普通小麦×中间偃麦草杂种配子及后代类型形成途径的细胞遗传学研究

配制了(普通小麦×中间偃麦草)杂交组合15个。在回交结实的 F₁植株 PMC中均观察到染色体完全呈单价体构型。单株染色体分析表明,获得的32个 BC₁单株基本上包括了2n=42至2n=63的各种过渡类型,其中2n=63植株占37.5%。而且81.25%的植株在2n=59～63的范围内。显然,F₁产生的可育雌配子主要是染色     

玉米抗大斑病遗传及其育种的研究

用多基因抗大斑病自交系进行抗性遗传研究指出,双亲病级平均值,和 F₁病级呈高度显著正相关(r=0.925),与 F₂出现高抗株率(%)为极显著负相关(r=-0.914);F₁病级和 F₂高抗株率亦呈极显著负相关(r=-0.766)。单显性基因(Ht₁)自交系,在不同的遗传背景中,对 F₁传     

玉米果穗结实习性遗传特点及其SSR标记分析

为了探明玉米果穗结实习性的遗传特点,选用有限结实特点的lx01-3和无限结实特点的wx04-1玉米自交系进行杂交。在30 000株 hm^-2的种植密度下,分析了两亲本自交系及其F₁、F₂、BC₁和BC₂植株的果穗结实特性。结果表明,F₁代植株的果穗均为无限结实类型,无限结实类型为显性;无限结实与有限结实类型的分离比例,在F₂群体中符合15∶1,在BC₁群体中符合3∶1,表明玉米果穗的结实习性可能是由2对存在重叠作用的基因决定的。利用F₂分离群体分组法进行SSR标记分析发现,引物bnlg1601和umc1663扩增的特异产物带与控制结实习性的基因存在密切的连锁关系,进而将控制玉米果穗结实习性的2个基因初步定位于玉米的第３和第8染色体。     

冬性与春性小麦的杂种性状表现和选择

冬小麦与春小麦的杂种 F₁春性是显性,F₂冬、春性分离,其中春性占大多数;F₃—F₄基本稳定。F₁越冬率比春性亲本明显提高;F₃出现越冬性较好的类型。春性和冬性小麦杂交可以获得春播正常抽穗,而秋播越冬较好的类型。杂种 F₁抽穗期比春性亲本晚;F相似文献   

玉米抗南方型锈病基因共分离分子标记的研究

本文以玉米(Zea mays L.)抗南方型锈病自交系P₂₅和感病自交系F₃₄₉的F₁与F₃₄₉回交,并连续回交所得BC₅代的F₃₄₉抗病近等基因系（nearly isogenic lines,NILs）为材料,以RGA（resistance gene analogs）的方法,在抗病自交系中克隆出一条321 bp的特异性DNA条带。根据序列比对的结果,设计出新的引物作为分子标记,在96株BC₇、BC₄F₅NILs及其亲本和杂种F₁群体上进行鉴定,其中94株的田间抗感结果与分子检测结果一致,选择的有效率达97.9%。此标记扩增效果清晰,可重复性强,在抗玉米南方型锈病的分子标记辅助育种研究中有应用价值。     

优质蛋白玉米籽粒性状的遗传效应

选用8个胚乳性状差异显著的优质蛋白玉米(QPM)自交系, 采用Griffing I交配设计组配, 通过对亲本、F₁和F₂的鉴定, 探讨主要籽粒性状的遗传效应和杂种优势, 为有效利用热带硬质QPM种质改良、扩增我国温带QPM种质以及QPM籽粒性状改良和硬质QPM品种选育提供依据。结果表明, 籽粒百粒重、百粒体积、胚乳修饰度和籽粒密度在F₁和F₂代都表现一定的正向杂种优势; 胚乳修饰度在F₁代存在正反交差异, 母体效应明显; 4个性状的F₂代表型值与中亲值的相关性最大; 百粒重和百粒体积主要受母体效应控制, 基因效应以显性效应为主; 胚乳修饰度主要受种子直接效应控制, 基因效应以加性效应为主; 籽粒密度主要受母体效应控制, 基因效应以加性效应和显性效应同等重要。这4个籽粒性状的细胞质效应均较小, 主要受核基因控制。     

