Dose-response relations for dicentric yields in G0 lymphocytes on man and crab-eating monkey following acute and chronic γ-irradiations

A comparison has been made of dicentric yields in G₀ lymphocytes between man and crab-eating monkey, Macaca fascicularis, after acute and chronic γ-irradiations. With acute irradiation (49.6 rad/min) there was no significant difference between them, but for the chronic irradiation (17.1 rad/h) a significant difference was observed between the species. When the dose-response relations were fitted to the linear-quadratic model (Y = αD + βD²), the species-difference observed for chronic irradiation was almost entirely due to change in the value of β. In addition, after chronic irradiation the β-value for monkey was almost negligible, but that for man was significant. Post-irradiation incubation experiment showed that cells with dicentrics were partly eliminated during the course of chronic irradiation, because there were appreciable reductions of dicentric yields (ca. 25% for both man and monkey at 400 rad) together with mitotic indices (ca. 30% and 60% for man and monkey, respectively, at 400 rad). Accordingly, it would be reasonable to postulate that G₀ repair for dicentrics other than selection mechanism must play a major role in the effects of low dose rate. It can be further suggested that G₀-repair capacity for chromosal damages leading to dicentrics may be different among different primate species.     

Dicentric yields induced by gamma-radiation and chromosome arm number in primates.

To evaluate the effect of the chromosome arm number on the yield of dicentric chromosomes, frequencies of gamma-ray-induced chromosome aberrations were examined with peripheral lymphocytes from three different primate species, Saimiri sciureus (arm number, 77), Macaca fascicularis (arm number, 83) and Nycticebus coucang (arm number, 99). Irradiated blood samples were cultured by the same standard technique as that commonly used for human lymphocytes. The yields of dicentrics and dicentrics plus rings at doses of 100, 200 and 300 rad of gamma-irradiation were not significantly different among the three species, in spite of the difference in the chromosome arm number. Furthermore, dose-response relationships for these species were consistent with that for man. Statistical analysis indicated that the expected dicentric yields calculated from the arm number model were significantly different from the observed yields at 200 and 300 rad doses (P less than 0.01). From these results it can be pointed out that there is no correlation between the yield of dicentrics and the effective chromosome arm number, and that the chromosomal radiosensitivity of these primates is essentially the same as that of man, at least in the lymphocyte system.     

Aberrations induced by fission neutrons in human peripheral lymphocytes

Analysis of dose-response relationship was carried out for chromosome aberrations produced in human peripheral lymphocytes by fission neutrons at doses of 25, 50, 100 or 200 rad.Statistical treatment showed experimental data to be fitted by a regression curve described by the mathematical model Y = a+bD. A linear relation to dose characterized both one-break and two-break aberration yields. Numerical values of coefficients are reported for yields of dicentrics, chromosome fragments, minutes, aberrant cells, total number of aberrations, and total breakage.Based on chromosome fragments and aberrant cells, relative biological efficiency (RBE) value derived for fission neutrons relative to 180 kV X-rays for chromosome fragments was 2.53, and for aberrant cells it was 2.80.     

The relative radiosensitivities of human,rabbit and rat-kangaroo chromosomes

Lymphocytes of man, rabbit and potoroo (Potorous tridactylus) were exposed, in vitro, to various doses of X-rays and analysed at their first mitotic division for chromosome structural abnormalities. The ratio of yields of dicentric aberrations in the three species was, respectively, 1.00∶0.46∶0.29 and of deletions 1.00∶0.62∶1.13. Similar results were obtained for human and rabbit cells exposed to fast neutrons. — In lymphocytes of six mammalian species, including man, Brewen et al. (1973) found a linear relationship between chromosome arm number and relative dicentric frequencies. Our data for potoroo cells (24 chromosome arms) fit in well with this linear response but our rabbit data do not: on the basis of chromosome arm number the dicentric frequency in rabbit (80 arms) should be similar to that for man (81 arms) whereas dicentrics are less than half as frequent in rabbit cells. — The differences in DNA content (man:rabbit, 1.00∶0.92) and lymphocyte nuclear volumes (1.00∶0.84) are too small to explain the differential dicentrie frequencies. It is suggested that the capacity for accurate DNA repair may differ between species and be reflected in different frequencies of chromosome exchange.     

