共查询到20条相似文献,搜索用时 15 毫秒
1.
The endosperm calli were induced on MS basic medium supplemented with lppm 2,4-D, 0.5ppm KT and 5% sucrose. The medium which contained lppm BAP, 0.1ppm NAA and 2% sucrose was used for cell suspension culture. In suspension cell culture, amitosis of cleavage division of nucleus have been observed after 5 days of culture. First the nuclear membrane and nucleolus disappeared. The crevice appeared in the center of the nucleus, and the nucleus divided into two daughter nuclei of similar size and each with a nucleolus. The daughter nucleus resembled an eye in shape. Following the emergence of cell wall, the two new unequal cells were produced. Such amitotic division proceeded repeatedly until the callus developed and eventually plantlet regenerated. 相似文献
2.
石刁柏已形成细胞的幼嫩胚乳,接种在附加有不同浓度的生长素(NAA)和细胞分裂素(BA)的 MS 培养基上,获得了愈伤组织。愈伤组织的诱导频率随生长素的浓度不同而异,可达65.9—83.1%。将胚乳愈伤组织转移到降低了生长素浓度或只含有低浓度生长素的分化培养基上,可陆续分化芽、根、芽丛和少量胚状体,个别的芽和胚状体能发育成小植株。切取1.5—5cm 长的芽,接种在诱导根的培养基上,或在 IBA50ppm 溶液中浸泡2小时,转移到 MS 基本培养基上,部分芽能生根形成完整植株。 相似文献
3.
The endosperm callus has been induced from the young endosperm of Asparagus officinalis L. on the MS supplemented with auxin. The induction frequency of callus amounts to 65.9%–83.1%. When the callus was transferred to the medium supplemented with lower concentration of NAA 0.1 ppm or containing BA 1 ppm and NAA 0.5 ppm, the differentiation of shoots, roots and a few embryoids began to occur. A few calluses and embryoids can develop into plantlets. The chromosome number in the cells from the same root tip and shoot apex of endosperm plantlet is very unstable. They can be euploids (n=10, 2n=20, 3n=30, 4n=40). or aneupl0ids (n=6, 7, 17, 25, 53). 相似文献
4.
This paper describes the construction and characterisation of a cDNA library from wheat endosperm tissue during the early stages of grain filling. Developing wheat endosperm tissue was characterised with respect to standard measures including dry weight, cytological appearance and timing of expression of major sources of mRNA such as the seed storage protein genes. In addition, the full complement of proteins present at mid-endosperm development was examined using 2D-electrophoretic techniques. Based on this characterisation, endosperm from the developing grain 8–12 days post-anthesis was chosen for isolating mRNA and preparing cDNA. At this stage in development the mRNA population is not yet dominated by the accumulation of mRNA from seed storage protein genes. A cDNA library, not normalised, containing a high percentage of full length cDNA clones was constructed and 4,319 clones sequenced (\"single-pass\"). Partitioning of the cDNA sequences into gene families and singletons provided the basis for quantifying the accumulation of sequence classes relative to the total number of sequences determined. The accumulation of gene families/singletons was not linear. However, mathematical modeling of the data suggested that the maximum number of different genes expressed is within the range of 4,500–8,000 (detailed in the Appendix). If an average is taken of these extremes, approximately 27% of the gene products were visible as proteins in the 2D-electrophoretic analysis. Analysis of a functional class of genes relevant to wheat grain end-use, namely the glutenin/gliadin seed storage protein class of genes, revealed a new category of gene characterised by a distinctive N-terminal domain and a reduced central repetitive domain. Electronic Publication 相似文献
5.
利用52个家蚕品种在春秋两个季节的试验资料,对万头茧层量及其构成因素作了通径分析。结果表明:不同环境下,诸因素对万头茧层量的作用不完全相同,主要表现为幼虫生命率和茧层率在不同季节中的作用相对地变化。结合育种实践指出:(1)春用蚕品种的选育应在保证生命率的前提下努力提高茧层率和全茧量,而夏秋用品种的选育应在保证茧层率的前提下努力提高生命率和全茧量。 (2)为提高选择效果,春蚕期育种应以选择茧层率为主,夏秋期育种应以选择生命率为主。 相似文献
6.