水稻三明显性核不育基因的初步鉴定

2001年在福建省尤溪县西城镇凤元村进行两系核不育系育性鉴定时, 在SE21S/Basmati 370组合编号为S221的800多株F₂代分离群体中发现1株与其他不育株的花粉败育形态不同的植株。经测交、回交、姐妹交的后代育性分离调查, 不育株与可育株呈1︰1分离, 以不育株为母本与普通品种配制杂交组合, 其后代育性呈1︰1分离, 可育株后代分离不出不育株, 表明S221不育性受核内1对显性不育基因控制。     

玉米种子休眠性的数量遗传分析

运用植物数量性状主基因+多基因混合遗传模型多世代联合分析的方法,对普通玉米自交系R08与A318杂交组合的P₁、P₂、F₁、F_2:3、B_1:2和B_2:26个世代群体的种子休眠性进行了分析。结果表明,它们的遗传符合1对负向完全显性主基因+加性-显性多基因模型。在F_2:3、B_1:2和B_2:2三个家系世代,主基因方差分别为0.9260、1.4176和0.5863;多基因方差分别为0.1184、0.1022和0.4623。主基因加性效应值为1.2172,显性效应值为-1.2172;多基因加性效应值为1.5028,显性效应值为1.4334。主基因遗传率在F_2:3、B_1:2和B_2:2三个分离家系群体中为44.8%~79.65%,多基因遗传率为5.74%~35.33%。其中,主基因遗传率在B_1:2世代中最大,为79.65%。     

玉米抗丝黑穗病的基因效应

利用2个抗玉米丝黑穗病自交系（齐319和Mo17）与2个感病系（E28和黄早四）,组配4个抗感杂交组合。2004年,对4个组合的亲本、F₁、F₂、BCR（F₁与抗病亲本回交1代）和BCS（F₁与感病亲本回交1代）6个世代群体分别在北京和黑龙江进行丝黑穗病的人工接种鉴定,采用世代平均值分析玉米抗丝黑穗病的遗传特点。研究表明,各杂交组合的抗病性均含有显著的加性效应,其中3个组合有显著的显性效应。不同杂交组合的抗病遗传模式表现不同,用感病亲本E28组配的2个组合（齐319×E28）和（Mo17×E28）的抗病性基本符合加性-显性遗传模型;而用另一个感病亲本黄早四组配的组合（齐319×黄早四）和（Mo17×黄早四）的抗病性存在明显的上位性效应。这说明玉米对丝黑穗病的抗性呈现较复杂的遗传模式。因此,在抗玉米丝黑穗病育种中既要重视对自交系抗病水平的鉴定,也要加强杂种F₁的合理组配及抗病性评估。     

春麦杂种后代抽穗期变异的初步观察

本试验里对春麦杂种后代抽穗期的变异进行了初步的观察与研究。结果证明,双亲与杂种 F₁代的相关系数为0.8655,与 F₂代的相关系数为0.8890,均表现极显著地高度正相关。据四年用41个组合估算的广义遗传力平均为61.2%,不同组合间遗传力变幅为44—85%。在324个杂种 F₁代组合中,超早亲和同早     

Genetic stability and maintenance of Raphanus sativus lines with an added Brassica rapa chromosome

