Isozyme Variation in Wild and Cultivated Species of the Genus Trifolium L. (Leguminosae)

Isozyme patterns for PGI (phosphoglucoisomerase), MDH (malatedehydrogenase), EST (esterase) and SOD (superoxide dismutase)were evaluated in 36 accessions of eight Trifolium species,namely T. incarnatum, T. polymorphum, T. pratense, T. repens,T. resupinatum, T. riograndense, T. subterraneum and T. vesiculosum.Similarity between species and accessions was estimated by Jaccard’ssimilarity index based on presence or absence of bands. TheUPGMA method was utilized for the groupings and dendrogram constructionwith the aid of the NTSYS-PC program. Interspecific similaritywas low (J 0.351). The dendrogram presented eight groups, eachone corresponding to a taxonomic species. Most of the accessionsof the same species grouped together at J > 0.50, exceptT. riograndense, T. repens and T. pratense. These three speciesshowed the lowest similarity between their accessions, reflectinghigher intraspecific variation. Some accession-specific bandswere identified. The species groupings are consistent with traditionaltaxonomic species delimitation. Therefore isozyme patterns,especially when several systems are employed, are useful andreliable biochemical markers for the taxonomic delimitationand characterization of Trifolium germplasm. Copyright 2000Annals of Botany Company Genetic diversity, germplasm characterization, isoenzymatic variability, biochemical markers, isozymes,Trifolium     

Role of Bcl-2 Family Members in Anoxia Induced Cell Death

Anoxia, the condition of oxygen deprivation, induces apoptosis via the intrinsic apoptoticpathway. Cells deficient in both Bax and Bak do not undergo cell death during anoxia.However, the underlying mechanism of anoxia induced cell death is not well defined. Herewe report our latest findings of two critical events that are required to induce cell deathduring anoxia. First, a key member of the Bcl-2 family of pro-survival proteins, Mcl-1,undergoes proteasomal-dependent degradation. The loss of Mcl-1 protein is independentof Bax or Bak indicating this is an early event in the apoptotic cascade. Second, cellsinhibit the mitochondrial electron transport chain to negate the pro-survival function of Bcl-2/Bcl-XL. These observations indicate that loss of pro-survival function is necessary foranoxia induced cell death.     

Comparison of Embryo Development in Wild and Cultivated Arachis Species

Embryo development following selfing was investigated in twowild diploid peanut species, Arachis batizocoi Krap. et Greg.(coll. K 9484) (2n = 20) and A. duranensis Krap. et Greg. nom.nud. (coll. K 7988) (2n = 20), and one cultivated tetraploidspecies, A. hypogaea L. NC-Ac 18000 (2n = 40). Rates of pegelongation and sequences of embryo development for each specieswere compared. Peg elongation rates were similar for the twowild species, but for A. hypogaea it was only one-third to one-halfthat of the diploid species. Embryos in A. hypogaea showed slightlymore rapid cell division than in the wild species. The observedvariation in reproductive development between the wild and cultivatedspecies indicate that different control mechanisms may governdevelopment in the different species and may be at least partiallyresponsible for failure to produce viable interspecific hybridsat various ploidy levels. The observations are also importantfor determining the time at which embryos of different speciesof Arachis will reach the appropriate stage of development forsuccessful culture on an artificial medium during embryo rescueprocedures. Peanut, Arachis hypogaea, wild species, embryo, peg     

Chlorophyll Content in Some Cultivated and Wild Species of the Family Lamiaceae

Chlorophyll (Chl) a, b and (a+b) contents were measured in eleven cultivated and wild species of Lamiaceae collected from different environments. In nine of these eleven species, belonging to the subfamily Nepetoidea, the Chl a/b ratio was low. This suggests a prevailing shade aspect, regardless of collection sites and cultivated or wild origin.     