Implementation of a dose–response curve for γ-radiation in the Portuguese population by use of the chromosomal aberration assay

An in vitro dose–response curve following exposure to γ-radiation was determined at the IST/ITN, by use of the chromosomal aberration assay. This is the first study of this kind carried out among the Portuguese population. Un-irradiated and γ-irradiated peripheral blood lymphocytes from 16 healthy donors were cultured. A total of 22,395 metaphases were analyzed for frequency and distribution of dicentrics and centric rings, as a function of the radiation dose. The dose–response data for dicentrics and dicentrics plus centric rings were fitted by use of a linear–quadratic model: Y_dic = (0.0011 ± 0.0006) + (0.0105 ± 0.0035)D + (0.0480 ± 0.0019)D² and Y_{dic + rings} = (0.0011 ± 0.0006) + (0.0095 ± 0.0036)D + (0.0536 ± 0.0020)D². Also, calibration curves related to age and gender were determined, but no significant differences were found. Following the establishment of the dose–response curves, a validation experiment was carried out with three individuals. Real and estimated doses, obtained with the dose–response curves, were in agreement. These results give us confidence to apply both dose–response calibration curves in future biological dosimetry requirements.     

Kinetics of Growth and Amylase Production of Saccharomycopsis fibuligera on Potato Processing Wastewater

The kinetics of growth and amylase production of Saccharomycopsis fibuligera were studied in a chemostat on a synthetic potato processing blancher water. Dilution rates (D) from 0.101 to 0.480 h⁻¹ were examined. A mathematical model based on the Monod equation was developed. The yield of cell mass from carbohydrates was constant and equal to 0.84. The maximum specific growth rate and the Monod constant were determined to be 0.596 h⁻¹ and 0.226 mg/ml, respectively. An equation for the steady-state starch concentrations was empirically derived. The steady-state noncarbohydrate carbon levels rose linearly with D. Reducing sugars were the growth-limiting substrate, and their steady-state levels conformed to Monod kinetics. The yield of amylase from the cell mass (Y_z) declined as D rose and was described by the equation Y_z = (−8.005D + 4.076). The model predicted that the maximum production of cell mass should occur at D = 0.35 h⁻¹ and the maximum production of amylase should occur at D = 0.22 h⁻¹. The mathematical model presented agreed with the experimental results in its prediction of the steady-state level of reducing sugar, starch, cell mass, and amylase concentrations as well as the productivity of amylase.     

X-Y Exchange and the Coevolution of the X and Y Rdna Arrays in Drosophila melanogaster

The nucleolus organizers on the X and Y chromosomes of Drosophila melanogaster are the sites of 200-250 tandemly repeated genes for ribosomal RNA. As there is no meiotic crossing over in male Drosophila, the X and Y chromosomal rDNA arrays should be evolutionarily independent, and therefore divergent. The rRNAs produced by X and Y are, however, very similar, if not identical. Molecular, genetic and cytological analyses of a series of X chromosome rDNA deletions (bb alleles) showed that they arose by unequal exchange through the nucleolus organizers of the X and Y chromosomes. Three separate exchange events generated compound X·Y ^L chromosomes carrying mainly Y-specific rDNA. This led to the hypothesis that X-Y exchange is responsible for the coevolution of X and Y chromosomal rDNA. We have tested and confirmed several of the predictions of this hypothesis: First, X· Y^L chromosomes must be found in wild populations. We have found such a chromosome. Second, the X·Y^L chromosome must lose the Y^L arm, and/or be at a selective disadvantage to normal X⁺ chromosomes, to retain the normal morphology of the X chromosome. Six of seventeen sublines founded from homozygous X·Y^Lbb stocks have become fixed for chromosomes with spontaneous loss of part or all of the appended Y^L. Third, rDNA variants on the X chromosome are expected to be clustered within the X⁺ nucleolus organizer, recently donated (" Y") forms being proximal, and X-specific forms distal. We present evidence for clustering of rRNA genes containing Type 1 insertions. Consequently, X-Y exchange is probably responsible for the coevolution of X and Y rDNA arrays.     