The genetic stability and maintenance of Raphanus sativus‐Brassica rapa monosomic chromosome addition lines (a‐h‐types MALs, 2n = 19, BC₂), developed by backcrossing the synthesized amphidiploid Raphanobrassica (Raphanus sativus × Brassica rapa, 2n = 38, RRAA) with R. sativus cv. ‘Shogoin’ (2n = 18, RR), was investigated. Transmission of the added alien chromosome through selected smaller seeds (SSS) and the inheritance of morphological traits and random amplified polymorphic DNA (RAPD)‐specific markers together with meiotic chromosome configuration and seed fertility were also investigated for three successive generations (BC₃ to BC₅). The distinctive traits and the RAPD‐specific markers of the eight types of MAL were substantially inherited and stably maintained throughout three generations, although a few variant plants (2n =18) resembling MALs (2n = 19) and hyperploidal plants (2n = 26 and 2n = 37) were generated in the earlier generations of BC₃ and BC₄ in comparison with BC₅. The average transmission rates for three generations ranged from 26% for both the b‐type and the d‐type to 44% for the e‐type through SSS. On the other hand, the transmission rates through randomly selected seeds (RSS) were lower, ranging from 6.5% for the f‐type to 23.5% for the b‐type. In meiosis, more than 90% of PMCs showed the 9II +1I pairing configuration at metaphase I throughout three generations. For seed fertility, when backcrossed with the radish cv. ‘Shogoin’, the values were approximately 180% to 500% with the mode around 300% with the seed harvested from a pod increasing with the advancing generations. Genetic recombination between the radish chromosomes and the added chromosome is probably rare, suggesting that the added chromosome is mostly maintained unaltered in the background of the radish genome.     

Synthesis and sterility of raphanobrassica

Summary The synthesis of Raphanobrassica (2n=36, rrcc) from Raphanus sativus (2n=18, rr) and Brassica oleracea (2n=18, cc) is described a) by colchicine treatment of diploid hybrids; b) by crossing autotetraploid froms of the parent species.The variation within R. sativus and B. oleracea suggests that a range of morphologically distinct Raphanobrassica forms may be created, some of which may have agronomic potential and in particular, it is hoped, Plasmodiophora resistance.Inter-generic hybrids were readily obtained from crossing the parental species at both 2x and 4x chromosome levels, but only with R. sativus as female parent.Details are given of the morphology, fertility and chromosome behaviour of both diploid F₁ R. sativus × B. oleracea hybrids and of the amphidiploid Raphanobrassica.Synthesized Raphanobrassica plants proved, in general, highly sterile. Some aneuploids resulted from 4x R. sativus × 4x B. oleracea crosses but most progeny were euploid and showed almost regular chromosome association. A number of stunted, deformed plants were obtained from both 2x and 4x crosses. Vigour, fertility and aneuploidy appeared unconnected in the amphidiploid.Previous work on Raphanobrassica is reviewed. It is concluded that the extremely low fertility encountered in the present study is more likely to be the result of genic imbalance than to cytological anomalies which appear to be of lesser significance.     

Inheritance of siliqua locule number and seed coat colour in Brassica juncea

The inheritance of siliqua locule number and seed coat colour in Brassica juncea was investigated, using three lines each of tetralocular brown seeded and bilocular yellow seeded. Three crosses of tetralocular brown seeded × bilocular yellow seeded lines were attempted and their F₁, F₂ and backcross generations were examined for segregation of these two traits. Brown seed colour and bilocular siliqua characters were found to be dominant over yellow seed and tetralocular siliqua, respectively. Chi‐square tests indicated that each trait is controlled by different sets of duplicate pairs of genes. Bilocular siliquae or brown seeds can result from the presence of either of two dominant alleles, whereas tetralocular siliquae or yellow seeds are produced when alleles at both loci are recessive. A joint segregation analysis of F₂ data indicated that the genes governing siliqua locule number and seed colour were inherited independently.     

Inheritance of siliqua orientation and seed coat colour in Brassica tournefortii

The inheritance of siliqua orientation and seed coat colour in Brassica tournefortii was investigated using four genotypes varying in these two characters. The F₁, F₂ and backcross generations of two crosses were used for studying the segregation pattern of the traits. The plants were classified for seed colour as having brown or yellow seeds and for siliqua orientation as having upright, semi‐spread or spread siliqua. Seed colour was found to be under monogenic control with brown being dominant over yellow. Siliqua orientation was under digenic polymeric gene action: upright siliqua was produced by the presence of two dominant genes and spread siliqua by two recessive genes. The absence of even a single dominant gene resulted in a third type of siliqua orientation, semi‐spread siliqua.     

