The synaptic behaviour of the wild forms of Triticum turgidum and T. timopheevii

Genome ◽  
2001 ◽  
Vol 44 (4) ◽  
pp. 517-522 ◽  
Author(s):  
M Martínez ◽  
T Naranjo ◽  
C Cuadrado ◽  
C Romero

Different wild allopolyploid species of Triticeae show extensive bivalent formation at zygotene while a considerable number of multivalents is present in cultivated polyploid wheats. To study the chromosome behaviour at early meiotic stages in wild forms of tetraploid wheats Triticum turgidum and T. timopheevii (2n = 4x = 28) we have analysed the synaptic pattern in fully traced spread nuclei at mid- and late zygotene and at pachytene of wild accessions of these species. The mean number of synaptonemal complex (SC) bivalents at mid-zygotene ranged from 12.22 to 13.14 among the accessions studied indicating a strong restriction of synapsis initiation to homologous chromosomes. The mean of bivalents increased at pachytene because of the transformation of multivalents into bivalents. Ring bivalents observed at metaphase I support that SC bivalents were formed by homologous chromosomes. The average values of SC bivalents at mid-zygotene in the wild forms are much higher than the average values observed in the cultivated tetraploid wheats but similar to that of a mutant line of T. turgidum with a duplication that includes Ph1, the major homoeologous pairing suppressor locus. These results suggest that the efficiency of the mechanism operating in the homologous recognition for synapsis is higher in wild wheat populations than in cultivated varieties. Apparently, a relatively detrimental modification of the pairing regulating genetic system accompanied the domestication of the wild wheat forms.Key words: Ph1 locus, Triticum turgidum, Triticum timopheevii, synaptonemal complex, diploidisation.

Genetics ◽  
1984 ◽  
Vol 106 (2) ◽  
pp. 309-324
Author(s):  
Anne Crossway ◽  
Jan Dvořák

ABSTRACT Metaphase I (MI) pairing of wheat homologous chromosomes is usually reduced in hybrids between cultivars relative to the parental inbred lines. Previous work suggested that this phenomenon is caused by polymorphism in nucleotide sequences (nonstructural chromosome variation) among wheat cultivars. The present work investigated the distribution of this variation along three selected chromosome arms between cultivars Chinese Spring and Cheyenne. Chinese Spring ditelosomics 3Aq, 6Ap and 6Bp were crossed with disomic substitutions of Cheyenne chromosomes 3A, 6A and 6B in Chinese Spring, respectively. The resulting F1 plants, called substituted monotelodisomics, were crossed with the respective Chinese Spring monosomics, producing potentially "recombinant" substituted monosomics. When these "recombinant" chromosomes were combined with the parental Chinese Spring telosomes, marked reductions in mean telosome-pairing frequency were found compared with the corresponding Chinese Spring monotelodisomics. The mean pairing frequencies of the "recombinant" chromosomes showed a continuous distribution between those of the substituted and Chinese Spring monotelodisomics. The results suggest that the nonstructural variation that reduces MI pairing between chromosomes of different wheat cultivars is not localized in a specific site but distributed along each chromosome arm. Little variation was found among monotelodisomics for either the number of ring bivalents per cell or the number of univalents other than those constituting the heteromorphic pair. This implies that the reductions in MI pairing between the Cheyenne and Chinese Spring chromosomes are caused by something residing within these specific chromosomes that does not affect the pairing of the remaining Chinese Spring chromosomes in the same cell. Furthermore, the absence of parental types among the "recombinant"-substituted monotelodisomics suggests that the sequences involved in the variation studied here are capable of converting heterohomologous chromosomes to something intermediate in nature in the span of only a single generation.


Author(s):  
T. Guha ◽  
A. Q. Siddiqui ◽  
P. F. Prentis

The Primary Spermatocytes represent a stage in spermatogenesis when the first meiotic cell division occurs. They are derived from Spermatogonium or Stem cell through mitotic division. At the zygotene phase of meiotic prophase the Synaptonemal complex appears in these cells in the space between the paired homologous chromosomes. Spermatogenesis and sperm structure in fish have been studied at the electron microscope level in a few species? However, no work has yet been reported on ultrastructure of tilapia, O. niloticus, spermatozoa and spermatogenetic process. In this short communication we are reporting the Ultrastructure of Primary Spermatocytes in tilapia, O. niloticus, and the fine structure of synaptonemal complexes seen in the spermatocyte nuclei.


Genetics ◽  
2003 ◽  
Vol 163 (2) ◽  
pp. 539-544 ◽  
Author(s):  
Hasanuzzaman Bhuiyan ◽  
Gunilla Dahlfors ◽  
Karin Schmekel

Abstract The synaptonemal complex (SC) keeps the synapsed homologous chromosomes together during pachytene in meiotic prophase I. Structures that resemble stacks of SCs, polycomplexes, are sometimes found before or after pachytene. We have investigated ndt80 mutants of yeast, which arrest in pachytene. SCs appear normal in spread chromosome preparations, but are only occasionally found in intact nuclei examined in the electron microscope. Instead, large polycomplexes occur in almost every ndt80 mutant nucleus. Immunoelectron microscopy using DNA antibodies show strong preferential labeling to the lateral element parts of the polycomplexes. In situ hybridization using chromosome-specific probes confirms that the chromosomes in ndt80 mutants are paired and attached to the SCs. Our results suggest that polycomplexes can be involved in binding of chromosomes and possibly also in synapsis.


