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1.
Variation in the ability to form ectomycorrhizas in the F1 progeny of an interspecific poplar (Populus spp.) cross 总被引:2,自引:0,他引:2
D. Tagu Patricia Faivre Rampant Frédéric Lapeyrie Pascale Frey-Klett Patrice Vion Marc Villar 《Mycorrhiza》2001,10(5):237-240
The aim of this study was to determine the existence of a genetic basis for the ability to form ectomycorrhiza on a model
angiosperm tree (Populus, poplar). Parental clones and 18 progeny from a controlled interspecific cross between Populus deltoides and Po- pulus trichocarpa were grown in a glasshouse and inoculated with mycelium of the ectomycorrhizal fungus Laccaria bicolor. Three months after inoculation, the percentage of mycorrhizal root tips was determined for each inoculated plant. The data
indicate variability in the ability to form ectomycorrhizas among the F1 progeny, including individual progeny which are different
to either parent. This suggests a genetic basis for mycorrhiza formation.
Accepted: 6 November 2000 相似文献
2.
Involvement of putrescine in the inductive rooting phase of poplar shoots raised in vitro 总被引:1,自引:0,他引:1
Micropropagated poplar shoots rooted 100% on a rooting medium (A) containing NAA, but they did not root in the absence of auxin (NA). Putrescine, but not spermidine and spermine, promoted rooting up to 42% when added to the NA medium. Cyclohexylamine (CHA), an inhibitor of spermine synthase, also promoted (up to 36%) rooting in the absence of auxin. The inhibitors of polyamine biosynthesis DFMA (α-difluoromethylarginine) and DFMO (α-difluoromethylomithine), aminoguanidine (AG) and methylglyoxal-bis-guanylhydrazone (MGBG), inhibited rooting when applied in the presence of auxin and had no effect in its absence.
The rooting inductive phase (in the presence of auxin) was determined by periodical transfer of shoots from A to NA medium, and by changes in peroxidase activity, to be 7 h. Putrescine (not spermidine and spermine) accumulated to a maximum during the inductive phase. Both putrescine and CHA promoted rooting on NA medium when applied during the first 7 h. In contrast DFMA and AG inhibited rooting during this period. The results point to the involvement of putrescine and its Δ1 -pyrroline pathway, in the inductive phase of rooting in poplar shoots. 相似文献
The rooting inductive phase (in the presence of auxin) was determined by periodical transfer of shoots from A to NA medium, and by changes in peroxidase activity, to be 7 h. Putrescine (not spermidine and spermine) accumulated to a maximum during the inductive phase. Both putrescine and CHA promoted rooting on NA medium when applied during the first 7 h. In contrast DFMA and AG inhibited rooting during this period. The results point to the involvement of putrescine and its Δ
3.
Dicot wood is mainly composed of cellulose, lignin and glucuronoxylan (GX). Although the biosynthetic genes for cellulose and lignin have been studied intensively, little is known about the genes involved in the biosynthesis of GX during wood formation. Here, we report the molecular characterization of two genes, PoGT8D and PoGT43B, which encode putative glycosyltransferases, in the hybrid poplar Populus alba x tremula. The predicted amino acid sequences of PoGT8D and PoGT43B exhibit 89 and 75% similarity to the Arabidopsis thaliana IRREGULAR XYLEM8 (IRX8) and IRX9, respectively, both of which have been shown to be required for GX biosynthesis. The PoGT8D and PoGT43B genes were found to be expressed in cells undergoing secondary wall thickening, including the primary xylem, secondary xylem and phloem fibers in stems, and the secondary xylem in roots. Both PoGT8D and PoGT43B are predicted to be type II membrane proteins and shown to be targeted to Golgi. Overexpression of PoGT43B in the irx9 mutant was able to rescue the defects in plant size and secondary wall thickness and partially restore the xylose content. Taken together, our results demonstrate that PoGT8D and PoGT43B are Golgi-localized, secondary wall-associated proteins, and PoGT43B is a functional ortholog of IRX9 involved in GX biosynthesis during wood formation. 相似文献
4.
