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At least 109 records · Page 6Linked to original sources
PubMed2001

The genetics of reproductive isolation and the potential for gene exchange between Drosophila pseudoobscura and D. persimilis via backcross hybrid males.

Hybrid male sterility, hybrid inviability, sexual isolation, and a hybrid male courtship dysfunction reproductively isolate Drosophila pseudoobscura and D. persimilis. Previous studies of the genetic bases of these isolating mechanisms have yielded only limited information about how much and what areas of the genome are susceptible to interspecies introgression. We have examined the genetic basis of these barriers to gene exchange in several thousand backcross hybrid male progeny of these species using 14 codominant molecular genetic markers spanning the five chromosomes of these species, focusing particularly on the autosomes. Hybrid male sterility, hybrid inviability, and the hybrid male courtship dysfunction were all associated with X-autosome interactions involving primarily the inverted regions on the left arm of the X-chromosome and the center of the second chromosome. Sexual isolation from D. pseudoobscura females was primarily associated with the left arm of the X-chromosome, although both the right arm and the center of the second chromosome also contributed to it. Sexual isolation from D. persimilis females was primarily associated with the second chromosome. The absence of isolating mechanisms being associated with many autosomal regions, including some large inverted regions that separate the strains, suggests that these phenotypes may not be caused by genes spread throughout the genome. We suggest that gene flow between these species via hybrid males may be possible at loci spread across much of the autosomes.

Alleles↗
PubMed1989

On the origin of meiotic reproduction: a genetic modifier model.

We study the conditions under which a rare allele that modifies the relative rates of meiotic reproduction and apomixis increases in a population in which meiotic reproduction entails selfing as well as random outcrossing. A distinct locus, at which mutation maintains alleles that are lethal in homozygous form, determines viability. We find that low viability of carriers of the lethal alleles, high rates of selfing, dominance of the introduced modifier allele, and lower rates of recombination promote the evolution of meiosis. Meiotic reproduction can evolve even in the absence of linkage between the modifier and the viability locus. The adaptive value of meiotic reproduction depends on the relative viabilities of offspring derived by meiosis and by apomixis, and on associations between the modifier and the viability locus. Meiotic reproduction, particularly under selfing, generates more diverse offspring, including those with very high and very low viability. Elimination of offspring with low viability generates positive associations between enhancers of meiotic reproduction and high viability. In addition, partial selfing generates positive associations in heterozygosity (identity disequilibrium) between the modifier and the viability locus, even in the absence of linkage. The two kinds of associations together can compensate for initial reductions in mean offspring viability under meiotic reproduction.

Biological Evolution↗
PubMed2005

Evolutionary genetics of reproductive behavior in Drosophila: connecting the dots.

Species of the genus Drosophila exhibit enormous variation in all of their reproductive behaviors: resource use and specialization, courtship signaling, sperm utilization, and female remating. The genetic bases of this variability and its evolution are poorly understood. At the same time, Drosophila comparative genomics now has developed to a point at which approaches previously only possible with D. melanogaster can be exploited to address these questions. We have taken advantage of the known phylogenetic relationships of this group of flies not only to place these behaviors in an evolutionary framework, but to provide a roadmap for future genetic studies.

Animals↗
PubMed2004

[Multicolor fluorescence in situ hybridization and its application in genetic toxicology].

Multicolor fluorescence in situ hybridization, a new promising technology today, offers unparalleled capabilities for detection of nucleic acid sequences, chromosomes and genes. Owing to structural and numerical chromosomal aberrations were considered as important biological end points in genotoxic studies, chromosomal aberrations after exposure to occupational, medical, and environmental toxicants could be accurately and appropriately evaluated via this assay. Consequently, multicolor FISH-based methods could be widespread applied in human genetics, reproductive medicine, especially genetic toxicology. In this paper, the progress in regard was reviewed.

Animals↗
PubMed1987

Simulation of genetic control of reproduction in beef cows. II. Derived genetic parameters.

A stochastic computer simulation model was used to predict heritability (h2) and repeatability (t) of derived reproductive traits in beef cattle as a function of underlying, normally-distributed genetic variation in interval from calving to first estrus (postpartum interval) and single-service conception rate. Traits simulated were mating rate, first-service conception rate, overall conception rate, date of first service, number of services during a 63-d breeding season, calving date and postpartum interval. Weight of calf weaned was also simulated on a per-cow-exposed, per-cow-mating, per-cow-calving, per-calf-weaned or adjusted 205-d basis. Derived estimates of h2 for mating rate and date of first service were not significantly different from 0, reflecting the high proportion of cows that were predicted to cycle within the first 21 d of breeding. Estimates of h2 were significant and approached the level of input h2 for overall and first-service conception rate and number of services, suggesting that these traits may be potential selection criteria. Values of h2 for calving date were significant but considerably smaller than input h2. Estimates of t were much larger than h2 for date of first service and calving date, even when no nonadditive genetic or permanent environmental effects were explicitly simulated. Estimates of h2 for weaning weight per cow exposed and especially for weaning weight per cow calving (in the presence of random calf death losses) were much lower than underlying h2 values. Culling of open cows generally reduced genetic variances of derived reproductive traits to negligible levels within three calf crops.