Mitochondrial Genome Analysis of Wild Rice (Oryza minuta) and Its Comparison with Other Related Species

Oryza minuta (Poaceae family) is a tetraploid wild relative of cultivated rice with a BBCC genome. O. minuta has the potential to resist against various pathogenic diseases such as bacterial blight (BB), white backed planthopper (WBPH) and brown plant hopper (BPH). Here, we sequenced and annotated the complete mitochondrial genome of O. minuta. The mtDNA genome is 515,022 bp, containing 60 protein coding genes, 31 tRNA genes and two rRNA genes. The mitochondrial genome organization and the gene content at the nucleotide level are highly similar (89%) to that of O. rufipogon. Comparison with other related species revealed that most of the genes with known function are conserved among the Poaceae members. Similarly, O. minuta mt genome shared 24 protein-coding genes, 15 tRNA genes and 1 ribosomal RNA gene with other rice species (indica and japonica). The evolutionary relationship and phylogenetic analysis revealed that O. minuta is more closely related to O. rufipogon than to any other related species. Such studies are essential to understand the evolutionary divergence among species and analyze common gene pools to combat risks in the current scenario of a changing environment.     

棉属栽培种与野生种杂交的不亲和性

本文研究了棉属栽培种与野生种杂交的不亲和性,试验材料涉及5个染色体组,包括2个栽培种(陆地棉和中棉)和5个野生种(戴维逊氏棉、瑟伯氏棉、三裂棉、阿拉伯棉和比克氏棉)。以陆地棉作母本,异己花粉管在花柱中生长缓慢,有花粉管胚珠低于10%,陆地棉×戴维逊氏棉杂种胚在子叶期坏死。以中棉作母本,不亲和性主要表现在受精后的胚胎发育过程中。     

Studies of Karyotypes in Three Wild and Four Cultivated Species of Gossypium

Karyotypes in seven species of Gossypium, G. thurberi, G. advidsonii, G. raimondii of D group; G. herbaceum, G. arboreum of A group; G. hirsutum and G. ba- rbadense of AD group were studied in 1983. It can be simplified as follows: G. thurberi 2n = 2x = 26 = 24m + 2Sm (2SAT); G. davidsonii 2n= 2x = 26 20m+6Sm(4SAT); G. raimondii 2n=2x= 26= 20m+6Sm(2SAT); G. herbaceum 2n = 2x = 26 = 18m + 4Sm+4St(4SAT); G. arboreum 2n = 2x = 26 = 18m + 6Sm (2SAT) + 2St(2SAT); G. hirsutum 2n = 4x =52 = 32m + 18Sm(4SAT) +2St (2 SAT); G. barbadense 2n = 4x = 52 = 38m + 12Sm (2SAT) + 2St(2SAT). This paper also deals with the supplier in A group and D group of tetraploids.     

Distribution of Brown Blotch Bacteria in Wild and Cultivated Species of Basidiomycetes

Wild and cultivated Basidiomycetes species were cultured to determine the distribution of bacteria causing brown blotch disease of Agaricus bisporus. Colonies from each basidiocarp were screened for brown blotch organisms by the white line and host pathogenicity tests. Isolates causing brown blotch were identified as Pseudomonas tolaasi and an Arthrobacter species.     

Bcl-2 Family Members and Functional Electron Transport Chain Regulate Oxygen Deprivation-Induced Cell Death

The mechanisms underlying cell death during oxygen deprivation are unknown. We report here a model for oxygen deprivation-induced apoptosis. The death observed during oxygen deprivation involves a decrease in the mitochondrial membrane potential, followed by the release of cytochrome c and the activation of caspase-9. Bcl-X(L) prevented oxygen deprivation-induced cell death by inhibiting the release of cytochrome c and caspase-9 activation. The ability of Bcl-X(L) to prevent cell death was dependent on allowing the import of glycolytic ATP into the mitochondria to generate an inner mitochondrial membrane potential through the F(1)F(0)-ATP synthase. In contrast, although activated Akt has been shown to inhibit apoptosis induced by a variety of apoptotic stimuli, it did not prevent cell death during oxygen deprivation. In addition to Bcl-X(L), cells devoid of mitochondrial DNA (rho degrees cells) that lack a functional electron transport chain were resistant to oxygen deprivation. Further, murine embryonic fibroblasts from bax(-/-) bak(-/-) mice did not die in response to oxygen deprivation. These data suggest that when subjected to oxygen deprivation, cells die as a result of an inability to maintain a mitochondrial membrane potential through the import of glycolytic ATP. Proapoptotic Bcl-2 family members and a functional electron transport chain are required to initiate cell death in response to oxygen deprivation.     

