Structural organization, chromosomal localization, expression and phylogenetic evaluation of mouse glutathione peroxidase encoding genes

National audienceWe have reported earlier the cloning and the chromosomal localization of 2 GPX-encoding sequences expressed differentially within the mouse epididymis, gpx5 and gpx3. Here, we have mapped on the mouse chromosomes the third known murine GPX-encoding gene, the cytosolic GPX or gpx1. We have compared the degree of identity of the 3 GPX proteins, the respective organization of the 3 corresponding single copy genes and, using degenerated oligonucleotides designed in highly conserved domains of the proteins, we have analyzed the expression of GPX-encoding genes in the mouse epididymis as well as in control tissues known to express GPX proteins (the liver for GPX1 and the kidney for GPX3). The 3 genes characterized to date were found expressed in each of the tissues tested but in a highly tissue-restricted manner. Nucleotidic sequences comparisons were carried out on GPX-encoding sequences from various species and were used to draw a dendrogram. Phylogenetic evaluation of the sequence information, as well as the chromosomal localizations, suggest that the GPX genes have evolved by duplication events followed by random insertions from a single ancestral gene

Characterization of an androgen response element within the promoter of the epididymis-specific murine glutathione peroxidase 5 gene

International audienceWe have shown in earlier studies, using a mouse model, that the expression of the glutathione peroxidase 5 protein (GPX5) is restricted to the epididymis and that the accumulation of its corresponding mRNA is hormonally, spatially and temporally regulated throughout postnatal development. We report here, using run-on assays, transient expression experiments as well as gel-shift and footprinting analyses on the findings that at least part of the androgenic control of the GPX5 expression is exerted at the transcriptional level via an androgen response element localized in the distal promoter region of the GPX5 gene. The gpx5 androgen response element (ARE) is found to be consistent with the consensus palindromic steroid-receptor target sequence 5'-AGWACWnnnTGTYCT-3' but exhibits a quite weak conservation in the left half site. The data presented here further expand the diversity of sequence able to confer androgen responsiveness

Structural organization, chromosomal localization, expression and phylogenetic evaluation of mouse glutathione peroxidase encoding genes

National audienceWe have reported earlier the cloning and the chromosomal localization of 2 GPX-encoding sequences expressed differentially within the mouse epididymis, gpx5 and gpx3. Here, we have mapped on the mouse chromosomes the third known murine GPX-encoding gene, the cytosolic GPX or gpx1. We have compared the degree of identity of the 3 GPX proteins, the respective organization of the 3 corresponding single copy genes and, using degenerated oligonucleotides designed in highly conserved domains of the proteins, we have analyzed the expression of GPX-encoding genes in the mouse epididymis as well as in control tissues known to express GPX proteins (the liver for GPX1 and the kidney for GPX3). The 3 genes characterized to date were found expressed in each of the tissues tested but in a highly tissue-restricted manner. Nucleotidic sequences comparisons were carried out on GPX-encoding sequences from various species and were used to draw a dendrogram. Phylogenetic evaluation of the sequence information, as well as the chromosomal localizations, suggest that the GPX genes have evolved by duplication events followed by random insertions from a single ancestral gene

Characterization of an androgen response element within the promoter of the epididymis-specific murine glutathione peroxidase 5 gene

International audienceWe have shown in earlier studies, using a mouse model, that the expression of the glutathione peroxidase 5 protein (GPX5) is restricted to the epididymis and that the accumulation of its corresponding mRNA is hormonally, spatially and temporally regulated throughout postnatal development. We report here, using run-on assays, transient expression experiments as well as gel-shift and footprinting analyses on the findings that at least part of the androgenic control of the GPX5 expression is exerted at the transcriptional level via an androgen response element localized in the distal promoter region of the GPX5 gene. The gpx5 androgen response element (ARE) is found to be consistent with the consensus palindromic steroid-receptor target sequence 5'-AGWACWnnnTGTYCT-3' but exhibits a quite weak conservation in the left half site. The data presented here further expand the diversity of sequence able to confer androgen responsiveness

Selenium-independent epididymis-restricted glutathione peroxidase 5 protein (GPX5) can back up failing Se-dependent GPXs in mice subjected to selenium deficiency.

International audienceWe have previously characterized and cloned a secreted sperm-bound selenium-independent glutathione peroxidase protein (GPX5), the expression of which was found to be restricted to the mouse caput epididymidis. Because of the lack of selenium (Se) in the active site of this enzyme, unlike the other animal GPXs characterized to date, it was suspected that GPX5 does not function in the epididymis as a true glutathione peroxidase in vivo. In the present report, following dietary selenium deprivation which is known to reduce antioxidant defenses and favor oxidative stress in relation with depressed Se-dependent GPX activities, we show that the epididymis is still efficiently protected against increasing peroxidative conditions. In this model, the caput epididymides of selenium-deficient animals showed a limited production of lipid peroxides, a total GPX activity which was not dramatically affected by the shortage in selenium availability and an increase in GPX5 mRNA and protein levels. Altogether, these data strongly suggest that the selenium-independent GPX5 could function as a back-up system for Se-dependent GPXs