Animals↗
PubMed1993

Essentialism, which essentialism? Some implications of reproductive and genetic techno-science.

New technologies, such as genetic screening, artificial insemination, in vitro fertilization, and pre-natal diagnosis, have given new meaning to human reproduction. Such innovations make clear that marriage, procreation, and the biological family are not the sole "natural" means of perpetuating the human race. One would have hoped that these inventions would eventually have raised in public regard the gay/lesbian family to the same level as heterosexuality and the biological family. Franklin shows, however, that the old heterosexual essentialism is preserved by government restricting the use of the new technologies to two-parent families consisting of both mother and father. What should have resulted in the erosion of heterosexual privilege has, instead, led to its reinforcement. Franklin draws a parallel with the AIDS epidemic which could have been the opportunity to spread knowledge and acceptance of varied forms of sexuality but has instead been used to shore up a traditional sexual morality and a renewed vilification of homosexuality.

Female↗
PubMed1993

Fertility, reproduction, and genetic disease: studies on the mutagenic effects of environmental agents on mammalian germ cells.

Because genetically based diseases have a major impact on human health, the National Institute of Environmental Health Sciences (NIEHS) has conducted a research and testing program for more than a decade to address chemical induction of heritable genetic damage in the germ cells of mammals. Although most genetic disease results from preexisting mutations, a portion is due to the occurrence of new mutations. The supposition that exposure to mutagenic chemicals contributes to the occurrence of new mutations in the human population is strongly supported by the results from animal models. Such studies clearly demonstrate the potential of environmental chemicals to induce mutations in both somatic and reproductive cells of mammals. This NIEHS program has become a leader in the identification of genetic hazards in the environment and in the acquisition of animal model data used by regulatory agencies in assessing genetic risks to human health.

Animals↗
PubMed1999

Genetic structure, reproductive biology and ecology of isolated populations of asplenium csikii (Aspleniaceae, pteridophyta)

The potential for environmental heterogeneity to generate spatial structuring of genotypes in seed-plant populations that occupy patchy habitats has been demonstrated by several studies, but little is known about the population structure of pteridophytes occupying patchy environments. In this study we have examined the genetic structure of isolated populations of the rock fern Asplenium csikii, an ecological specialist, growing almost exclusively on perpendicular walls of natural rock outcrops. All genetic variation observed in this taxon was partitioned between localities; no allozyme variation was found within a site and each site was colonized by a single multilocus phenotype (MLP). In total, five different MLPs were recorded from the nine localities, with two MLPs present at more than one site. Previous examination of population structure and genetic diversity in another rock fern, A. ruta-muraria, showed that the genetic diversity increases through multiple colonization over time. However, we cannot find any such correlation for A. csikii. All populations are genetically uniform, despite the probably considerable age of the populations and sites. Earlier studies concluded that the ample production of wind-borne propagules would lead to multiple colonization of sites and that reproductive features, such as single-spore colonization and subsequent intragametophytic selfing, would lead to very little genetic structuring of fern populations. In contrast to this prediction, it appears that ecological specialization and the scarcity of the narrowly defined niche contribute strongly to the pronounced partitioning of genetic variability observed in populations of A. csikii.

Journal Article↗
PubMed1984

Reproductive and genetic effects of continuous prenatal irradiation in the pig.

The stem germ cells of the prenatal pig are highly vulnerable to the cytotoxic effects of ionizing irradiation. This study was conducted to determine whether sensitivity to killing was also marked by a sensitivity to mutation and how prenatal depletion of the germ-cell population affects reproductive performance. Germ-cell populations were reduced by continuously irradiating sows at dose rates of either 0.25 or 1.0 rad/day for the first 108 days of gestation. The prenatally irradiated boars were tested for sperm-producing ability, sperm abnormalities, dominant lethality, reciprocal translocations, and fertility. Prenatally irradiated females were allowed to bear and nurture one litter, then tested for dominant lethality in a second litter; germ cell survival and follicular development were assessed in their serially sectioned ovaries. Sperm production was not significantly affected in the 0.25-rad boars, but boars irradiated with 1.0 rad per day produced sperm at only 17% of the control level. Incidence of defective sperm was 4.9% and 11.1% in the 0.25 and 1.0 groups, respectively. Four of the 1.0-rad boars were infertile, but prenatal irradiation apparently caused neither dominant lethality nor reciprocal translocations in fertile males. Number of oocytes was reduced to 66 +/- 7% of control in the 0.25-rad gilts, but reproductive performance was unaffected and no dominant lethality was observed. Only 7 +/- 1% of the oocytes survived in the 1.0-rad group. Reproductive performance was normal for the first litter, but four of the 23 sows tested were infertile at the second litter and a significant incidence of dominant lethality was observed.(ABSTRACT TRUNCATED AT 250 WORDS)

Abnormalities, Radiation-Induced↗