2020 ◽  
Author(s):  
Spencer G. Gordon ◽  
Lisa E. Kursel ◽  
Kewei Xu ◽  
Ofer Rog

AbstractDuring sexual reproduction the parental homologous chromosomes find each other (pair) and align along their lengths by integrating local sequence homology with large-scale contiguity, thereby allowing for precise exchange of genetic information. The Synaptonemal Complex (SC) is a conserved zipper-like structure that assembles between the homologous chromosomes. This phase-separated interface brings chromosomes together and regulates exchanges between them. However, the molecular mechanisms by which the SC carries out these functions remain poorly understood. Here we isolated and characterized two mutations in the dimerization interface in the middle of the SC zipper in C. elegans. The mutations perturb both chromosome alignment and the regulation of genetic exchanges. Underlying the chromosome-scale phenotypes are distinct alterations to the way SC subunits interact with one another. We propose that the SC brings homologous chromosomes together through two biophysical activities: obligate dimerization that prevents assembly on unpaired chromosomes; and a tendency to phase-separate that extends pairing interactions along the entire length of the chromosomes.


Author(s):  
Fabio Castaño Rivera ◽  
Julián Botero Arango

Two groups of adult Mutton snapper fish Lutjanus analis captured in the wild, each one of three females and four males, were kept during eight months under controlled temperature and photoperiod conditions in the lab in order to stimulate their sexual maturation which was in a state of latency because of the effects of confinement. The first group was maintained under an artificial cycle with temperature manipulation and the second under a control cycle, in which this parameter was left at natural conditions. Every two months blood samples from all females were taken for the analysis of plasma testosterone (T) and oestradiol (E2) levels, taking ovarian biopsies simultaneously to register the mean diameter of the oocytes. After six months, a significative increase in the mean diameter of the oocytes of the three females of the artificial cycle was observed, with coincidence and statistic relationship with the increase in the T and E2 (r = 0.62 y 0.82 respectively). No oocyte growth was observed in the females under the control cycle. In both, artificial and control cycles, T and E2 levels showed a close relationship with photoperiod (r = 0.84 y r = 0.61) while temperature showed a lower or non significant relationship (r = 0.40 y r = 0.20). Statistical differences (P<0.1) were found between the condition factors of the two groups, while the sexual steroids didn’t show any differences between them. The present work constitutes the first report on the analysis of sexual steroid levels during the gonadal maturation process in fish of the Family Lutjanidae kept under an artificial conditioning cycle.


1995 ◽  
Vol 18 (1) ◽  
pp. 1
Author(s):  
R.T. Gemmell

The brushtail possum is a common arboreal marsupial that is well adapted to the Australian urban environment and to rearing in captivity. Data obtained from 100 female possums housed in a semi-captive colony over a 7 year period demonstrate the reproductive capability of this marsupial. The main breeding season is from March to June with a declining number of births occurring from July to October. The possums gave birth to 259 single young and one set of twins. The range of the lactation period was from 177 to 200 days with the birth of the subsequent young occurring at 188.4 ± 4.1 days post partum (SD, n = 5). The growth rate of the young female possum varied greatly after day 100 post partum, the mean body weight of possums at day 172, being 753.0 ± 76.2g (SD, n = 5) with a range of 685 to 851 g. Female possums, with a mean body weight of 2171 ± 388g, gave birth to their first litter on day 345.9 ± 69.3 days postpartum (mean, SD, n = 7). Although two female possums trapped in the wild were held in captivity for 64 and 63.4 months and one possum bred in captivity had a life span of 51.5 months, the mean life span was 21.0 ± 12.5 months (SD, n =3D 8), with a range of 14.3 to 51.5 months. This life span is very variable and it is of interest to determine if this is an artefact of captivity or is also observed in the wild.


2020 ◽  
Vol 31 (4) ◽  
pp. 884-891 ◽  
Author(s):  
Ana Laura Dutra ◽  
Clemens Schlindwein ◽  
Reisla Oliveira

Abstract The time dedicated to courtship and copulation is the most general cost of mating for females. However, quantitative estimates of this cost and the consequences for female mating behavior have been investigated for only a few model organisms and mostly under laboratory conditions. We determined the costs of copulations and persistent courtship by males in terms of time for females of the solitary bee Anthrenoides micans. We estimated the rate and duration of male mating behaviors and the consequences for sexual interactions for females with respect to the loss of foraging opportunity in the wild. Males invested most of their time searching for mates and intercepted foraging females every 3 min. Copulas lasted, on average, 10 times longer than the time females took to resist male mating attempts. Despite the high frequency of these rejections (82%), females spent 3-fold more time copulating than rejecting males. Considering the rate of encounters with males and the mean duration of flower visits by females, we estimated that females would perform 64% fewer flower visits per hour if they accepted all copulation attempts. The loss of time is especially significant in the natural habitat of the species, where host cacti blossom for extraordinary short periods of time and females compete with other cacti-specialized bees and conspecifics. Because the offspring production of a female solitary bee depends on its pollen collection capacity, reduced foraging performance directly influences female reproductive success.