Camilo L. Quarin 《Sexual plant reproduction》1999,11(6):331-335
It is generally accepted that most angiosperms require an accurate balance between maternal and paternal genome contribution
for endosperm development. The endosperm balance number (EBN) hypothesis postulates that each species has an effective number
which must be in a 2:1 maternal to paternal ratio for normal endosperm development and seed formation. The aim of this work
was to investigate the effect of different sources and ploidy levels of pollen donors on endosperm formation and seed production
of aposporous tetraploid (2n=4×=40) Paspalum notatum. Hand-emasculated spikelets of an apomictic 4× plant were dusted with pollen of 2×, 4×, 5×, 6× and 8× races of the same species;
3× and 4× races of a phylogenetically closely related species, P. cromyorrhizon; and 2× and 4× races of P. simplex, a species of a different subgenus. Experiments including self-pollination as well as emasculation without pollination were
conducted for controls. Results indicated that apomictic 4×P. notatum is a pseudogamous species with effective fertilization of the two unreduced (2n) polar nuclei by a reduced (n) sperm. Endosperm
development and seed production occurred independently of the species or the ploidy level of the pollen donor. However, seed
germination rates were significantly lower than in the self-pollinated control when the pollen donor was 3×P. cromyorrhizon or 2× and 4×P. simplex. Aposporous embryo sacs in Paspalum contribute to endosperm formation with two unreduced (2n) polar nuclei, while the male contribution is the same as in sexual
plants (n). Since sexual Paspalum plants fit the EBN hypothesis, the EBN insensitivity observed in apomictic plants might be a prerequisite for the spread
of pseudogamous apomixis. The EBN insensitivity could have arisen as an imprinting consequence of a high maternal genome contribution.
Received: 20 February 1998 / Revision accepted: 21 October 1998 相似文献
7.
谷类作物胚乳性状遗传控制的鉴别 总被引:30,自引:7,他引:30
谷类作物种子胚乳生状的遗传表达,可能受三倍体的胚乳基因型和/或二倍体的母体基因型控制,还可能存在细胞质效应。Foolad等和Pooni等提出的分析模型,由于遗传参数的系数间存在线性相关,不能有效地区分上述遗传控制系统。本文的交配设计和相应统计方法,可对一胚乳生状是否存在胚乳基因型,母体基因型蔌细腻质效应分别作出测验,从而可确定合适遗传模型和估计有关遗传参数。这些方法也可方便地推广于鉴别非谷作物种子 相似文献
8.
9.
Potokina E Sreenivasulu N Altschmied L Michalek W Graner A 《Functional & integrative genomics》2002,2(1-2):28-39
A barley cDNA macroarray comprising 1,440 unique genes was used to analyze the spatial and temporal patterns of gene expression
in embryo, scutellum and endosperm tissue during different stages of germination. Among the set of expressed genes, 69 displayed
the highest mRNA level in endosperm tissue, 58 were up-regulated in both embryo and scutellum, 11 were specifically expressed
in the embryo and 16 in scutellum tissue. Based on Blast X analyses, 70% of the differentially expressed genes could be assigned
a putative function. One set of genes, expressed in both embryo and scutellum tissue, included functions in cell division,
protein translation, nucleotide metabolism, carbohydrate metabolism and some transporters. The other set of genes expressed
in endosperm encodes several metabolic pathways including carbohydrate and amino acid metabolism as well as protease inhibitors
and storage proteins. As shown for a storage protein and a trypsin inhibitor, the endosperm of the germinating barley grain
contains a considerable amount of residual mRNA which was produced during seed development and which is degraded during early
stages of germination. Based on similar expression patterns in the endosperm tissue, we identified 29 genes which may undergo
the same degradation process.
Electronic Publication 相似文献
10.
棉花组织培养中异常苗的发生与转化 总被引:10,自引:0,他引:10
研究了棉花 (Gossypium hirsutum L.)组织培养中异常苗发生的类型、规律、影响因素及转化为正常苗的途径及技术。结果表明 ,在棉花组织培养中异常苗发生的频率极高 ,且形式多样 ,大体可分为生长点异常苗、叶片异常苗、胚轴异常苗、联体苗、丛生叶苗、单叶苗、玻璃化苗、白化苗、褐化苗和重新愈伤化苗等 1 0类。其中生长点异常苗和叶片异常苗最为常见。影响异常苗形成的因素很多 ,其中主要有外植体种类、培养基组成、培养方式和培养时间。有的异常苗来源于畸形胚 ,有的异常苗由正常苗转化而来。在合适的条件下异常苗可转化为正常苗 ,但不同培养基对异常苗转化为正常苗的影响不同 ,且不同基因型的异常苗转化为正常苗的能力也有差别。此外 ,从外界调控机制与棉花培养细胞的内在发育机制的相互作用方面讨论了造成棉花组织培养异常苗发生的原因 ;并讨论了降低异常苗产生频率的技术途径和异常苗存在对棉花组织培养的影响 相似文献
11.
