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PubMed2002

A basic helix-loop-helix protein with similarity to the fungal morphological regulators, Phd1p, Efg1p and StuA, controls conidiation but not dimorphic growth in Penicillium marneffei.

Members of the APSES protein group are basic helix-loop-helix (bHLH) proteins that regulate processes such as mating, asexual sporulation and dimorphic growth in fungi. Penicillium marneffei is a human pathogen and is the only member of its genus to display a dimorphic growth transition. At 25 degrees C, P. marneffei grows with a filamentous morphology and produces asexual spores from multicellular con-idiophores. At 37 degrees C, the filamentous morphology is replaced by yeast cells that reproduce by fission. We have cloned and characterized an APSES protein-encoding gene from P. marneffei that has a high degree of similarity to Aspergillus nidulans stuA. Deletion of stuA in P. marneffei showed that it is required for metula and phialide formation during conidiation but is not required for dimorphic growth. This suggests that APSES proteins may control processes that require budding (formation of the metulae and phialides, pseudohyphal growth in Saccharomyces cerevisiae and dimorphic growth in Candida albicans) but not those that require fission (dimorphic growth in P. marneffei). The A. nidulans DeltastuA mutant has defects in both conidiation and mating. The P. marneffei stuA gene was capable of complementing the conidiation defect but could only inefficiently complement the sexual defects of the A. nidulans mutant. This suggests that the P. marneffei gene, which comes from an asexual species, has diverged significantly from the A. nidulans gene with respect to sexual but not asexual development.

Amino Acid Sequence↗
PubMed2004

Sexual selection explains Rensch's rule of size dimorphism in shorebirds.

Sexual size dimorphism shows a remarkably widespread relationship to body size in the animal kingdom: within lineages, it decreases with size when females are the larger sex, but it increases with size when males are the larger sex. Here we demonstrate that this pattern, termed Rensch's rule, exists in shorebirds and allies (Charadriides), and it is determined by two components of sexual selection: the intensity of sexual selection acting on males and the agility of the males' display. These effects are interactive so that the effect of sexual selection on size dimorphism depends on male agility. As a control, we also examine dimorphism in bill length, which is a functionally selected trait. As such, dimorphism in bill length neither exhibits Rensch's rule nor is associated with sexual selection and display. Our results show that variation among taxa in the direction and magnitude of sexual size dimorphism, as manifested as Rensch's rule, can be explained by the interaction between the form and strength of sexual selection acting on each sex in relation to body size.

Animals↗
PubMed2004

Sexual dimorphism of rat liver nuclear proteins: regulatory role of growth hormone.

Many genes are expressed in mammalian liver in a sexually dimorphic manner. DNA microarray analysis has shown that growth hormone (GH) and its sex-dependent pattern of pituitary secretion play a major role in establishing the sexually dimorphic patterns of liver gene expression. However, GH may exert effects on protein post-translational modification and nuclear localization that are not reflected at the mRNA level. To investigate these potential effects of GH, we used two-dimensional gel electrophoresis followed by LC-MS/MS to: 1) identify rat liver nuclear proteins whose abundance or state of post-translational modification displays sex-dependent differences; and 2) determine the role of the plasma GH profile in establishing these differences. Nuclear extracts prepared from livers of individual male (n=9) and female (n=5) adult rats, and from males given GH by continuous infusion for 7 days to feminize liver gene expression (n=5 rats), were resolved by two-dimensional electrophoresis. Image analysis of SYPRO Ruby-stained gels revealed 165 sexually dimorphic protein spots that differ in normalized volume between male and female groups by >1.5-fold at p<0.05. Sixty of these proteins exhibited female-like changes in spot abundance following continuous GH treatment. Comparison of male and GH-treated male groups revealed 130 proteins that displayed >1.5-fold differences in abundance, with 60 of these GH-responsive spots being sexually dimorphic. Thus, GH plays an important role in establishing the sex-dependent differences in liver nuclear protein content. Twenty-eight of the sexually dimorphic and/or GH-regulated protein spots were identified by LC-MS/MS. Proteins identified include regucalcin, nuclear factor 45, and heterogeneous nuclear ribonucleoproteins A3, D-like, and K, in addition to proteins such as GST, normally associated with cytosolic extracts but also reported to be localized in the nucleus.

