x)为探针, 与I. trifida (4x) 2个株系“695104”和“697288”的体细胞染色体进行基因组荧光原位杂交, 结果显示, 2株系都与I. trifida (2x)有很近的亲缘关系, 但2株系的信号存在差异。“695104”几乎所有染色体整条都有均匀明亮的信号, 应为I. trifida (2x)基因组直接加倍而来;而 “697288”与“695104”不同, 虽然各条染色体也均有杂交信号, 但信号的区域与亮度有差异, 较为复杂, 可分为三种情况。第1种是整条染色体有均匀明亮的信号, 亮度与分布区域同“695104” , 有41条;第2种是几乎整条染色体有信号, 但亮度较第一种暗, 有14条;第3种为染色体部分区域有信号, 亮度较前二者更暗, 有5条。推测 “697288”是在加倍同时或之后又发生了基因组重组与部分变异。  相似文献   

17.
小麦品种中梁22抗条锈病基因的遗传分析和分子作图   总被引：8，自引：0，他引：8  
对中梁22/铭贤169杂交F2群体苗期抗条锈病鉴定及中国春单体系抗病基因的染色体定位发现, 中梁22携带1个显性(暂命名YrZhong22)和1个隐性抗病基因, 前者位于5B染色体。由中梁22´铭贤169的F2群体构建抗病、感病池, 用SSR标记结合集群分离分析法(BSA), 建立了与YrZhong22连锁的4个微卫星标记Xwmc289、Xwmc810、Xgdm116和Xbarc232, 并将YrZhong22定位于小麦5BL染色体。YrZhong22与相邻微卫星位点Xwmc810和Xgdm116的遗传距离分别是2.7 cM和4.4 cM。系谱分析及分子标记分析表明, YrZhong22可能是一个来自中间偃麦草的新抗条锈病基因。  相似文献   

18.
Antifungal activity against the pathogen, Botrytis cinerea, and a bioassay organism, Cladosporium cladosporioides, declined with advancing strawberry fruit maturity as shown by thin layer chromatography (TLC) bioassays. Preformed antifungal activity was also present in flower tissue. The fall in fruit antifungal compounds was correlated with a decline in natural disease resistance (NDR) against B. cinerea in planta. Crude extracts of green stage I fruit (7 days after anthesis) contained at least two preformed antifungal compounds (Rf=0.44 and 0.37) that were not present in white and red stage fruit. These compounds were shown with TLC reagent sprays to be neither phenolics nor alkaloids. Positive reactions to Ehrlich’s reagent suggested that Rf=0.37 was a terpene. Most antifungal activity was found in the achenes of green stage I fruit. However, antifungal activity was found in all tissue types (viz. pith, cortex, epidermis) of green stage I fruit. TLC bioassays revealed that all fruit stages yielded antifungal activity at the origin (Rf=0.00). The approximate area of fungal inhibition at the origin in green stage 1 fruit extracts was 1.87- and 1.73-fold greater than in white and red stages, respectively. TLC reagent sprays showed that the antifungal compound(s) at origin included phenolics. This observation is consistent with previous reports that phenolic compounds in strawberry fruit are inhibitory to B. cinerea.  相似文献   

19.
采用染色体步移技术分别克隆3个花生质体型酰基载体蛋白(ACP)基因的5′侧翼调控区序列,AhACP1、AhACP4和AhACP5基因5′上游序列分别为535、1400和1180 bp;利用5′RACE方法确定了这3个基因的转录起始位点,分别位于起始密码ATG上游–71、–92和–71 bp处。利用生物信息学软件分析了花生ACPs启动子区包含的主要调控元件,发现尽管花生AhACP4和AhACP5基因在根、茎、叶、花和不同发育期种子中的基本表达模式相似,但它们的启动子中包含各自特有的顺式元件,AhACP4启动子区包含根或芽顶端分生组织表达调控元件WUS,而AhACP5启动子区则含有侧芽萌动和伸展所需的多个关键调控元件E2FB、TELO BOX和UP1,推测它们的表达具有组织和发育阶段特异性。在进化上,花生AhACP4与拟南芥AtACP4可能为直系同源基因,但它们的表达模式产生了分歧,AhACP4为组成型表达,AtACP4主要在叶中表达;与AtACP4启动子相比,花生AhACP4启动子区中参与光调控相关元件明显减少。  相似文献   

20.
The impact of genetically modified canola (Brassica napus) on biodiversity has been examined since its initial stage of commercialization. Various research groups have extensively investigated crossability and introgression among species of Brassicaceae. B. rapa and B. juncea are ranked first and second as the recipients of cross-pollination and introgression from B. napus, respectively. Crossability between B. napus and B. rapa has been examined, specifically in terms of introgression from B. napus to B. rapa, which is mainly considered a weed in America and European countries. On the other hand, knowledge on introgression from B. napus to B. juncea is insufficient, although B. juncea is recognized as the main Brassicaceae weed species in Asia. It is therefore essential to gather information regarding the direct introgression of B. napus into B. juncea and indirect introgression of B. napus into other species of Brassicaceae through B. juncea to evaluate the influence of genetically modified canola on biodiversity. We review information on crossability and introgression between B. juncea and other related Brassicaseae in this report.  相似文献   

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