311 research outputs found

    Strong Robustness of Randomized Rumor Spreading Protocols

    Full text link
    Randomized rumor spreading is a classical protocol to disseminate information across a network. At SODA 2008, a quasirandom version of this protocol was proposed and competitive bounds for its run-time were proven. This prompts the question: to what extent does the quasirandom protocol inherit the second principal advantage of randomized rumor spreading, namely robustness against transmission failures? In this paper, we present a result precise up to (1±o(1))(1 \pm o(1)) factors. We limit ourselves to the network in which every two vertices are connected by a direct link. Run-times accurate to their leading constants are unknown for all other non-trivial networks. We show that if each transmission reaches its destination with a probability of p(0,1]p \in (0,1], after (1+\e)(\frac{1}{\log_2(1+p)}\log_2n+\frac{1}{p}\ln n) rounds the quasirandom protocol has informed all nn nodes in the network with probability at least 1-n^{-p\e/40}. Note that this is faster than the intuitively natural 1/p1/p factor increase over the run-time of approximately log2n+lnn\log_2 n + \ln n for the non-corrupted case. We also provide a corresponding lower bound for the classical model. This demonstrates that the quasirandom model is at least as robust as the fully random model despite the greatly reduced degree of independent randomness.Comment: Accepted for publication in "Discrete Applied Mathematics". A short version appeared in the proceedings of the 20th International Symposium on Algorithms and Computation (ISAAC 2009). Minor typos fixed in the second version. Proofs of Lemma 11 and Theorem 12 fixed in the third version. Proof of Lemma 8 fixed in the fourth versio

    The stable roommates problem with globally-ranked pairs

    Get PDF
    We introduce a restriction of the stable roommates problem in which roommate pairs are ranked globally. In contrast to the unrestricted problem, weakly stable matchings are guaranteed to exist, and additionally, they can be found in polynomial time. However, it is still the case that strongly stable matchings may not exist, and so we consider the complexity of finding weakly stable matchings with various desirable properties. In particular, we present a polynomial-time algorithm to find a rank-maximal (weakly stable) matching. This is the first generalization of an algorithm due to [Irving et al. 06] to a nonbipartite setting. Also, we describe several hardness results in an even more restricted setting for each of the problems of finding weakly stable matchings that are of maximum size, are egalitarian, have minimum regret, and admit the minimum number of weakly blocking pairs

    Effects of a saponin fraction extracted from Trigonella foenum-graecum L. and two commercially available saponins on sex ratio and gonad histology of Nile tilapa fry, Oreochromis niloticus (L.)

    Get PDF
    Over three million tonnes (t) of tilapia, mostly Nile tilapia (Oreochromis niloticus, L.), are produced annually making it the second most abundantly produced freshwater fish (FAO, 2010). Tilapia are mouthbreeders that often produce stunted populations under pond conditions; one means of prevention is to produce all-male fish with the additional advantage that males usually grow faster than females. All-male populations can be achieved by supplementing feed with androgens such as 17-α-Methyltestosterone (MT) during days 10–25 post-hatch (Pandian and Sheela, 1995). However, MT is considered to be carcinogenic (Velazquez and Alter, 2004), and Hulak et al. (2008) also showed that effluents of systems in which carp were fed diets containing MT caused masculinization of female fish. Furthermore, in aquaculture the application of hormones to fish destined for human consumption is prohibited in the European Union under directive 96/22/EC, article 5, which also prohibits import of animal products produced with hormones. Kwon et al. (2000) showed that Fadrozole, a non-steroidal compound, caused masculinization in tilapia by inhibiting aromatase, which is the enzyme responsible for the conversion of endogenous androgens to estrogens. Steinbronn et al. (2004) were able to show that a dose of 2000 ppm Quillaja saponins (Sigma S-2149) inhibited reproduction of tilapia after dietary application for 32 days to first-feeding fry, suggesting saponins as a possible alternative to MT. These secondary plant compounds consist of either a steroid or triterpenoid basic structure (aglycone or sapogenin) plus one or more sugar side chains (Francis et al., 2002a). In a previous experiment a saponin fraction from the soapbark tree (Quillaja saponaria M.) inhibited aromatase in vitro (Golan et al., 2008). The fenugreek plant (Trigonella foenum-graecum L), widely cultivated in the Middle East and Asia, also has a high saponin content. The experiment was therefore conducted to test whether saponin fractions from Q. saponaria and from T. foenum-graecum were able to influence the sex ratio and gonad histology of Nile tilapia

    Gonadotropins in the Russian Sturgeon: Their Role in Steroid Secretion and the Effect of Hormonal Treatment on Their Secretion.