12.
There was a high frequency in the occurrence of abnormal plantlets during cotton (Gossypium hirsutum L. ) tissue culture. Their patterns, ways of development and effected factors, and the technique of their normalization were studied. Based on their morphologic characters, they could be classified into ten kinds, viz. growing point-abnormal plantlets, cotyledon-, hypocotyl-, united-, fasciculated-, single-leaf-, albino-, vitreous-, browning-, and callus forming plantlets. The growing point- and the cotyledon-abnormal plantlets, which were more commonly seen and were affected by multiple factors, are mainly influenced by the kind of explants, the medium composition, the method and time of culture. The abnormal plantlets could either developed from abnormal embryos or transformed from normal plantlets. Under suitable culture condition reversion of abnormality to normal was possible, however such normalization varied with different genotypes and media. The authors point out the interaction of external regulation and intrinsic developmental mechanism as the main factor causing the accurrence of abnormal plantlet and also discuss the technical procedures of reducing the occurrence frequency of such abnormal plantlets which greatly impact cotton tissue culture. 相似文献
13.
中华猕猴桃胚乳植株后代的观察 总被引:2,自引:0,他引:2
对438株定植的中华猕猴桃胚乳培.养的试管苗,经四年的田间观察,并进行连续二年结果分析。与对照的母株相比,胚乳植株在株形、叶片大小、果实形态及果实的主要营养成分含量上都有较大的变化。同时还发现,由同一块愈伤组织诱导的胚乳试管苗后代中也有雌、雄性别的分化。胚乳植株后代的多样性,可为中华猕猴桃的选种及品种繁育提供丰富的材料。 相似文献
14.
槐种子发育中胚乳细胞半乳甘露聚糖积累的研究 总被引:2,自引:0,他引:2
槐 ( Sophora japonica L.)开花约 60 d至种子成熟 ,为胚乳半乳甘露聚糖积累期。用组织化学方法 ,对储藏于胚乳细胞壁上的半乳甘露聚糖的形成积累进行了观察 ,结果表明 ,半乳甘露聚糖最先在邻近胚的胚乳细胞的粗面内质网的囊泡腔内形成 ,并通过细胞质膜分泌至细胞壁周围。此后 ,半乳甘露聚糖的积累逐渐向种皮方向扩展 ,及至种子成熟时 ,除糊粉层外 ,所有胚乳细胞几乎全由多糖所填充。此外 ,对半乳甘露聚糖发生部位及其积累过程的消长变化进行了讨论 相似文献
15.
芍药胚和胚乳早期发育的研究 总被引:3,自引:0,他引:3
本文报道芍药(Paeonia lactiflora)的胚和胚乳的早期发育,主要结论是:1,开花后4—20天,合子核反复分裂形成多核原胚。2.原胚及胚乳游离核分裂均以有丝分裂为主,晚期有无丝分裂和多倍体核;3,细胞壁形成可由纺锤丝间和自由壁两种方式进行。原胚壁形成由合点端向珠孔端进行,胚乳则由胚附近向合点端发展。我们支持 Cave 等基于多核原胚提出的 Paeonia 与裸子植物平行演化的意见,同时认为 Paeonia 的多核原胚演化趋势是原胚由珠孔端至合点端功能分区的特化。 相似文献
16.
Maria J. Carmona C. Hernández-Lucas Carmen San Martin P. González F. García-Olmedo 《Protoplasma》1993,173(1-2):1-7
Summary Thionins are cysteine-rich polypeptides of about 5,000 Da. Localization at the subcellular level of type I endosperm thionins has been carried out by immunogold labeling, using an antibody that recognizes type I thionin variants. In developing wheat and barley caryopses, sectioned at different times between 13 and 24 days after flowering, this type of thionins was only detected around protein bodies from cells of the starchy endosperm, using light microscopy. Electron microscopy revealed that these proteins were located in electron-dense spheroids in the periphery of protein bodies, at the earlier stages, whereas later the label appeared also as a thin layer around these organelles.Abbreviations DAF
days after flowering
- RER
rough endoplasmic reticulum 相似文献
17.