Kocsy G von Ballmoos P Suter M Rüegsegger A Galli U Szalai G Galiba G Brunold C 《Planta》2000,211(4):528-536
The role of glutathione (GSH) in protecting plants from chilling injury was analyzed in seedlings of a chilling-tolerant
maize (Zea mays L.) genotype using buthionine sulfoximine (BSO), a specific inhibitor of γ-glutamylcysteine (γEC) synthetase, the first enzyme
of GSH synthesis. At 25 °C, 1 mM BSO significantly increased cysteine and reduced GSH content and GSH reductase (GR: EC 1.6.4.2)
activity, but interestingly affected neither fresh weight nor dry weight nor relative injury. Application of BSO up to 1 mM
during chilling at 5 °C reduced the fresh and dry weights of shoots and roots and increased relative injury from 10 to almost
40%. Buthionine sulfoximine also induced a decrease in GR activity of 90 and 40% in roots and shoots, respectively. Addition
of GSH or γEC together with BSO to the nutrient solution protected the seedlings from the BSO effect by increasing the levels
of GSH and GR activity in roots and shoots. During chilling, the level of abscisic acid increased both in controls and BSO-treated
seedlings and decreased after chilling in roots and shoots of the controls and in the roots of BSO-treated seedlings, but
increased in their shoots. Taken together, our results show that BSO did not reduce chilling tolerance of the maize genotype
analyzed by inhibiting abscisic acid accumulation but by establishing a low level of GSH, which also induced a decrease in
GR activity.
Received: 9 November 1999 / Accepted: 17 February 2000 相似文献
5.
R. L. Wu 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1997,94(1):104-114
Understanding the genetic mechanisms for the phenotypic plasticity and developmental instability of a quantitative trait
has important implications for breeding and evolution. Two clonally replicated plantations of two 3-generation inbred pedigrees
derived from the highly divergent species Populus trichocarpa and P. deltoides were used to examine the genetic control of macro- and micro-environmental sensitivities and their genetic relationships
with the trait mean across two contrasting environments. For all stem-growth traits studied, the trait mean had a higher broad-sense
heritability (H2) level than macroenvironmental sensitivity, both with much higher values than microenvironmental sensitivity. Genetic correlation analyses indicated that the trait mean was more or less independent
of macro- or micro-environmental sensitivity in stem height. Thus, for this trait, the genetic difference in response to the
two environments might be mainly due to epistasis between some regulatory loci for plasticity and loci for trait mean. However,
for basal area and volume index, pleiotropic loci might be more important for their genetic differences between the two environments.
No evidence was found to support Lerner’s (1954) homeostasis theory in which macro- or micro-environmental sensitivity is
the inverse function of heterozygosity.
Received: 8 March 1996 / Accepted: 31 May 1996 相似文献
6.
The chilling injury induced by high root temperature in the leaves of rice seedlings 总被引:2,自引:0,他引:2
Root temperature is found to be a very important factor forleaves to alter the response and susceptibility to chillingstress. Severe visible damage was observed in the most activeleaves of seedlings of a japonica rice (Oryza sativa cv. Akitakomachi),e.g. the third leaf at the third-leaf stage, after the treatmentwhere only leaves but not roots were chilled (L/H). On the otherhand, no visible damage was observed after the treatment whereboth leaves and roots were chilled simultaneously (L/L). Thechilling injury induced by L/H, a novel type of chilling injury,required the light either during or after the chilling in orderto develop the visible symptoms such as leaf bleaching and tissuenecrosis. Chlorophyll fluorescence parameters measured aftervarious lengths of chilling treatments showed that significantchanges were induced before the visible injury. The effectivequantum yield and photochemical quenching of PSII dropped dramaticallywithin 24 h in both the presence and absence of a 12 h lightperiod. The maximal quantum yield and non-photochemical quenchingof PSII decreased significantly only in the presence of light.On the other hand, L/H chilling did not affect the functionof PSI, but caused a significant decrease in the electron availabilityfor PSI. These results suggest that the leaf chilling with highroot temperature destroys some component between PSII and PSIwithout the aid of light, which causes the over-reduction ofPSII in the light, and thereby the visible injury is inducedonly in the light. 相似文献
7.