2007 ◽  
Vol 89 (2) ◽  
pp. 93-106 ◽  
Author(s):  
NOELLE A. BARKLEY ◽  
ROB E. DEAN ◽  
ROY N. PITTMAN ◽  
MING L. WANG ◽  
CORLEY C. HOLBROOK ◽  
...  

SummaryThirty-one genomic SSR markers with a M13 tail attached were used to assess the genetic diversity of the peanut mini core collection. The M13-tailed method was effective in discriminating almost all the cultivated and wild accessions. A total of 477 alleles were detected with an average of 15·4 alleles per locus. The mean polymorphic information content (PIC) score was 0·687. The cultivated peanut (Arachis hypogaea L.) mini core produced a total of 312 alleles with an average of 10·1 alleles per locus. A neighbour-joining tree was constructed to determine the interspecific and intraspecific relationships in this data set. Almost all the peanut accessions in this data set classified into subspecies and botanical varieties such as subsp. hypogaea var. hypogaea, subsp. fastigiata var. fastigiata, and subsp. fastigiata var. vulgaris clustered with other accessions with the same classification, which lends further support to their current taxonomy. Alleles were sequenced from one of the SSR markers used in this study, which demonstrated that the repeat motif is conserved when transferring the marker across species borders. This study allowed the examination of the diversity and phylogenetic relationships in the peanut mini core which has not been previously reported.


Plant Disease ◽  
2020 ◽  
Vol 104 (2) ◽  
pp. 448-454 ◽  
Author(s):  
Niuniu Shi ◽  
Hongchun Ruan ◽  
Lin Gan ◽  
Yuli Dai ◽  
Xiujuan Yang ◽  
...  

Asparagus stem blight caused by Phomopsis asparagi is a major hindrance to asparagus production worldwide. Currently, fungicides are used to manage the disease in commercial production, but resistance to common fungicides has emerged in the wild population. In the present study, 132 isolates of P. asparagi collected from different provinces in China were tested for sensitivities to pyraclostrobin, tebuconazole, and fluazinam. We also determined the efficacies of six fungicides against P. asparagi. The frequency distributions of EC50 values of the isolates tested were unimodal, but the curves for pyraclostrobin and tebuconazole had long right-hand tails. The mean EC50 values for pyraclostrobin, tebuconazole, and fluazinam were 0.0426 ± 0.0029, 0.6041 ± 0.0416, and 0.0314 ± 0.0013 μg/ml, respectively. In addition, the EC50 values for pyraclostrobin were very similar with or without salicylhydroxamic acid (SHAM), 20 μg/ml, indicating that SHAM is not needed to determine the sensitivity of P. asparagi to pyraclostrobin when using the mycelial growth inhibition assay. In greenhouse assays, Merivon (42.4% fluxapyroxad plus pyraclostrobin SC), Frown-cide (500 g/liter fluazinam SC), Cabrio (250 g/liter pyraclostrobin EC), and Nativo (75% trifloxystrobin plus tebuconazole WG) showed excellent preventive efficacy against P. asparagi. And these fungicides were more effective before inoculation than when they were applied after inoculation (P < 0.05). Therefore, these fungicides should be applied prior to infection to control stem blight. In field trials, Frown-cide, Merivon, Nativo, and Cabrio also performed good control effects, ranging from 75.2 to 86.0% in 2017 and 75.4 to 87.1% in 2018. We demonstrated that Frown-cide, Merivon, Nativo, and Cabrio had considerable potential to manage asparagus stem blight. In addition, rotations of these fungicides are essential for precluding or delaying the development of resistance and for controlling the disease.


2018 ◽  
Vol 47 (1) ◽  
pp. 177-182 ◽  
Author(s):  
Nimet S. GENÇER ◽  
Cevriye MERT

The Asian chestnut gall wasp Dryocosmus kuriphilus is a global pest of chestnut (Castanea spp.). It has been spreading in Turkey’s forests and orchards since 2014. This pest imposes a big threat to the Turkish chestnut industry, which is among the top producers in the world. Its gall morphology has been related to pest pressure and host cultivar, thus eventually modulating plant damage with heavy impact on growth and fruit production. We compared gall characters (position on plant organ, ratios, dimensions, volumes, number of larval chambers) in wild Castanea sativa, two local cultivars and a Euro Japanese hybrid. Overall, leaf galls were more common (55.36%), followed by the stem (19.6%) and leaf stipule galls (15.29%). The mean number of chamber and volume value of gall types were 1.52-5.93 and 0.43-2.15 cm3, respectively. The highest values were observed in ‘stem gall’. The more gall formation was observed in the wild chestnut trees and ‘Marigoule’ than the other local varieties.


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