以盾叶薯蓣(Dioscorea zingiberensis)的胚乳为外植体,研究了不同植物生长调节剂对胚乳愈伤组织诱导及植株再生的影响,并鉴定了再生植株。结果表明:愈伤组织诱导形成的适宜培养基为MS+2.0mg·L^–12,4-D+0.5mg·L^–16-BA,不定芽分化的适宜培养基为MS+2.0mg·L^–16-BA+0.1mg·L^–1NAA,生根的适宜培养基为1/2MS+0.3mg·L^–1NAA;再生植株炼苗移栽后,成活率可达80%;对获得的再生植株腋芽生长点进行染色体制片观察,发现染色体数目为20的细胞占观察细胞总数的10%,染色体数目为21–29的细胞占16%,染色体数为30的细胞占74%;获得了三倍体植株。 相似文献
18.
The present paper reports the early development of embryo and endosperm of Paeonia lactiflora. The main conclusions are as follows: 1 The zygote nucleus divides directly to form a coenocytic proembryo with different number of free nuclei. The result confirms the conclusion of Yakovlev[6] as well as Yakovlev and Yoffe[7] On the occurnce of coenocytic proembryo in Paeonia suffruticosa Andr. (P. moutan Sims), P. albiflora Pall. (P. lactiflora Pall), P. officinalis L., P. tenuifolia L., P. anomala L., P. veitchii Lynch (P. beresowskii Komarov), P. wittmanniana, also it agrees with the report of Cave et al.[4] on the occurence of the coenocytie proembryo in Paeonia californica and P. brownii. From the result of our investigation, there is no basis to support Murgai's conclusion obtained in certain species of Paeonia, i.e., the first division of zygote nucleus is accompanied by wall formation and the coenocyte is a suspensor. The primary endosperm nucleus of P. lactiflora divides often earlier than zygote nucleus, or almost at the same time or later in a few cases; 2 Both mitosis and amitosis occur in the free nuclei in the coenocytic proembryo, and mitosis is dominant. In the later stage of development the amitosis occurs at the micropylar region of the coenocytic proembryo, in the free nuclear endosperm at the chalazal region and the appressed part of the chalazal end of the coenocytic proembryo. In addition, in the region of conenocytic proembryo and endosperm polyploid nuclei, irregular nuclei are also frequently met with; 3 Cell wall formation in the coenocyte and the endosperm initiates by means of both cell plate and freely growthing walls, but in the coenocyte wall formation is earlier than in the free nuclear endosperm. At first, wall formation of the coenocytic proembryo begins at the chalazal end, and then extends toward the micropylar region, and in endosperm it begins at the part appressed to the part of the chalazal end of coenocytic proembryo, and then extends toward the chalazal end. We support Cave’s suggestion of the parallel evolution for Paeonia possessed the coenocytic proembryo has no relation to the coenocytic proembryo of the gymnosperms. Further we consider the evolution tendency of the coenocytic proembryo of Paeonia toward a functional specialization. 相似文献
19.
本文运用石蜡切片法、整体透明法研究了草地早熟禾的假受精现象。结果表明,草地早熟禾在两极核清晰可见时,卵细胞就已自发分裂成原胚,此现象占观察总数88%;但是,其极核必需经过受精过程才能发育为胚乳。 相似文献
20.
The extraction of RNA from a starchy plant material, such as many common food grains, is difficult, and especially so from the mature endosperm of rice. Most commercial RNA kits are not suitable for starchy materials. Traditional RNA extraction procedures, in addition to being laborious and time consuming, leave hazardous organic wastes that result in expensive disposal costs. Interestingly, the numerous commercial DNA isolation kits now available often include directions for eliminating co-isolated RNA. This indicated an approach to obtain the generally unwanted RNA by-product by treating the total extraction product to intentionally retain RNA. A method was developed by which a two-step DNase procedure was applied to the product of the Cartagen Food DNA extraction kit that eliminated the DNA but left the co-extracted RNA. This modified procedure was compared with several other commercial and standard methods that are promoted as being able to work under high polysaccharide conditions. Successful extraction was determined by the production and amplification of cDNA by RT-PCR of actin. Extraction was successful from milled rice, as well as from cornmeal and wheat flour. The modification provides an RNA extraction method that is quick, easy, and inexpensive, and also eliminates the production of hazardous wastes. 相似文献