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201.
SEXUALLY SELECTED TRAITS EVOLVE POSITIVE ALLOMETRY WHEN SOME MATINGS OCCUR IRRESPECTIVE OF THE TRAIT
Lutz Fromhage Hanna Kokko 《Evolution; international journal of organic evolution》2014,68(5):1332-1338
Positive allometry of secondary sexual traits (whereby larger individuals have disproportionally larger traits than smaller individuals) has been called one of the most pervasive and poorly understood regularities in the study of animal form and function. Its widespread occurrence is in contrast with theoretical predictions that it should evolve only under rather special circumstances. Using a combination of mathematical modeling and simulations, here we show that positive allometry is predicted to evolve under much broader conditions than previously recognized. This result hinges on the assumption that mating success is not necessarily zero for males with the lowest trait values: for example, a male who lacks horns or antlers might still be able to copulate if encountering an unguarded female. We predict the strongest positive allometry when males typically (but not always) compete in large groups, and when trait differences decisively determine the outcome of competitive interactions. 相似文献
202.
Graziella Hanna Pereira Aline Queiroz Santos Miriam Park Patricia Rady Muller Soraia Padua Raquel Ferrari Marchesi Vera Lucia Aldred 《Mycopathologia》2010,170(4):259-261
Paracoccidioides brasiliensis rarely shows bone marrow involvement and its response to treatment with itraconazole in children needs further assessment. We describe here a child with a juvenile disseminated form of paracoccidioidomycosis, which showed reticuloendothelial system involvement and the presence of Paracoccidioides brasiliensis in the bone marrow. The patient showed an effective and rapid response to itraconazole therapy. 相似文献
203.
Hanna Lawnicka Magdalena Kowalewicz-Kulbat Paulina Sicinska Zygmunt Kazimierczuk Pawel Grieb Henryk Stepien 《Cell and tissue research》2010,340(2):371-379
Several studies indicate the involvement of protein kinases in the progression of various malignancies. Kinase inhibitors
are therefore becoming important anticancer drugs. CK2 kinase (casein kinase-2) has been suggested to be a constituent of
a neoplastic milleu, and its inhibition might represent a new approach to cancer therapy. Adrenocortical carcinomas (ACCs)
are highly malignant neoplasms with poor overall prognosis. We have examined the effects of 2-dimethylamino-4,5,6,7-tetrabromobenzimidazole
(DMAT), a potent CK2 inhibitor, on the H295R human adrenocortical cancer cell line. Treatment with DMAT decreases the secretion
of aldosterone, dehydroepiandrosterone sulfate, and androstendione and results in an accumulation of 17-OH-progesterone. Cell
growth as measured by the MTT and 5-bromo-2′-deoxyuridine incorporation assays is inhibited, and cell cycle analysis has revealed
a slight induction of apoptosis. Thus, CK2 kinase activity is probably involved in human ACC endocrine activity and growth. 相似文献
204.
Hanna Mannell Ariane Hammitzsch Ramona Mettler Ulrich Pohl Florian Krtz 《Cellular signalling》2010,22(1):88-96
Angiogenesis initiation is crucially dependent on endothelial proliferation and can be stimulated by the fibroblast growth factor 2 (FGF-2). The DNA dependent protein kinase (DNA-PK), long known for its importance in repairing DNA double strand breaks, belongs to the phosphatidylinositol-3 kinase (PI3-K) super family and has recently been identified as one of the enzymes phosphorylating and activating Akt. Due to its similarity with PI3-K, we hypothesized that DNA-PK may have similar effects on endothelial angiogenic processes and signalling. We used primary endothelial cells (HUVEC and PAEC) and human microvascular endothelial cells (HMEC) to study the role of DNA-PK in endothelial proliferation and signalling. DNA-PKcs suppression with the compound NU7026 or with siRNA induced basal endothelial cell proliferation as well as enhanced FGF-2 dependent proliferation. This was associated with an increase in phosphorylated Akt. Tube formation was not affected by DNA-PKcs clearly showing that the role of DNA-PK in endothelial processes differs from that of PI3-K. Our findings indicate DNA-PK as an important enzyme maintaining the quiescent endothelial phenotype by actively inhibiting Akt thus restraining endothelial cell proliferation preventing excessive growth. 相似文献
205.
206.
A basic premise of conservation geneticists is that low levels of genetic variation are associated with fitness costs in terms
of reduced survival and fecundity. These fitness costs may frequently vary with environmental factors and should increase
under more stressful conditions. However, there is no consensus on how fitness costs associated with low genetic variation
change under natural conditions in relation to the stressfulness of the environment. On the Swedish west coast, natterjack
toad Bufo calamita populations show a strong population genetic structure and large variation in the amount of within-population genetic variation.
We experimentally examined the survival of natterjack larvae from six populations with different genetic variation in three
thermal environments corresponding to (a) the mean temperature of natural ponds (stable, laboratory), (b) a high temperature
environment occurring in desiccating ponds (stable, laboratory) and (c) an outdoor treatment mimicking the natural, variable
thermal conditions (fluctuating, semi-natural). We found that larvae in the outdoor treatment had poorer survival than larvae
in the stable environments suggesting that the outdoor treatment was more stressful. Overall, populations with higher genetic
variation had higher larval survival. However, a significant interaction between treatments and genetic variation indicated
that fitness costs associated with low genetic variation were less severe in the outdoor treatment. Thus, we found no support
for the hypothesis that fitness costs associated with low genetic variation increase under more stressful conditions. Our
results suggest that natural thermal stress may mask fitness losses associated with low genetic variation in these populations. 相似文献
207.