Effect of immobilized laminin on karyotypic variability in two karyotypically different variants of the indian muntjac skin fibroblast cell line

The numerical and structural karyotypic variability has been investigated in MTs of the markerless cell line of Indian muntjac skin fibroblasts, as well as in its karyotypic variant MT^D cultivated on a laminin 2/4 coated surface. In the MT cell line preincubated in serum-free medium for 2.5 and 1.0 h, then cultivated on a laminin-coated surface in serum-containing medium for one, two, and three days, the character of cell distribution for the chromosome number has changed. These changes involve a significant decrease in the frequency of cells with modal numbers of chromosomes and an increase in frequency of cells with lower chromosome numbers. Some new additional structural variants of the karyotype (SVK) appeared. The observed alterations seem to be due to disturbances of the chromosome segregation and the establishment of a new advantageous balanced karyotypic structure. In the karyotypic variant MT^D differing from MT by an increased number of dicentrics (telomeric associations) cultivated under the same conditions, the character of cell distribution for the chromosome number did not change. In the MT cell line, the frequency of chromosomal aberrations did not change relative to control variants. In the karyotypic variant MT^D under the same conditions, the frequency of chromosomal aberrations significantly increased after three days mainly due to the formation of dicentrics. These results confirm the conclusion that, like aneuploidy, the formation of dicentrics in markerless cell lines appears to be the way in which the cell population adapts to unfavorable environmental factors. Possible reasons for differences in the character of the numerical and structural karyotypic variability between the MT cell line and its karyotypic variant MT^D are discussed.     

Genetic dissection of testis weight in mice: quantitative trait locus analysis using F2 intercrosses between strains with extreme testis weight, and association study using Y-consomic strains

In the present study, dissection of genetic bases of testis weight in mice was performed. Autosomes and the X chromosome were searched using traditional quantitative trait locus (QTL) scans, and the Y chromosome was searched by association studies of Y-consomic strains. QTL analysis was performed in ??DDD?×???CBA F₂ mice; the inbred mouse DDD has the heaviest testes, whereas the inbred mouse CBA has the lightest testes. Two significant testis weight QTLs were identified on chromosomes 1 and X. A DDD allele was associated with increased and decreased testis weight at the locus on chromosomes 1 and X, respectively. In the reciprocal cross ??CBA?×???DDD F₂ mice, QTL on chromosome 1, and not on chromosome X, had a significant effect on testis weight. The DDD allele at the X-linked locus could not sustain testis weight in combination with the Y chromosome of the CBA strain. The Y chromosome per se had a significant effect on testis weight, i.e., DH-Chr Y^DDD had significantly heavier testes than DH-Chr Y^CBA. On the basis of the results of Y-chromosome-wide association studies using 17 Y-consomic strains, variations in Uty, Usp9y, and Sry were significantly associated with testis weight. Thus, testis weight is a complex quantitative phenotype controlled by multiple genes on autosomes and sex chromosomes and their interactions.     

Origin of the X1X1X2X2/X1X2Y sex chromosome system of Harttia punctata (Siluriformes,Loricariidae) inferred from chromosome painting and FISH with ribosomal DNA markers

Harttia is a genus in the subfamily Loricariinae that accommodates fishes popularly known as armored catfishes. They show extensive karyotypic diversity regarding interspecific numerical/structural variation of the karyotypes, with the presence of the XX/XY₁Y₂ multiple sex chromosome system, as found in H. carvalhoi. In this context, this study aimed to characterize Harttia punctata chromosomally, for the first time, and to infer the rearrangements that originated the X₁X₁X₂X₂/X₁X₂Y multiple sex chromosome system present in this species. The data obtained in this study, with classical (Giemsa, C-banding and AgNORs) and molecular methodologies (fluorescence in situ hybridization) and chromosome microdissection, indicated that a translocation between distinct acrocentric chromosomes bearing rRNA genes, accompanied by deletions in both chromosomes, might have originated the neo-Y chromosome in this species. The data also suggest that the multiple sex chromosome systems present in H. carvalhoi and H. punctata had an independent origin, evidencing the recurrence of chromosome alterations in species from this genus.     