Hedgehogs as Negative Regulators of the Cell Cycle

During the development of multicellular animals, cell proliferation must be precisely controlled, as deregulated proliferation can lead to overgrowth and cancer. In addition, proliferation must be tightly integrated with pattern formation and differentiation to generate the required number of cells in the right organs, and at the right time. All major signaling pathways employed during embryogenesis have been implicated in cell cycle regulation, indicating that no single pathway has been dedicated to this task. Also, the precise role of a particular signaling pathway in regulating proliferation is highly dependent on the cellular context, and may have opposite effects on cell-cycle progression in different cells and tissues. The Hedgehog (Hh) family of signaling proteins is known to control both differentiation and proliferation during development. So far, studies addressing the effect of Hh signaling on proliferation have shown it to have a stimulatory effect on cell-cycle progression. Here we review several recent studies indicating that Hh signaling can also have the opposite effect, directing cell-cycle exit in a number of cell types in vertebrate and in invertebrate embryos.     

动物细胞培养过程中的细胞凋亡

细胞培养过程中的细胞凋亡是细胞受环境因素的影响而发生的现象。随着对细胞凋亡的分子生物学和细胞生物学了解的深入,显示了有效地控制动物细胞培养中细胞凋亡的巨大潜力。包括采用ＤＮＡ重组技术把抗细胞凋亡的基因导入细胞和在培基中加入具有抗细胞凋亡的生存因子或化合物等手段已用于控制细胞培养过程中的细胞凋亡。这些技术将大大延长细胞达到饱和密度后的培养时间,提高细胞培养系统的生产效率。     

Morphogenetic Potential of Cultured Leaf Sections of Cultivated and Wild Species of Tomato

Leaf explants of the cultivated tomato Lycopersicon esculentumcv. Rheinlands Rhum (RR) and the mutant flacca (flc), and thetwo wild species L. peruvianum (Lp) and Solanum pennellii (Sp)accession Atico were cultured on a modified Murashige and Skoog'smedium with various combinations of either kinetin (KN)+indol-3y1acetic acid (LAA), Kn⁺ naphthalene acetic acid or benzyladenine+IAA. The wild species Lp, was found to have the highest morphogeneticpotential as expressed by root and shoot formation in the variousmedia, as compared with the other species. The morphogeneticresponse of the second wild species, Sp varied in the differentmedia, being the poorest in the medium containing KN+LAA andbetter in the other media. The response of flc mutant, whichis distinguished by its hormonal imbalance, was not appreciablydifferent from that of the control normal plant, RR.     

Comparative Embryo Sac Morphology at Anthesis of Cultivated and Wild Species of Arachis

Introgression of germplasm from wild to cultivated species ofArachis is severely impeded because abortion processes oftenoccur as a prepeg-, peg-(gynophore), or postpeg-elongation event.A comparative study of embryo sac morphology at anthesis wasundertaken to determine if observable differences were presentthat could possibly explain abortion prior to peg tip swellingfollowing soil penetration. Two wild Arachis species (A. duranensisand A. stenosperma) plus A. hypogaea cultivars NC 6 and Argentinewere studied. Differences in starch grain concentration andcytoplasmic stranding organization were observed between A.hypogaea cultivars and the wild Arachis species. These differencesprobably have a significant impact on energy availability atsyngamy and the subsequent early cell division of the embryo.An improper energy balance could contribute to the onset ofabortion in interspecific hybrids. Modification in egg apparatusorganization among all species was also observed which may accountfor low percentages of seed recovery resulting from interspecifichybridization attempts. Embryo sac morphology, interspecific hybridization, Arachis hypogaea L., Arachis species, light microscopy, scanning electron microscopy, embryo abortion, fertilization incompatibility, peanuts, groundnut     