Animals↗
PubMedDate not supplied

Some multivariate tests for differences in sexual dimorphism between human populations.

Two multivariate statistical tests are presented for examining differences in sexual dimorphism between human populations. One test refers to general differences in sexual dimorphism; the other, only to differences in size aspects of sexual dimorphism. There is no current resolution to the complementary problem of testing for differences of direction in sexual dimorphism. By applying the tests to a comparison of sexual dimorphism in 26 samples of skulls from a world-wide distribution of human populations, significant results (at alpha = 0.05) were found in the majority of cases with the general test, and in a minority of cases with the size test.

Analysis of Variance↗
PubMed2005

The limits on sexual dimorphism in vegetative traits in a gynodioecious plant.

Gynodioecious plants exhibit modest sexual dimorphism in vegetative and phenological traits, which stands in stark contrast to pronounced dimorphism in reproductive traits. I evaluate the roles of limited genetic variation, negative genetic covariation (within and between sex morphs), and lack of gender-differential selection in contributing to minimal sexual dimorphism for these traits in Fragaria virginiana. Major findings are as follows. First, selection was sometimes differential but rarely divergent between male and female fertility modes. Second, response to selection was constrained by low genetic variation and extensive genetic covariance. In fact, covariance between traits within sex morphs appears to represent a constraint on par with that of covariance between sex morphs. Third, these constraints combine with different modes of gamete transmission to produce very different gender-specific contributions to the mean phenotypes of the next generation. Finally, predicted responses to selection for several traits are concordant with the degree and direction of dimorphism in a closely related dioecious species. In sum, this work suggests that minimal sexual dimorphism in vegetative and phenological traits is due to similar directional selection via male and female fertility combined with the constraints of low genetic variation and extensive genetic covariance both within and between sex morphs.

Biological Evolution↗
PubMedDate not supplied

Sexual dimorphism in physiological performance of whiptail lizards (genus Cnemidophorus).

Numerous studies have examined sexual dimorphism in the morphology and behavior of vertebrates; very few, however, have explicitly investigated the possibility of gender differences in physiological performance, despite the observations of such differences in humans. In this study, I investigated physiological sexual dimorphism in the lizard genus Cnemidophorus by measuring five whole-animal traits, all of which are likely to influence fitness in these species: burst speed, endurance, maximal exertion capacity, standard metabolic rate, and evaporative water loss rate. Because at least some of these traits are known to be strongly influenced by body size, I tested for dimorphism using both absolute and size-corrected trait values. An examination of six Cnemidophorus species and subspecies revealed a strong trend toward higher absolute trait values in males for all variables except endurance. Most of the dimorphism in standard metabolic rate and evaporative water loss rate could be explained by differences in body mass between males and females; for the locomotor traits, however, body size explained only a small fraction of the overall sexual dimorphism. The portion of trait differences not explained by body size was likely due to gender differences in physiology, such as differences in relative muscularity and fat content.

Animals↗
PubMed2001

Normal sexual dimorphism of the adult human brain assessed by in vivo magnetic resonance imaging.

The etiology and consistency of findings on normal sexual dimorphisms of the adult human brain are unresolved. In this study, we present a comprehensive evaluation of normal sexual dimorphisms of cortical and subcortical brain regions, using in vivo magnetic resonance imaging, in a community sample of 48 normal adults. The men and women were similar in age, education, ethnicity, socioeconomic status, general intelligence and handedness. Forty-five brain regions were assessed based on T(1)-weighted three-dimensional images acquired from a 1.5 T magnet. Sexual dimorphisms of adult brain volumes were more evident in the cortex, with women having larger volumes, relative to cerebrum size, particularly in frontal and medial paralimbic cortices. Men had larger volumes, relative to cerebrum size, in frontomedial cortex, the amygdala and hypothalamus. A permutation test showed that, compared to other brain areas assessed in this study, there was greater sexual dimorphism among brain areas that are homologous with those identified in animal studies showing greater levels of sex steroid receptors during critical periods of brain development. These findings have implications for developmental studies that would directly test hypotheses about mechanisms relating sex steroid hormones to sexual dimorphisms in humans.

Adult↗
PubMed2002

Dimorphic mating-type chromosomes in the fungus Microbotryum violaceum.