Synaptonemal complex of the sex-autosome trivalent in a male Indian muntjac

Bright-field microscopy of silver-stained pachytene spermatocytes of a male Indian muntjac, Muntiacus muntjak revealed that (a) the synapsis between the autosomal homologs, including the long arm of the X and Y₂, was normal, (b) the nucleolus organizer regions were present in both the No. 1 bivalent and the long arm of the X and Y₂, (c) the accessory structures of the X chromosome short arm in the forms of light and dark thickenings and the hairpin-like bend were present despite the X-autosome translocation, (d) a short synaptonemal complex was present between the Y₁ (real Y) and the short arm of the X chromosome, and (e) the centromeric orientation of the Y₁ and Y₂ chromosomes was in Cis configuration as opposed to the X chromosome.     

Sexual differentiation in the developing mouse brain: contributions of sex chromosome genes

Neural sexual differentiation begins during embryogenesis and continues after birth for a variable amount of time depending on the species and brain region. Because gonadal hormones were the first factors identified in neural sexual differentiation, their role in this process has eclipsed investigation of other factors. Here, we use a mouse with a spontaneous translocation that produces four different unique sets of sex chromosomes. Each genotype has one normal X‐chromosome and a unique second sex chromosome creating the following genotypes: XY^*x, XX, XY^*, XX^Y*. This Y^* mouse line is used by several laboratories to study two human aneuploid conditions: Turner and Klinefelter syndromes. As sex chromosome number affects behavior and brain morphology, we surveyed brain gene expression at embryonic days 11.5 and 18.5 to isolate X‐chromosome dose effects in the developing brain as possible mechanistic changes underlying the phenotypes. We compared gene expression differences between gonadal males and females as well as individuals with one vs. two X‐chromosomes. We present data showing, in addition to genes reported to escape X‐inactivation, a number of autosomal genes are differentially expressed between the sexes and in mice with different numbers of X‐chromosomes. Based on our results, we can now identify the genes present in the region around the chromosomal break point that produces the Y^* model. Our results also indicate an interaction between gonadal development and sex chromosome number that could further elucidate the role of sex chromosome genes and hormones in the sexual differentiation of behavior.     

Model of yield response of corn to plant population and absorption of solar energy

Biomass yield of agronomic crops is influenced by a number of factors, including crop species, soil type, applied nutrients, water availability, and plant population. This article is focused on dependence of biomass yield (Mg ha⁻¹ and g plant⁻¹) on plant population (plants m⁻²). Analysis includes data from the literature for three independent studies with the warm-season annual corn (Zea mays L.) grown in the United States. Data are analyzed with a simple exponential mathematical model which contains two parameters, viz. Y_m (Mg ha⁻¹) for maximum yield at high plant population and c (m² plant⁻¹) for the population response coefficient. This analysis leads to a new parameter called characteristic plant population, x_c = 1/c (plants m⁻²). The model is shown to describe the data rather well for the three field studies. In one study measurements were made of solar radiation at different positions in the plant canopy. The coefficient of absorption of solar energy was assumed to be the same as c and provided a physical basis for the exponential model. The three studies showed no definitive peak in yield with plant population, but generally exhibited asymptotic approach to maximum yield with increased plant population. Values of x_c were very similar for the three field studies with the same crop species.     