Production and characterization of Raphanus sativus-Brassica rapa monosomic chromosome addition lines

Breeding of Raphanus sativus‐Brassica rapa monosomic chromosome addition lines (MALs, 2n = 19) was carried out by backcrossing the synthesized amphidiploid line, Raphanobrassica (R. sativus×B. rapa, 2n = 38, RRAA, line RA89) with R. sativus cv. ‘Shogoin’ (2n = 18, RR). In the first cross of Raphanobrassica× radish, four sesquidiploidal BC₁ plants (2n = 28, RRA, RA89‐36‐1, RA89‐31‐1, RA89‐31‐2, RA89‐31‐3) were successfully developed. In these plants, the chromosome configurations of 9II + 10I and 10II + 8I were observed frequently at first metaphase (MI) of meiosis in pollen mother cells (PMCs). The RA 89‐36‐1 plant produced many seeds in the reciprocal backcrosses with radish. About 50% of the BC₂ plants obtained from the cross of RA89‐36‐1 plant × radish were 2n = 19 plants, followed by 2n = 18 plants (24%) and 2n = 20 plants (19%). In the reciprocal cross, 2n = 19 plants were also developed at the rate of 40%. From analysis of specific morphological traits, 2n = 19 plants were classified into eight types (a‐h). When 25 selected primers were used in polyacrylamide gel electrophoresis, random amplified polymorphic DNA (RAPD) markers derived from B. rapa for each type of MAL were detected in numbers between three for e‐type and 16 for b‐type. RAPD markers specific for each type alone were from one (OPE 05‐344) for h‐type to nine for b‐type. In the g‐type, no marker specific to this type alone was observed. However, 19 bands were common between at least two types. These MAL plants exhibited predominantly the chromosome configuration of 9II + 1I at MI of PMCs, pollen and seed fertility being the same level as the radish cv. ‘Shogoin’. From the morphological traits and DNA markers, eight different MAL types among 10 expected were identified.     

Cytogenetics of Brassica juncea×Brassica rapa hybrids and patterns of variation in the hybrid derivatives

Interspecific hybridization is an important tool to elucidate intergenomic relationships, transfer characters across species and develop synthetic amphidiploids, and it has been widely applied for improving Brassicas. The objective of the present study was to create genetic variability in Brassica through interspecific hybridization. Crosses between Brassica juncea (AABB, 2n= 36), and Brassica rapa (AA, 2n = 20) vars toria, yellow sarson, and brown sarson were attempted, and the hybrid derivatives were advanced to the F4 generation. Hybrids were obtained from the crosses B. juncea× toria and B. juncea× yellow sarson. The F₁ plants were vigorous and intermediate to the parents in many morphological traits. The meiotic study of AAB hybrids showed 10 II + 8 I in the majority (71.8%) of cells analysed. A maximum of 12 and a minimum of seven bivalents were also observed in a few cells. The occurrence of multivalent associations (trivalents to pentavalents) at diakinesis/metaphase I and a bridge‐fragment configuration at anaphase I were attributed to homoeology between A and B genomes. A high percentage of plants resembling B. juncea was observed in the F₂ generation. Transgressive segregation in both directions was found for plant height, primary branches, main raceme length, siliquae on main raceme, siliqua intensity, seeds per siliqua and seed yield. There were significant differences for the 14 characters in the F₄ derivatives. Moderate to high estimates of phenotypic and genotypic coefficients of variation, broad‐sense heritability, and expected genetic advance were found for seed yield, 1000‐seed weight, siliquae per plant, seeds per siliqua and days to flowering. Intergenomic recombination, reflected as wide variation in the hybrid progenies, permitted the selection of some useful derivatives.     