Fungi often mate as haploids, and sex chromosomes (i.e., mating-type chromosomes) that are dimorphic for their size or overall DNA content have never been reported in this kingdom. Using electrophoretic techniques for karyotype analysis, a highly dimorphic chromosome pair that determines mating compatibility is shown to occur in populations of the fungus Microbotryum violaceum. This substantiates the evolution of such dimorphism as a general feature associated with haploid determination of mating compatibility, which previously had been known only in haplodioecious plants (mosses and liverworts). Size-dimorphic sex chromosomes are present in a lineage of M. violaceum native to Europe, as well as a lineage native to North America. However, they are very different in size between these lineages, indicating either independent evolution of the dimorphism or a large degree of divergence since their isolation. Several DNA sequences that show sequence similarity to transposons were isolated from these sex chromosomes.

Basidiomycota↗
PubMed2002

Sexual size dimorphism in anurans.

Several hypotheses have been proposed to explain the direction and extent of sexual size dimorphism in anurans (in which males are usually smaller than females) as a result of sexual selection. Here, we present an analysis to test the hypothesis that sexual dimorphism in anurans is largely a function of differences between the sexes in life-history strategies. Morphological and demographic data for anurans were collected from the literature, and the mean size and age in each sex were calculated for 51 populations, across 30 species and eight genera. Comparisons across 14 Rana species, eight Bufo species and across the genera showed a highly significant relationship between size dimorphism, measured using the female-male size ratio, and mean female-male age difference. A comparison of a subset of 17 of these species for which phylogenetic information was available, using the method of independent contrasts, yielded a similar result. These results indicate that most of the variation in size dimorphism in the anura can be explained in terms of differences in the age structure between the sexes in breeding populations. If sexual selection has an effect on size dimorphism in anurans, it is likely to be only a secondary one.

Age Factors↗
PubMed2003

Evolution of sexual dimorphism in the olfactory brain of Hawaiian Drosophila.

In the fruitfly, Drosophila melanogaster, mate choice during courtship depends on detecting olfactory cues, sex pheromones, which are initially processed in the antennal lobe (AL), a primary olfactory centre of the brain. However, no sexual differences in the structure of the AL have been found in Drosophila. We compared the central brain anatomy of 37 species of Drosophilidae from the islands of the Hawaiian archipelago, uncovering an extreme sexual dimorphism within the AL in which two out of the 51 identifiable glomeruli were markedly enlarged in males. A phylogeny indicated that the sexual dimorphism of the homologous glomeruli arose 0.4-1.9 Myr ago independently in two species groups of Hawaiian endemic Drosophilidae. The corresponding glomeruli in D. melanogaster were also found to be sexually dimorphic. The formation of glomeruli of male size is prevented by the ectopic expression of female-type transformer (tra) cDNA in males, indicating that the glomerular sexual dimorphism is under the control of the sex-determination cascade of genes. It is suggested that a defined set of glomeruli in Drosophila can enlarge in response to sex-determination genetic signals, the mutations of which may result in species differences in sexual dimorphism of the brain.

Animals↗
PubMed2005

Estrogen regulates adrenal medullary function producing sexual dimorphism in nociceptive threshold and beta-adrenergic receptor-mediated hyperalgesia in the rat.

Epinephrine produces sexually dimorphic beta(2)-adrenergic receptor-mediated mechanical hyperalgesia, with male rats exhibiting greater hyperalgesia. Because female rats have higher plasma epinephrine levels, and beta-adrenergic receptor sensitivity is affected by chronic exposure to agonists, we tested the hypothesis that this sexual dimorphism is due to epinephrine-induced desensitization of beta(2)-adrenergic receptors. Following gonadectomy, epinephrine hyperalgesia, as measured by the Randall-Selitto paw-withdrawal test, was unchanged in male rats while in females it was increased. Prepubertal male and female rats do not demonstrate sexual dimorphism in either plasma epinephrine level or epinephrine-induced hyperalgesia. Adrenal medullectomy and adrenal denervation both significantly enhanced epinephrine hyperalgesia, but only in females. In contrast, the sexually dimorphic hyperalgesia induced by prostaglandin E(2), another agent that acts directly to sensitize primary afferent nociceptors, was not enhanced by adrenal medullectomy or denervation. Chronic administration of epinephrine in male rats, to produce plasma levels similar to those of gonad-intact females, significantly attenuated epinephrine-induced hyperalgesia, making it similar to that in females. These results strongly support the suggestion that estrogen regulates plasma epinephrine in female rats and differential sensitivity to beta(2)-adrenergic agonists accounts for the sexual dimorphism in epinephrine-induced hyperalgesia. Unexpectedly, regulation of adrenal medullary function by estrogen was also found to modulate baseline nociceptive threshold such that females had a lower nociceptive threshold.