Genetic factors affecting normal growth of testes inDrosophila hydei

Summary A marked growth in the length of testes ofDrosophila hydei males occurred during pupal development. This growth continued over the first 8 days of adult life and in the young adults sperm were not produced until the testes increased approximately threefold in length to about 28 mm. The length of testes is correlated with genetic factors on the X and Y chromosomes. In males lacking a Y chromosome (X/O) or the short arm (Y^S) of the Y chromosome (X/Y^L) the testes were about half the length of testes of control males (X/Y) or double Y males (X/Y/Y). Males with deletions of the distal Y^L chromosome arm had testicular lengths equivalent to the controls. Males with short testes (X/O and X/Y^L) showed disruptions to spermatogenesis at meiosis and an absence of normal spermatid elongation. Reduction of active ribosomal RNA genes on the X chromosome in X/O caused an increased expression ofbobbed (bb) and a corresponding reduction in length of testes. Severelybobbed X/O males had very few cysts of spermatogonia and these cysts did not develop into primary spermatocytes.     

Sex Chromosome Translocations in the Evolution of Reproductive Isolation

Haldane's rule states that in organisms with differentiated sex chromosomes, hybrid sterility or inviability is generally expressed more frequently in the heterogametic sex. This observation has been variously explained as due to either genic or chromosomal imbalance. The fixation probabilities and mean times to fixation of sex-chromosome translocations of the type necessary to explain Haldane's rule on the basis of chromosomal imbalance have been estimated in small populations of Drosophila melanogaster. The fixation probability of an X chromosome carrying the long arm of the Y(X·Y^L) is approximately 30% greater than expected under the assumption of no selection. No fitness differences associated with the attached Y^L segment were detected. The fixation probability of a deficient Y chromosome is 300% greater than expected when the X chromosome contains the deleted portion of the Y. It is suggested that sex-chromosome translocations may play a role in the establishment of reproductive isolation.     

The influence of DNA content and nuclear volume on the frequency of radiation-induced chromosome aberrations in Bufo species

The frequency of chromosome aberrations was compared in X-irradiated blood lymphocytes of Bufo marinus, B. calamita and B. pardalis which have similar chromosome numbers (2n=22) and karyotypes but differ in chromosomal DNA content and nuclear volume. — For each species the yield, per cell of centric exchange aberrations (dicentrics+rings) and of deletions (interstitial and terminal) increased approximately as the 1.5th power of the dose. — The 55% higher chromosomal DNA content of B. pardalis compared with both B. marinus and B. calamita resulted in the same increase in the frequency of deletions as a 55% increase in radiation dose, approximately doubling the yield. Both factors probably lead to a similar increase in the frequency of primary lesions from which the deletions are derived. — In contrast, an increase in chromosomal DNA content did not result in a higher yield of dicentric and ring exchanges, probably because the greater nuclear volume of B. pardalis (twice that of the other species) offset the potential increase in exchanges by increasing the average distance between chromosomes and chromosome arms. The data support the hypothesis that, in order to be involved in exchange, chromosome regions must be close together at the time of irradiation. The frequency of deletions is unaffected by changes in nuclear volume.     

The platelet P2Y12 receptor under normal and pathological conditions. Assessment with the radiolabeled selective antagonist [3H]PSB-0413

Various radioligands have been used to characterize and quantify the platelet P2Y₁₂ receptor, which share several weaknesses: (a) they are metabolically unstable and substrates for ectoenzymes, (b) they are agonists, and (c) they do not discriminate between P2Y₁ and P2Y₁₂. We used the [³H]PSB-0413 selective P2Y₁₂ receptor antagonist radioligand to reevaluate the number of P2Y₁₂ receptors in intact platelets and in membrane preparations. Studies in humans showed that: (1) [³H]PSB-0413 bound to 425 ± 50 sites/platelet (K_D = 3.3 ± 0.6 nM), (2) 0.5 ± 0.2 pmol [³H]PSB-0413 bound to 1 mg protein of platelet membranes (K_D = 6.5 ± 3.6 nM), and (3) competition studies confirmed the known features of P2Y₁₂, with the expected rank order of potency: AR-C69931MX > 2MeSADP ≫ ADPβS > ADP, while the P2Y₁ ligand MRS2179 and the P2X₁ ligand α,β-Met-ATP did not displace [³H]PSB-0413 binding. Patients with severe P2Y₁₂ deficiency displayed virtually no binding of [³H]PSB-0413 to intact platelets, while a patient with a dysfunctional P2Y₁₂ receptor had normal binding. Studies in mice showed that: (1) [³H]PSB-0413 bound to 634 ± 87 sites/platelet (K_D = 14 ± 4.5 nM) and (2) 0.7 pmol ± 0.3 [³H]PSB-0413 bound to 1 mg protein of platelet membranes (K_D = 9.1 ± 5.3 nM). Clopidogrel and other thiol reagents like pCMBS or DTT abolished the binding both to intact platelets and membrane preparations. Therefore, [³H]PSB-0413 is an accurate and selective tool for radioligand binding studies aimed at quantifying P2Y₁₂ receptors, to identify patients with P2Y₁₂ deficiencies or quantify the effect of P2Y₁₂ targeting drugs.     