Wood formation in poplar: identification, characterization, and seasonal variation of xylem proteins 总被引:9,自引:0,他引:9
Proteins that are preferentially produced in developing xylem may play a substantial role in xylogenesis. To reveal the identity
of these proteins, comparative two-dimensional polyacrylamide gel electrophoresis was performed on young differentiating xylem,
mature xylem, and bark of poplar (Populus trichocarpa Hook. cv. `Trichobel') harvested at different times of the year. The most-abundant xylem proteins were identified by microsequence
analysis. For 17 of these proteins a putative function could be assigned based on similarity with previously characterized
proteins, and for 15 out of these corresponding expressed sequence tags (ESTs) were found in the poplar EST database. The
identified xylem–preferential proteins, defined by comparing the protein patterns from xylem and bark, were all involved in
the phenylpropanoid pathway: two caffeoyl-coenzyme A O-methyltransferases (CCoAOMT), one phenylcoumaran benzylic ether reductase (PCBER), one bispecific caffeic acid/5-hydroxyferulic
acid O-methyltransferase (COMT), five S-adenosyl-L-methionine synthetases, and one homologue of glycine hydroxymethyltransferase (GHMT). Remarkably, the biological function
of the two most-abundant xylem-preferential proteins (PCBER and a GHMT homologue) remains unclear. In addition, several housekeeping
enzymes were identified: two enolases, two glutamine synthetases, one 70-kDa heat-shock cognate, one calreticulin, and one
α-tubulin. In comparison to the xylem-preferential proteins, the housekeeping proteins were expressed at significant levels
in the bark as well. Also, several additional protein spots were detected for CCoAOMT, PCBER, and COMT by immunoblot. Our
data show that for the study of xylogenesis, two-dimensional protein gel comparisons combined with systematic protein sequencing
may yield information complementary to that from EST sequencing strategies.
Received: 28 June 1999 / Accepted: 3 September 1999 相似文献
8.
R. Van den Driessche 《Plant and Soil》1983,71(1-3):495-499
Summary Four clones of Sitka spruce (Picea sitchensis (Bong.) Carr.) were established from cuttings of two and four-year old material in 1968. Within each clone half the trees were randomly hedged at 1 m in 1977. Cuttings from hedges rooted more freely than cuttings from the lower crown which, in turn, rooted more readily than upper crown cuttings. Rooting occurred most readily during January and early February. Concentrations of sugars in stems and foliage showed little correlation with rooting.Chilling must be completed for most rapid rooting of dormant Sitka spruce cuttings and this requirement can be satisfied by 10 weeks at 2°C. 相似文献
9.
Zeng-hui Hu Ying-bai Shen You-qing Luo Fan-yi Shen Hai-bo Gao Rong-fu Gao 《Journal of Plant Biology》2008,51(4):269-275
Plant aldehydes are volatiles necessary to defenses against environmental stress. To explore their emissions in response to
wounding, we performed gas chromatography-mass spectrometry (GC-MS) on cuttings from poplar (Populus simonii×P. pyramidalis ‘Opera 8277’) that were mechanically damaged to mimic herbivore attack. We detected 16 aldehydes, including 11 linear saturated
aldehydes, 3 linear unsaturated aldehydes, and 2 non-linear aldehydes. Emissions of these aldehydes were clearly enhanced
by such treatment, and exhibited a similar pattern of change, i.e., increasing in the first 2 h, then sharply decreasing before
rising again at about 12 h. Two release peaks for these aldehydes were observed. Therefore, we propose two pathways for the
mediation of aldehyde emissions following damage. The first peak may represent emissions from plant storage pools, whereas
the second release peak might result from greater formationde novo through an activated synthesis pathway. 相似文献
10.