Adrenal Medulla↗
PubMed2000

Evidence for ecological causation of sexual dimorphism in a hummingbird.

Unambiguous examples of ecological causes of animal sexual dimorphism are rare. Here we present evidence for ecological causation of sexual dimorphism in the bill morphology of a hummingbird, the purple-throated carib. This hummingbird is the sole pollinator of two Heliconia species whose flowers correspond to the bills of either males or females. Each sex feeds most quickly at the flower species approximating its bill dimensions, which supports the hypothesis that floral specialization has driven the evolution of bill dimorphism. Further evidence for ecological causation of sexual dimorphism was provided by a geographic replacement of one Heliconia species by the other and the subsequent development of a floral dimorphism, with one floral morph matching the bills of males and the other of females.

Animals↗
PubMed2003

In vitro antifungal activity of Micafungin (FK463) against dimorphic fungi: comparison of yeast-like and mycelial forms.

The characteristics of in vitro micafungin (FK463) antifungal activity against six species of dimorphic fungi were investigated in accordance with the NCCLS M27-A microdilution methods. MICs of micafungin, amphotericin B, itraconazole, and fluconazole for Histoplasma capsulatum var. capsulatum, Blastomyces dermatitidis, Paracoccidioides brasiliensis, Penicillium marneffei, and Sporothrix schenckii were determined both for the yeast-like form and mycelial form. Coccidioides immitis was tested only in its mycelial form. We have clearly demonstrated that the in vitro activity of micafungin depends considerably on the growth form of dimorphic fungi. Micafungin exhibited potent activity against the mycelial forms of H. capsulatum, B. dermatitidis, and C. immitis (MIC range, 0.0078 to 0.0625 micro g/ml), while it was very weakly active against their yeast-like forms (MIC range, 32 to >64 micro g/ml). Micafungin was also more active against the mycelial forms than the yeast-like forms of Paracoccidioides brasiliensis, Penicillium marneffei, and S. schenckii. The MICs of amphotericin B were 2 to 5 dilutions lower for the mycelial forms than for the yeast-like forms of B. dermatitidis and Paracoccidioides brasiliensis. There was no apparent difference in the activity of itraconazole between the two forms. The MICs of fluconazole for the yeast-like forms were generally lower than those for the mycelial forms, and considerably so for B. dermatitidis. These results suggest that the growth form employed in antifungal susceptibility testing of dimorphic fungi can considerably influence the interpretation of results. At present, it cannot be judged whether micafungin has clinical usefulness for dimorphic fungus infections, since for most fungi it remains uncertain which growth form correlates better with therapeutic outcome. However, the results of this study warrant further investigations of micafungin as a therapeutic agent for infections caused by dimorphic fungi.

Antifungal Agents↗
PubMed1977

Sexual dimorphism in metacarpal dimensions and body size of Mexican school children.

The hypothesis that patterns of sexual dimorphism in transverse dimensions of the metacarpal only reflect sex differences in body size was investigated in a sample of 324 Mexican school children 6.00-10.99 years of age. Several patterns of sexual dimorphism in second metacarpal dimensions are seen with regard to stature and weight. Sex differences in medullary diameter and percent cortical area are not related to sexual dimorphism in body size, while sex differences in cortical thickness are related to, but not fully explained by, differences in body size. Dimorphism in metacarpal diaphyseal diameter is related to differences in body size, but, at a constant body size and age, boys still have significantly larger diaphyseal diameters than girls. Finally, sexual dimorphism in cortical area is closely associated with sex differences in body size.

Age Factors↗
PubMed1982

Scaling of sexual dimorphism in body weight and canine size in primates.