Experimental and simulated light responses of photosynthesis in leaves of three tree species under different soil water conditions

Water deficit is one of the major limiting factors in vegetation recovery and restoration in loess, hilly-gully regions of China. The light responses of photosynthesis in leaves of two-year old Prunus sibirica L., Hippophae rhamnoides L., and Pinus tabulaeformis Carr. under various soil water contents were studied using the CIRAS-2 portable photosynthesis system. Light-response curves and photosynthetic parameters were analyzed and fitted using the rectangular hyperbola model, the exponential model, the nonrectangular hyperbola model, and the modified rectangular hyperbola model. Under high light, photosynthetic rate (P _N) and stomatal conductance (g _s) were steady and photoinhibition was not significant, when the relative soil water content (RWC) varied from 56.3–80.9%, 47.9–82.9%, and 33.4–92.6% for P. sibirica, H. rhamnoides, and P. tabulaeformis, respectively. The light-response curves of P _N, the light compensation point (LCP), and the dark respiration rate (R _D) were well fitted using the above four models. The nonrectangular hyperbola was the best model in fitting the data; the modified rectangular hyperbola model was the second, and the rectangular hyperbola model was the poorest one. When RWC was higher or lower than the optimal range, the obvious photoinhibition and significant decrease in P _N with increasing photosynthetic photon flux density (PPFD) were observed in all three species under high light. The light saturation point (LSP) and apparent quantum yield also decreased significantly, when the upper limit of PPFD was 200 μmol m^?2 s^?1. Under these circumstances, only the modified rectangular hyperbola model was able to fit well the curves of the light response, LCP, LSP, R _D, and light-saturated P _N.     

A probability distribution model of small -scale species richness in plant communities

We devised a probability distribution model that best expressed species richness per quadrat in grassland communities, and clarified the mechanism by which the mean richness per quadrat was always larger than the variance among quadrats. Our model will aid in the understanding of community structures, and allow comparisons among different communities. The model was constructed based on relatively simple theoretical assumptions about the mechanisms in play in target communities. We assumed in the model that the number of species occurring in an actual quadrat, j, is the sum of “the fundamental number of species”, k (constant), and “a fluctuating number of species”, i (a Poisson variate with the mean of μ); that is, j = k + i, where i, j and k are non-negative integers. The probability that j species occur in a quadrat is given by a Poisson-like distribution (extended Poisson), with two parameters k and μ. The mean species richness in the probability distribution is expressed by λ (= k + μ), and the variance is λ − k. The proposed model afforded a good fit for the observed frequency distribution of species richness per quadrat. If even one species is common among many quadrats, the mean number of species per quadrat is greater than the variance. The greater the number of common species among quadrats is, the larger is the value of k, and then the more pronounced is the difference between the mean and the variance (although the variance does not change). We fitted the model to 55 datasets collected by ourselves from grasslands in various locations (Tibet, Inner Mongolia, Slovakia, or Japan), with varying quadrat size (0.25, 0.0625, or 0.01 m²), and under differing management status (various stocking densities).