Cell division and cell differentiation are key processes in shoot development. The Arabidopsis thaliana (L.) Heynh. SCHIZOID (SHZ) gene appears to influence cell differentiation and cell division in the shoot. The shz-2 mutant is notable in that distinct phenotypes develop, depending on the environment in which the plants are grown. When shz-2 mutants are grown in petri dishes, callus develops from the petiole and hypocotyl. In contrast, when the mutants are grown
on soil, shoots appear externally stunted with malformed leaves. However, detailed examination of soil-grown mutants shows
that the two phenotypes are related. Soil-grown mutants form adventitious meristems, produce a large amount of vascular tissues
and have aberrant cell divisions in the meristem. Cells with abnormal cell-division patterns were found in the apical and
vascular meristems, suggesting SHZ influences cell division. Development of callus in petri dishes, development of adventitious meristems and aberrations in
leaves on soil suggest that SHZ influences cell differentiation. The distinct, but related phenotypes on soil and in petri dishes suggests that SHZ normally functions to regulate differentiation and/or cell division in a manner that is responsive to environmental conditions.
Received: 30 July 1999 / Accepted: 22 September 1999 相似文献
11.
J. F. Hausman 《Plant Growth Regulation》1993,13(3):263-268
Shoots of poplar (Populus tremula × P. tremuloïdes) were multiplied in vitro and rooted on a rooting medium in the presence of NAA. No rooting occurred in the absence of exogenous auxin. A peak of soluble peroxidase activity, which corresponded to a decrease in the free IAA level in the shoots, preceded rooting These events were considered as corresponding to the initiative phase of rooting. They are preceded by a peak in free IAA activity which might initiate the inductive phase of the rooting process. A burst of ethylene production was measured in both rooting and non-rooting shoots, but the ethylene peak from rooting shoots appeared earlier and was higher. The use of ACC indicated that the exogenous auxin might have enhanced ACC-synthetase activity.Abbreviations ACC
1-aminocyclopropane-1-carboxylic acid
- NAA
naphthaleneacetic acid
- IAA
indole-3-acetic acid
- 2-iP
2-isopentenyladenine
- IAAsp
indole-3-acetylaspartic acid
- IBA
indole-3-butyric acid
- GC
gas-chromatography 相似文献
12.
13.
Development and characterization of microsatellite markers in black poplar (Populus nigra L.) 总被引:6,自引:0,他引:6
J. van der Schoot M. Pospíšková B. Vosman M. J. M. Smulders 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2000,101(1-2):317-322
Using an enrichment procedure, we have cloned and sequenced microsatellite loci from black poplar (Populus nigra L.) and developed primers for sequence-tagged microsatellite (STMS) analysis. Twelve primer pairs for dinucleotide repeats
produced fragments of sufficient quality which were polymorphic in P. nigra. Some of them also showed amplification in other Populus species (P. deltoides, P. tricocarpa, P. tremula, P. tremuloides, P. candicans, and/or P. lasiocarpa). The best nine and (GT) (GA) microsatellite markers were tested on a set of 23 P. nigra genotypes from all over Europe. The microsatellites were highly polymorphic, with 10–19 different alleles per microsatellite
locus among these 23 genotypes. WPMS08 sometimes amplified three fragments. Using the other eight marker loci, the level of
heterozygosity among the plants was on average 0.71 (range 0.25–1.00). The microsatellite markers developed will be useful
for screening the genetic diversity in natural populations and in gene bank collections.
Received: 21 October 1999 / Accepted: 24 November 1999 相似文献
14.