Among primates sexual dimorphism in both body weight and canine size increases exponentially with increasing body size. This suggests that a full explanation of the variance in sexual dimorphism can only be attained if, in addition to sexual selection, parental investment, and various ecological factors, the influence of body size is taken into account. Positive allometry in both body weight dimorphism and canine size dimorphism is demonstrated to be associated with polygyny. In monogamous species the two dimorphisms not only remain constant throughout the size range but actually are minimal or lacking at any given body size.

Animals↗
PubMed2006

Sexual dimorphism, reproductive strategy, and human activities determine resource use by brown bears.

Despite significant sexual dimorphism and differing reproductive strategies in carnivores, sexual segregation is rarely studied and is often overlooked in the management of wild populations. Potential nutritional constraints imposed by sexual dimorphism and differing reproductive strategies between the sexes have important implications, particularly when combined with differential effects of human activities on sex and age classes. We examined the effects of sexual dimorphism, reproductive strategies, and human activities (bear-viewing and hunting) on resource use by different sex and age classes of brown bears (Ursus arctos). Sexual segregation of habitat use and effects of experimental bear-viewing were quantified at a single site in south-central Alaska, U.S.A., by capturing, collaring, and observing brown bears at a salt marsh and salmon stream. Effects of salmon capture rate, availability of alternative salmon runs, harvest pressure, and numbers of annual visitors on sex and age class use were examined from data collected or previously published from 13 other sites. Bear-viewing sites on salmon streams where salmon capture rates were low (<4 salmon/hour) resulted in low use by adult males (<10% of all bears), except for sites with falls. However, maximum male use of viewing areas also depended on the availability of alternative salmon streams and harvest pressure. Use of habitats by females with dependent young was significantly related to the prevalence of adult males at the site. Thus, both sexual dimorphism and differing reproductive strategies led to sexual segregation in habitat use by bears. As a result of infanticide, females with young appear to prioritize avoidance of male bears over avoidance of humans when choosing habitats, in contrast to responses documented in herbivores. Because carnivores often exhibit both sexual dimorphism and infanticide, selection for sexual segregation is likely to be high. In these cases, the nutritional demands of large adult males, balanced with responses to human activity, drive dynamic temporal and spatial distributions of individuals in the population.

Age Factors↗
PubMed2001

Viability, morphological characteristics and dimorphic ability of fungi preserved by different methods.

The viability, morphological characteristics and dimorphic ability of fungi were evaluated. Strain subcultures were maintained under mineral oil and in soil for different periods of time, ranging from 49 to eight years. Of the 16 Blastomyces dermatitidis strains, four maintained viability and were able to complete the dimorphic process to the M phase producing a large amount of conidia, but were unable to form Y cells at 36 degrees C. Of the 15 Histoplasma capsulatum var. capsulatum strains, only one was viable but it was impossible to check its identity because it lost sporulating and dimorphic ability. Of the 53 Sporothrix schenckii strains, 37 were viable, 28 able to sporulate and 12 of them completed the whole M <=> Y dimorphic process. All subcultures in soil became inviable. The results demonstrate that the preservation methods used here affected the morphology and sporulating and dimorphic ability of the strains. B. dermatitidis and S. schenckii were considered to be species that survive better than H. capsulatum var. capsulatum under mineral oil. Thus, it is necessary to establish routine monitoring and appropriate environmental and culture conditions, using less widely spaced transplants and choosing the exact time of intervention to induce growth and development restriction in each strain.

Journal Article↗
PubMed2006

Patterns of sexual dimorphism from birth to senescence.

Sexual dimorphism is expressed as median of the female values in percent of the median of the male values, of 4 length measurements, 3 circumferences, and 5 measurements of corpulence respectively fat. Data were obtained from a cross-sectional sample of more than 41.000 German subjects, aged from birth to age 62. The pattern of sexual dimorphism is similar in the length measurements. Girls are shorter at birth, but they increase in length at higher rates than boys and even temporarily overgrow the boys up to age 12. Thereafter, males show an obvious growth advantage leading to some 6 to 9% more length in adult males. In contrast, female circumferences are always smaller, from birth to senescence. Though, the differences between the sexes are low in circumferences, up to age 13, sexual dimorphism increases to 17% in the thoracic circumference at adulthood. Sexual dimorphism in weight and BMI is comparably with that in length measurements while subcutaneous fat and total body fat content are always higher in females. The results highlight that sexual dimorphism develops at different pace in the various components of the body and that it associates with a sex specific growth tempo.

Adolescent↗