RAPD鉴定栽培稻与野生稻体细胞杂种

利用随机引物扩增DNA(RAPD)技术,对栽培稻和野生稻原生质体融合获得的体 细胞杂种进行了鉴定。证实了它们包含有双亲的基因组成分。但来自双亲的基因组成分并不是对等的。一些体细胞杂种含有一个亲本更多的基因组成分,而另一些相反。利用RAPD数据和聚类图讨论了体细胞杂种和双亲的亲缘关系。     

厚朴野生种与栽培种花不同部位香气成分分析

以厚朴野生种和栽培种苞片刚裂开的花苞为试材,采用固相微萃取和气相色谱—质谱(GC/MS)分析技术对其进行香气成分和相对含量的测定,比较分析了花朵不同部位香气成分的差异。结果表明：厚朴野生种共有39种香气成分,雌雄蕊中26种,花瓣中22种,栽培种中75种香气成分,雌雄蕊中49种,花瓣中54种。萜烯类是两种厚朴花苞中最重要的香气化合物,莰烯、罗勒烯异构体混合物、石竹烯、芳樟醇是野生种和栽培种中共有的相对含量较高的香气成分。厚朴野生种和栽培种间以及同种厚朴雌雄蕊与花瓣之间的香气成分的种类和相对含量差异显著。     

Inhibition of Mitochondrial Neural Cell Death Pathways by Protein Transduction of Bcl-2 Family Proteins

Bcl-2 and other closely related members of the Bcl-2 family of proteins inhibit the death of neurons and many other cells in response to a wide variety of pathogenic stimuli. Bcl-2 inhibition of apoptosis is mediated by its binding to pro-apoptotic proteins, e.g., Bax and tBid, inhibition of their oligomerization, and thus inhibition of mitochondrial outer membrane pore formation, through which other pro-apoptotic proteins, e.g., cytochrome c, are released to the cytosol. Bcl-2 also exhibits an indirect antioxidant activity caused by a sub-toxic elevation of mitochondrial production of reactive oxygen species and a compensatory increase in expression of antioxidant gene products. While classic approaches to cytoprotection based on Bcl-2 family gene delivery have significant limitations, cellular protein transduction represents a new and exciting approach utilizing peptides and proteins as drugs with intracellular targets. The mechanism by which proteins with transduction domains are taken up by cells and delivered to their targets is controversial but usually involves endocytosis. The effectiveness of transduced proteins may therefore be limited by their release from endosomes into the cytosol.     

The Functional Differences between Pro-survival and Pro-apoptotic B Cell Lymphoma 2 (Bcl-2) Proteins Depend on Structural Differences in Their Bcl-2 Homology 3 (BH3) Domains

Bcl-2 homology 3 (BH3) domains are short sequence motifs that mediate nearly all protein-protein interactions between B cell lymphoma 2 (Bcl-2) family proteins in the intrinsic apoptotic cell death pathway. These sequences are found on both pro-survival and pro-apoptotic members, although their primary function is believed to be associated with induction of cell death. Here, we identify critical features of the BH3 domains of pro-survival proteins that distinguish them functionally from their pro-apoptotic counterparts. Biochemical and x-ray crystallographic studies demonstrate that these differences reduce the capacity of most pro-survival proteins to form high affinity “BH3-in-groove” complexes that are critical for cell death induction. Switching these residues for the corresponding residues in Bcl-2 homologous antagonist/killer (Bak) increases the binding affinity of isolated BH3 domains for pro-survival proteins; however, their exchange in the context of the parental protein causes rapid proteasomal degradation due to protein destabilization. This is supported by further x-ray crystallographic studies that capture elements of this destabilization in one pro-survival protein, Bcl-w. In pro-apoptotic Bak, we demonstrate that the corresponding distinguishing residues are important for its cell-killing capacity and antagonism by pro-survival proteins.