Thermally induced torpor in fullterm lizard embryos synchronizes hatching with ambient conditions

Eggs inside an underground nest have limited access to information about above-ground conditions that might affect the survival of emerging hatchlings. Our measurements of heart rates of embryos inside the intact eggs of montane lizards (Bassiana duperreyi, Scincidae) show that low temperatures induce torpor in fullterm embryos, but do not do so during earlier embryogenesis or later, post-hatching. Because above-ground conditions affect soil temperatures, this stage-dependent torpor effectively restricts hatching to periods of high ambient temperatures above ground. Torpor thus can function not only to synchronize activity with suitable environmental conditions during post-hatching life (as reported for many species), but also can occur in embryos, to synchronize hatching with above-ground conditions that facilitate successful emergence from the nest

Reproductive modes in lizards: measuring fitness consequences of the duration of uterine retention of eggs

1. One of the primary axes of life-history variation involves the proportion of embryonic development for which the offspring is retained within its parent's body; understanding trade-offs associated with prolonging that period thus is a critical challenge for evolutionary ecology.\ud \ud 2. Prior to oviposition, most oviparous squamate reptiles retain developing eggs in utero for about one-third of embryogenesis; the strong conservatism in this trait is a major puzzle in reptilian reproduction. To clarify fitness consequences of this prolonged uterine retention, we need to experimentally modify the trait and examine the effects of our manipulation.\ud \ud 3. We used transdermal application of corticosterone to induce gravid scincid lizards (Bassiana duperreyi) to lay their eggs 'prematurely', with relatively undeveloped embryos. Corticosterone application induced females to oviposit sooner (mean of 5.41 ± 0.51 days post-treatment) at earlier embryonic developmental stage (27 ± 0.21) than did controls (13.2 ± 1.22 days; embryonic stage 30.4 ± 0.16).\ud \ud 4. Corticosterone levels in the egg yolk were unaffected by maternal treatment, so effects of earlier oviposition should not be confounded by endocrine disruption of embryogenesis. Nonetheless, early oviposition reduced hatchling fitness. Hatching success was lower, incubation periods post-laying were increased, and neonates from eggs laid at earlier embryonic stages were smaller and slower.\ud \ud 5. These results suggest that retention of developing eggs in utero by oviparous squamates enhances maternal fitness, and does so via modifications to offspring phenotypes rather than (for example) due to accelerated developmental rates of eggs in utero compared to in the nest.\ud \ud 6. More generally, our data support optimality models that interpret interspecific variation in the duration of maternal–offspring contact in terms of the selective forces that result from earlier vs. later termination of that maternal investment

Consequences of maternal yolk testosterone for offspring development and survival : experimental test in a lizard

1. Hormone-mediated maternal effects and developmental plasticity are important sources of phenotypic variation, with potential consequences for trait evolution. Yet our understanding of the importance of maternal hormones for offspring fitness in natural populations is very limited, particularly in non-avian species.2. We experimentally elevated yolk testosterone by injection of a physiological dose into eggs of the lizard Ctenophorus fordi Storr, to investigate its roles in offspring development, growth and survival.3. Yolk testosterone did not influence incubation period, basic hatchling morphology or survival under natural conditions. However, there was evidence for increased growth in hatchlings from testosterone-treated eggs, suggesting that maternal hormones have potential fitness consequences in natural populations.4. The positive effect of prenatal testosterone exposure on postnatal growth could represent a taxonomically widespread developmental mechanism that has evolved into an adaptive maternal effect in some taxa, but remains deleterious or selectively neutral in others.5. A broader taxonomic perspective should increase our understanding of the role of physiological constraints in the evolution of endocrine maternal effects.<br /

Ecology of Mabuya agilis (Raddi) (Lacertilia, Scincidae) at the restinga of Grumari, Rio de Janeiro, southeastern Brazil

Some aspects of the ecology of the skink Mabuya agilis (Raddi, 1823) at the restinga habitat of Grumari, in Rio de Janeiro, Brazil are studied. Most of the lizards were first sighted on the ground, though a few were using perches (mainly cacti) up to 30 cm high. Mean body temperature in activity was 33.1 ± 2.4ºC and was significantly correlated to air temperature. There was sexual dimorphism in size (snout-vent length - SVL), with females growing larger than males. Frequency of broken tails was high overall (83%) and did not differ between sexes. Females and males are sexually mature at 49 mm and 47 mm SVL, respectively. Brood size averaged 3.2 ± 1.0 (range 1-5) and was positively and significantly related to female SVL (r = 0.65, p = 0.001). Relative clutch mass (RCM) of seven gravid females averaged 0.250 ± 0.042, being relatively low compared to those of other congeners. The diet of M. agilis was composed basically of arthropods, with relatively large and soft-bodied arthropods such as spiders, caterpillars and homopterans being the most important prey. The results of our work confirm and expand the knowledge of ecological tendencies previously observed for M. agilis in other areas