Production of intergeneric hybrids between Raphanm and Moricandia

Intergeneric F₁ hybrids between Raphanus sativus (2n = 18, RR) and Moricandia arvensis (2n = 28, MaMa) have been produced through ovary culture followed by embryo culture, when M. arvensis was used as a pistillate parent. Six BC₁ plants were also obtained through ovary culture followed by embryo culture in the backcross of an amphidiploid F₁, hybrid with R. sativus cv. 'Pink ball'. Two BC₁ plants were ses-quidiploids (2n = 32, MaRR), and the other BC₁, plants were hyperploid with 2n = 55, having MaMaRRR genomes. BC₂, seeds were obtained by conventional pollination in the successive backcross of two sesquidiploid BC₁, plants with R. sativus cv. 'Pink ball'. Their seed set percentages were 12.7% and 17.0%, respectively. These novel hybrid plants and derived progenies may be valuable materials for the genetic investigation and breeding of Brassiceae , including R. sativus.     

Carbohydrate Metabolism in the Siliqua Relating to Oil-filling in Mustard Seeds

Developing siliquas on the mustard inflorescence were sampled at basal, middle and apical positions and the changes in free sugars and starch in pod wall and seed vis-á-vis oil-filling in the seeds were studied. The dry matter and oil content per seed and pod wall was highest at initial stages in apical followed by mid-development stages in middle and late development stages in basal positions. The oil percentage m the pod wall decreased with the period of siliqua development. The phase of rapid oil filling in the seeds varied from 20 to 40 DAF (days after flowering) in basal to 10 to 30 DAF in middle and 10 to 20 DAF in apical positions. The content of starch and total soluble sugars (% dry weight basis) decreased in the seeds as well as pod walls but showed accumulation on per seed basis with a maximum at 20, 30 and 40 DAF while on pod wall basis, the maxima of total soluble sugars was at 20, 20 and 40 DAF in apical, middle and basal position respectively. In the pool of total soluble sugars, the proportion of non-reducing sugars was predominant. The activity of invertase (EC 3.2.1.26) declined while those of a-amylase (EC 3.2.1.1) and β-amylase (EC 3.2.1.2) showed maximum values in the seeds as well as pod wall during the phase of rapid oil-filling in the seeds. The results suggested that ontogeny and duration of seed development vis-á-vis the environmental conditions played an important role in lipid biosynthesis in mustard seeds.     

Molecular markers for yield components in Brassica juncea – do these assist in breeding for high seed yield?

A population of 112 F₁-derived doubled haploid lines was produced from a reciprocal cross of Brassica juncea. The parents differed for seed quality, seed color and many agronomic traits. A detailed RFLP linkage map of this population, comprising 316 loci, had been constructed, and was used to map quantitative trait loci (QTL) for seed yield and yield components, viz. siliqua length, number of seeds per siliqua, number of siliques per main raceme and 1000-seed weight. Stable and significant QTLs were identified for all these yield components except seed yield. For yield components, a selection index based on combined phenotypic and molecular data (QTL effects) could double up the efficiency of selection compared to the expected genetic advance by phenotypic selection. Selection indices for high seed yield, based on the phenotypic data of yield and yield components, could only improve the efficiency of selection by 4% of the genetic advance that can be expected from direct phenotypic selection for yield alone. Inclusion of molecular data together with the phenotypic data of yield components in the selection indices did not improve the efficiency of selection for higher seed yield. This is probably due to often negative relationships among the yield components. Most of the QTLs for yield components were compensating each other, probably due to linkage, pleiotropy or developmentally induced relationships among them. The breeding strategy for B. juncea and challenges to marker assisted selection are discussed.     

Image analysis measurements and repeatability estimates of siliqua morphological traits in Brassica campestris L

Summary The repeatabilities of six traits; peduncle, pod, beak, and total siliqua length, seed number/siliqua and seed mass/siliqua were estimated for the random-mating CrGC-1 Brassica campestris L. population. All length measurements were made using a fast digital image analysis technique. Beak, pod, and total siliqua length showed the highest repeatabilities of all six traits (0.73, 0.63, and 0.63, respectively). Both pod and total siliqua length were highly correlated with both seed number and seed mass/siliqua. These results suggest that these siliqua-related morphological traits could be used as indirect indices of selection in breeding for improved seed yields in Brassica campestris L.