Vicky P. K. H. Nguyen George Hanna Natalie Rodrigues Katerina Pizzuto Eric Yang Paul Van Slyke Harold Kim Stephen H. Chen Daniel J. Dumont 《Proteomics》2010,10(8):1658-1672
Differential protein profiling by 2‐D PAGE is generally useful in biomarker discovery, proteome analysis and routine sample preparation prior to analysis by MS. The goal of this study was to compare 2‐D PAGE‐resolved protein profile of lymphatic endothelial cells to those of venous, and arterial endothelial cells isolated from lymphatic and blood vessels of bovine mesentery (bm). Three 2‐D PAGE electrophoretograms were produced for each of the three cell types and quantitatively analyzed. Protein identification by LC‐MS/MS was performed to identify 39 proteins found to be present at statistically significantly different levels in the three cell types (p<0.05). Most of the 39 proteins have not been previously reported in EC proteomic studies of 2‐D PAGE electrophoretograms. Three proteins, HSPA1B (HSP70 family member), HSPB1 (HSP27 family member), and UBE2D3 (a member of E2 ubiquitin‐conjugating enzymes) found to be at highest levels in bm arterial endothelial cells, bm venous endothelial cells, and bm lymphatic endothelial cells, respectively, were validated by immunoblotting with appropriate antibodies. The lack of substantial overlap between our results and those of other groups' comparative studies are discussed. Functional implications of differences in levels of various proteins identified in the three cell types are also discussed. 相似文献
208.
Recently, Eskola and Geritz (Bull. Math. Biol. 69:329–346, 2007) showed that several discrete-time population models can be derived mechanistically within a single ecological framework
by varying the within-season patterns of reproduction and inter-individual aggression. However, these models do not have the
Allee effect. In this paper, we modify the original modelling framework by adding different mate finding processes, and thus
derive mechanistically several population models with the Allee effect. 相似文献
209.
Leana Doherty Adrianna Vlachos Valerie Choesmel Marie-Françoise O'Donohue Catherine Clinton Colin A. Sieff Peter E. Newburger Edyta Niewiadomska Bertil Glader Jason E. Farrar Jeffrey M. Lipton Pierre-Emmanuel Gleizes Hanna T. Gazda 《American journal of human genetics》2010,86(2):222-6951
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia that usually presents before the first birthday or in early childhood, is associated with birth defects and an increased risk of cancer. Although anemia is the most prominent feature of DBA, the disease is also characterized by growth retardation and congenital malformations, in particular craniofacial, upper limb, heart, and urinary system defects that are present in ∼30%–50% of patients. DBA has been associated with mutations in seven ribosomal protein (RP) genes, RPS19, RPS24, RPS17, RPL35A, RPL5, RPL11, and RPS7, in about 43% of patients. To continue our large-scale screen of RP genes in a DBA population, we sequenced 35 ribosomal protein genes, RPL15, RPL24, RPL29, RPL32, RPL34, RPL9, RPL37, RPS14, RPS23, RPL10A, RPS10, RPS12, RPS18, RPL30, RPS20, RPL12, RPL7A, RPS6, RPL27A, RPLP2, RPS25, RPS3, RPL41, RPL6, RPLP0, RPS26, RPL21, RPL36AL, RPS29, RPL4, RPLP1, RPL13, RPS15A, RPS2, and RPL38, in our DBA patient cohort of 117 probands. We identified three distinct mutations of RPS10 in five probands and nine distinct mutations of RPS26 in 12 probands. Pre-rRNA analysis in lymphoblastoid cells from patients bearing mutations in RPS10 and RPS26 showed elevated levels of 18S-E pre-rRNA. This accumulation is consistent with the phenotype observed in HeLa cells after knockdown of RPS10 or RPS26 expression with siRNAs, which indicates that mutations in the RPS10 and RPS26 genes in DBA patients affect the function of the proteins in rRNA processing. 相似文献
210.
Sandra Andorf Joachim Selbig Thomas Altmann Kathrin Poos Hanna Witucka-Wall Dirk Repsilber 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2010,120(2):249-259
Heterosis is a well-known phenomenon but the underlying molecular mechanisms are not yet established. To contribute to the
understanding of heterosis at the molecular level, we analyzed genome-wide gene expression profile data of Arabidopsis thaliana in a systems biological approach. We used partial correlations to estimate the global interaction structure of regulatory
networks. Our hypothesis states that heterosis comes with an increased number of partial correlations which we interpret as
increased numbers of regulatory interactions leading to enlarged adaptability of the hybrids. This hypothesis is true for
mid-parent heterosis for our dataset of gene expression in two homozygous parental lines and their reciprocal crosses. For
the case of best-parent heterosis just one hybrid is significant regarding our hypothesis based on a resampling analysis.
Summarizing, both metabolome and gene expression level of our illustrative dataset support our proposal of a systems biological
approach towards a molecular basis of heterosis. 相似文献