Genes in the FLOWERING LOCUS T (FT) and TERMINAL FLOWER 1 (TFL1)family have been shown to be important in the control of theswitch between vegetative and reproductive growth in severalplant species. We isolated nine members of the FT/TFL1 familyfrom Lombardy poplar (Populus nigra var. italica Koehne). Sequenceanalysis of the members of the FT/TFL1 family revealed considerablehomology within their coding regions both among family membersand to the members of the same family in Arabidopsis, tomatoand grapevine. Moreover, members of this family in all fourspecies examined display a common exon–intron organization.Phylogenetic analysis revealed that the genes fall into fourdifferent clades: two into the TFL1 clade; five into the FTclade; and one each into the MOTHER OF FT AND TFL1 and BROTHEROF FT AND TFL1 clades. One gene in the TFL1 clade, PnTFL1, isexpressed in vegetative meristems, and transgenic Arabidopsisthat ectopically expressed PnTFL1 had a late-flowering phenotype.The expression patterns of two genes in the FT clade, PnFT1and PnFT2, suggested a role for them in the promotion of flowering,and transgenic Arabidopsis that ectopically expressed eitherPnFT1 or PnFT2 had an early-flowering phenotype. 相似文献
15.
The influence of culture chamber capacity, medium volume and culture density on the growth yields of lettuce (Lactuca sativa L.) and spearmint (Mentha spicata L.) shoots were determined in an environment containing either 350 or 10,000 μmol mol–1 CO2 after 8 weeks of incubation. High positive correlations occurred between the culture vessel capacity and spearmint fresh
weight, leaf number, root number, and shoot number. Similarly, high positive correlations occurred between culture vessel
capacity and lettuce fresh weight, leaf number, and root number. Higher fresh weights, leaf numbers, and root numbers were
obtained from lettuce and spearmint shoots when cultured in 1-quart Mason jars containing 100- or 150-ml aliquots of medium
compared to jars containing 25- or 50-ml aliquots of medium within an environment containing either 350 or 10,000 μmol mol–1 CO2. High culture density decreased growth yields, and this phenomenon could only be slightly off-set by the employment of an
elevated CO2 environment or larger culture vessels.
Received: 22 December 1998 / Revision received: 2 July 1999 / Accepted: 12 July 1999 相似文献
16.
Tetsuya Uchikoba Shigeko Fukumoto Michio Onjo Michiko Okubo Kazunari Arima Hiroo Yonezawa 《Journal of thermal biology》2003,28(8):555-562
Freesia protease (FP)-A has been found in regular freesia corms (Kaneda et al., Biosci. Biotechnol. Biochem. 61 (1997) 1554). New corms were generated from original corms that were kept for several months at 4°C. In this study, two proteases (FP-B and FP-C) have been found to new corms kept for 6 months at 4°C, and have increased during new corms enlargement.
FPs were purified from the extracts of new corms, and the Mr of those were 24k (A), 25k (B), and 24.5k (C) by SDS-PAGE, respectively.
The N-terminal sequences of FPs were identical to those of papain with respect to the conservative residues of cysteine protease. The sequence of FP-A was identical with those of FP-B within 20 residues of its N-terminal. It may be possible that FP-B was produced by some post-translational modifications from FP-A during the chilling. On the other hand, N-terminal sequence of FP-C was different from those of FP-A and FP-B. It was explained that FP-C was a new protease of freesia corm. 相似文献
17.
G. Besnard Y. Griveau M. C. Quillet H. Serieys P. Lambert D. Vares A. Bervillé 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1997,94(1):131-138
A method based upon targetting of intro-gressed markers in a Phomopsis-resistant line (R) of cultivated sunflower, issuing
from a H. argophyllus cross was used to mark the Phomopsis resistance regions. Our study was based upon 203 families derived from a cross between an inbred line susceptible to Phomopsis (S1) and the introgressed resistant line (R).
Families were checked for Phomopsis resistance level in a design with replicated plots and natural infection was re-inforced
by pieces of contaminated stems. Thirty four primers were employed for RAPD analysis. Out of 102 polymorphic fragments between
(S1) and H. argophyllus, seven were still present in (R) suggesting that they marked introgressions of H. argophyllus into (R). The plants were scored for the presence or absence of 19 fragments obtained from five primers, and the relationships between
the presence/absence of fragments in plants and Phomopsis resistance/susceptiblity in the progenies was determined by using an analysis of variance. We found that at least two introgressed regions, as well as favourable
factors from sunflower, contributed to the level of Phomopsis resistance in cultivated sunflower.