    Get PDF
    In the reproduction process of male and female fish, pituitary derived gonadotropins (GTHs) play a key role. To be able to specifically investigate certain functions of Luteinizing (LH) and Follicle stimulating hormone (FSH) in Russian sturgeon (Acipenser gueldenstaedtii; st), we produced recombinant variants of the hormones using the yeast Pichia pastoris as a protein production system. We accomplished to create in vitro biologically active heterodimeric glycoproteins consisting of two associated α- and β-subunits in sufficient quantities. Three dimensional modelling of both GTHs was conducted in order to study the differences between the two GTHs. Antibodies were produced against the unique β-subunit of each of the GTHs, in order to be used for immunohistochemical analysis and to develop an ELISA for blood and pituitary hormone quantification. This detection technique revealed the specific localization of the LH and FSH cells in the sturgeon pituitary and pointed out that both cell types are present in substantially higher numbers in mature males and females, compared to immature fish. With the newly attained option to prevent cross-contamination when investigating on the effects of GTH administration, we compared the steroidogeneic response (estradiol and 11-Keto testosterone (11-KT) in female and males, respectively) of recombinant stLH, stFSH, and carp pituitary extract in male and female sturgeon gonads at different developmental stages. Finally, we injected commercially available gonadotropin releasing hormones analog (GnRH) to mature females, and found a moderate effect on the development of ovarian follicles. Application of only testosterone (T) resulted in a significant increase in circulating levels of 11-KT whereas the combination of GnRH + T did not affect steroid levels at all. The response pattern for estradiol demonstrated a similar situation. FSH levels showed significant increases when GnRH + T was administered, while no changes were present in LH levels

    Regulation of Gonadotropin-Releasing Hormone (GnRH)-Receptor Gene Expression in Tilapia: Effect of GnRH and Dopamine

    Get PDF
    The present work was designed to study certain aspects of the endocrine regulation of gonadotropin-releasing hormone receptor (GnRH-R) in the pituitary of the teleost fish tilapia. A GnRH-R was cloned from the pituitary of hybrid tilapia (taGnRH-R) and was identified as a typical seven-transmembrane receptor. Northern blot analysis revealed a single GnRH-R transcript in the pituitary of approximately 2.3 kilobases. The taGnRH-R mRNA levels were significantly higher in females than in males. Injection of the salmon GnRH analog (sGnRHa; 5–50 μg/kg) increased the steady-state levels of taGnRH-R mRNA, with the highest response recorded at 25 μg/kg and at 36 h. At the higher dose of sGnRHa (50 μg/kg), taGnRH-R transcript appeared to be down-regulated. Exposure of tilapia pituitary cells in culture to graded doses (0.1–100 nM) of seabream (sbGnRH = GnRH I), chicken II (cGnRH II), or salmon GnRH (sGnRH = GnRH III) resulted in a significant increase in taGnRH-R mRNA levels. The highest levels of both LH release and taGnRH-R mRNA levels were recorded after exposure to cGnRH II and the lowest after exposure to sbGnRH. The dopamine-agonist quinpirole suppressed LH release and mRNA levels of taGnRH-R, indicating an inhibitory effect on GnRH-R synthesis. Collectively, these data provide evidence that GnRH in tilapia can up- regulate, whereas dopamine down-regulates, taGnRH-R mRNA levels

    Spawning Induction in the Carp: Past Experience and Future Prospects - A Review

    Get PDF
    Most fish in aquaculture either fail to breed in captivity or their spawning occurs sporadically and late in the season. This is mainly due to the lack of natural cues in captivity, which leads to dysfunction of the endocrine axis regulating oocyte maturation and ovulation. Hypophysation as a remedy for this situation in fish has been employed in aquaculture since the 1930s and is still widely practiced. However, using crude pituitary homogenates in local hatcheries has frequently ended in failures that were attributed to the incon- sistent potency of the injected material and the unknown ovarian stage of the recipient fish. Since the mid 1980s, hypophysation has improved through the introduction of a standardized dry carp pituitary extract in which the luteinizing hormone (LH) content and activity have been calibrated (cal- ibrated carp pituitary extract = CCPE). Induction of spawning, however, is successful mainly in female cohorts in which 65% or more of the oocytes in an ovarian biopsy have migrating germinal vesicles. Further, due to decreasing quantities of industry-processed common carp and the expan- sion of ornamental carp production (koi and goldfish), the growing demand for CCPE could not be met, and an alternative had to be found. A hypo- thalamic approach, introduced into Israeli aquaculture in 1993 (called Dagin), combines a superactive analog of sGnRH (10 μg/kg), with the water-soluble dopamine (D2) receptor antagonist, metoclopramide (20 mg/kg). The progress of oocyte maturation in ovarian biopsies has been studied in parallel with changes in levels of LH, estradiol, and the matura- tion-inducing steroid (MIS; 17α, 20β, dihydroxy-4-pregnene-3-one). The hormone profile indicated that the gradual increases in LH and MIS follow- ing a single administration of Dagin were similar to those in fish treated with priming and resolving doses of CCPE. This would explain why Dagin is effective even when only a single injection is given, saving labor and reduc- ing handling stress. CCPE and Dagin were tested in parallel on common carp in a commercial hatchery. The spawning ratio and embryo viability were similar, although the latency between injection and ovulation was con- siderably longer and more variable in Dagin-treated than in CCPE-treated carp. It is recommended to use CCPE at the beginning and end of the spawning season when the LH content in the pituitary is low, and Dagin in mid-season and in field spawning. Future prospects raise the possibility that by employing molecular tools, a recombinant carp LH will be produced that will have the regular and expected potency of the hypophyseal approach without the risk of spreading pathogens from donor fish to broodstock. Work along this line is currently in progress