Received: 28 June 1996 / Accepted: 5 July 1996 相似文献
18.
19.
RFLP mapping of resistance to chlorosis induction by Pyrenophora tritici-repentis in wheat 总被引:2,自引:0,他引:2
J. D. Faris J. A. Anderson L. J. Francl J. G. Jordahl 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1997,94(1):98-103
Tan spot, caused by Pyrenophora tritici-repentis, is an economically important disease in major wheat production areas. The fungus can produce two genetically distinct symptoms
on leaves of susceptible wheat genotypes: tan necrosis (nec) and extensive chlorosis (chl). Our objectives were to determine
the number of genes conditioning resistance to tan spot in a population of wheat recombinant inbred lines, and map the chromosomal
location of the resistance genes using RFLPs. Conidia produced by the P. tritici-repentis isolate Pti2 (nec+chl+) were used to inoculate seedlings of 135 recombinant inbred lines derived from the cross of the synthetic
hexaploid wheat W-7984 with Opata 85. A subset of the population was inoculated with conidia produced by the isolates D308
(nec−chl+) and 86-124 (nec+chl−). Inoculated seedlings were rated on a scale of 1 to 5 based on lesion type. Necrosis-inducing
culture filtrate produced by the isolate 86-124 was also used to screen the entire population. A map consisting of 532 markers
was employed to identify significant associations between marker loci and tan spot resistance. The entire population was insensitive
to culture filtrate produced by the isolate 86-124, and the entire subset was resistant to conidial inoculation of the same
isolate. The population segregated for reaction to isolates D308 and Pti2, indicating that this population segregates for
resistance to extensive chlorosis only, and not to tan necrosis. RFLP analysis indicated the presence of a gene with a major
effect in 1AS, a gene with a minor effect in 4AL, and an interaction between the 1AS gene and a gene in 2DL. Together, these
loci explained 49.0% of the variation in this population for resistance to tan spot produced by the isolate Pti2. Two regions
one in 1BL and one in 3BL, were significantly associated with resistance to extensive chlorosis, but were not significant
in the multiple regression model. It should be feasible to introgress these resistance loci into adapted genetic backgrounds
by using a marker-assisted selection scheme.
Received: 30 March 1996 / Accepted: 31 May 1996 相似文献
20.
L. Verdoodt A. Van Haute I. J. Goderis K. De Witte J. Keulemans W. Broothaerts 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1998,96(2):294-300
To obtain homozygous genotypes of apple, we have induced haploid development of either the female or the male gametes by
parthenogenesis in situ and anther culture, respectively. Of the shoots obtained, which were mainly of a non-haploid nature,
some could be derived from fertilised egg cells or from sporophytic anther tissue. In order to select the shoots having a
true haploid origin, and thus homozygotes, we decided to use the single multi-allelic self-incompatibility gene as a molecular
marker to discriminate homozygous from heterozygous individuals. The rationale behind this approach was that diploid apple
cultivars contain 2 different alleles of the S-gene and therefore the haploid induced shoots obtained from them should have only one of the alleles of the single parent.
The parental cultivars used were ‘Idared’ (parthenogenesis in situ) and ‘Braeburn’ (androgenesis), and their S-genotypes were known, except for 1 of the ‘Braeburn’S-alleles. To stimulate parthenogenetic development ‘Idared’ styles were pollinated with irradiated ‘Baskatong’ pollen, the
S-alleles of the latter (2n) cultivar were also unknown. The cloning and sequence analysis of these 3 unidentified S-alleles, 1 from ‘Braeburn’ and 2 from ‘Baskatong’ is described, and we show that they correspond to the S
24
-, S
26
- and S
27
-alleles. We have optimised a method for analysis of the S-alleles of ‘Idared/Baskatong’- or ‘Braeburn’-derived in vitro plant tissues and have shown that this approach can be applied
for the screening of the in vitro shoots for their haploid origin.
Received: 18 August 1997 / Accepted: 10 September 1997 相似文献