    Revealing genes associated with vitellogenesis in the liver of the zebrafish (Danio rerio) by transcriptome profiling

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>In oviparous vertebrates, including fish, vitellogenesis consists of highly regulated pathways involving 17β-estradiol (E2). Previous studies focused on a relatively small number of hepatic expressed genes during vitellogenesis. This study aims to identify hepatic genes involved in vitellogenesis and regulated by E2, by using zebrafish microarray gene expression profiling, and to provide information on functional distinctive genes expressed in the liver of a vitellogenic female, using zebrafish as a model fish.</p> <p>Results</p> <p>Genes associated with vitellogenesis were revealed by the following paired t-tests (SAM) comparisons: a) two-month old vitellogenic (Vit2) females were compared with non-vitellogenic (NV) females, showing 825 differentially expressed transcripts during early stages of vitellogenesis, b) four-month old vitellogenic (Vit4) females were compared with NV females, showing 1,046 differentially expressed transcripts during vitellogenesis and c) E2-treated males were compared with control males, showing 1,828 differentially expressed transcripts regulated by E2. A Venn diagram revealed 822 common transcripts in the three groups, indicating that these transcripts were involved in vitellogenesis and putatively regulated by E2. In addition, 431 transcripts were differentially expressed in Vit2 and Vit4 females but not in E2-treated males, indicating that they were putatively not up-regulated by E2. Correspondence analysis showed high similarity in expression profiles of Vit2 with Vit4 and of NV females with control males. The E2-treated males differed from the other groups. The repertoire of genes putatively regulated by E2 in vitellogenic females included genes associated with protein synthesis and reproduction. Genes associated with the immune system processes and biological adhesion, were among the genes that were putatively not regulated by E2. E2-treated males expressed a large array of transcripts that were not associated with vitellogenesis.</p> <p>The study revealed several genes that were not reported before as being regulated by E2. Also, the hepatic expression of several genes was reported here for the first time.</p> <p>Conclusion</p> <p>Gene expression profiling of liver samples revealed 1,046 differentially expressed transcripts during vitellogenesis of which at least ~64% were regulated by E2. The results raise the question on the regulation pattern and temporal pleiotropic expression of hepatic genes in vitellogenic females.</p

    Kisspeptin antagonists reveal kisspeptin 1 and kisspeptin 2 differential regulation of reproduction in the teleost, Morone saxatilis

    Get PDF
    The importance of kisspeptin in regulating vertebrate reproduction has been well established, but the exact mechanism continues to unfold. Unlike mammals, many lower vertebrates possess a dual kisspeptin system, Kiss1 and Kiss2. To decipher the roles of the kisspeptins in fish, we identified two potential kisspeptin antagonists, pep 234 and pep 359, by screening analogs for their ability to inactivate striped bass Kiss1 and Kiss2 receptors expressed in COS7 cells. Pep 234 (a mammalian KISS1 antagonist) antagonizes Kiss1r signaling activated by Kiss1 and Kiss2, and pep 359 (a novel analog) antagonizes Kiss2 activation of both receptors. In vitro studies using brain slices demonstrated that only Kiss2 can upregulate the expression of the hypophysiotropic gnrh1, which was subsequently diminished by pep 234 and pep 359. In primary pituitary cell cultures, the two antagonists revealed a complex network of putative endogenous and exogenous regulation by kisspeptin. While both kisspeptins stimulate Fsh expression and secretion, Kiss2 predominately induces Lh secretion. Pep 234 and 359 treatment of spawning males hindered sperm production. This effect was accompanied with decreased brain gnrh1 and gnrh2 mRNA levels and peptide content in the pituitary, and increased levels of pituitary Lh, probably due to attenuation of Lh release. Strikingly, the mRNA levels of arginine-vasotocin, the neurons of which in the preoptic area coexpress kiss2r, were dramatically reduced by the antagonists. Our results demonstrate differential actions of Kiss1 and Kiss2 systems along the hypothalamicpituitary axis and interactions with other neuropeptides, and further reinforce the importance of kisspeptin in the execution of spawning.The National Science Foundation program grant 1147118 and by research award IS-4499-12CR from the United States-Israel Binational Agricultural Research and Development Fund.http://www.biolreprod.org2016-09-30hb2016Mammal Research InstituteZoology and Entomolog
    corecore