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Failure of inbreeding to influence pineal-induced gonadal regression in short day exposed hamsters.

The rate of testicular degeneration and the drop in plasma testosterone levels were compared in what were referred to as short-term domesticated (STD) and long-term domesticated (LTD) Syrian hamsters when they were maintained under short photoperiodic conditions (light:dark cycles of 10:14). STD hamsters were derived from wild stock captured in 1971; LTD animals were derived from the original stock captured in 1930. The rate of testicular degeneration as well as the fall in plasma testosterone levels were similar in both groups of animals. After 26 weeks exposure to short days, the testes and accessory sex organs regenerated to the fully mature state in both the STD and LTD animals; likewise, plasma testosterone levels had returned to normal in both groups. Pineal melatonin levels of STD and LTD female hamsters were compared during both the light phase (2000 and 0800hr) and dark phase (0200 and 0400hr) of the daily light:dark cycle. These animals were kept under photoperiodic conditions of 14:10 with lights on daily from 0600-2000hr. Day- and night-time levels of pineal melatonin were similar in both groups of hamsters. The results indicate that inbreeding does not influence the atrophic response of the reproductive organs of male hamsters to short day exposure or the ability of the pineal gland to produce melatonin.

Animals↗

Inbreeding effects on traits with and without selection for part record rate of lay in chickens.

Data from inbred lines, one (D) selected for part record rate of lay and the other (C) unselected for any trait, were analyzed. After 19 generations of continuous full sib matings, the C line showed significant decreases in part record egg number, 32-week egg weight, shell thickness, full record egg number and part record rate of lay but nonsignificant decreases in hatchability, full record rate of lay, and laying house mortality. Age at first egg, Haugh unit and mature body weight showed significant increases in this line. The D line was similar to the C line in its response to the same intensity of inbreeding for all traits except full record egg number, part record rate, and fertility, each of which showed a significant decrease, and Haugh unit and full record rate of lay, which showed nonsignificant increases. Results indicated that the small advantages selection conferred on the inbred line in part record rate of lay (the selection criterion), full record egg number, and full record rate of lay were accompanied by undesirable changes in other traits, resulting in later sexual maturity, larger body weight, lower Haugh unit, fertility, and hatchability compared with the unselected line.

Animals↗

[Truncation family selection and nonsystematic inbreeding leads to a rapid fixation of a pattern of mobile genetic elements in a computer model].

A computer simulation model of the population dynamics of a polygenic system and a pattern of mobile genetic elements (MGEs) under directional truncation selection for a quantitative trait was developed. Modifier MGEs were shown to be rapidly and adaptively fixed (or lost) together with the modified polygenes. Marker MGEs and independent MGE copies were fixed and lost just as rapidly but in a random manner. Using specific marking of initial haploid genomes and direct computing of the mean proportion of identical encounters at each locus in each generation, it was shown that the mean nonselective inbreeding coefficient F(n) dramatically increases in the course of selection, reaching values 0.7-0.9 in 15-20 generations. As a result, adaptive homozygotization of polygenes and modifier MGEs and random homozygotization of marker MGEs, independent MGE copies, and all other genes of the genome occurs. These results confirm the hypothesis on the "champion" polygene pattern advanced earlier to explain the data of selection experiments.

Animals↗

[Inbreeding in the population and the spread of schizophrenia in one of the rural regions of Azerbaijan].

The investigation was carried out in Pushkin region of Azerbaijan SSR. The coefficient of inbreeding was found to be 0,01306 and 0,01142 in 2 typical villages; the frequency of consanguineous marriage in both villages was 30%. The occurence of consanguineous marriage is explained by a little migration of the population, large families and a stability of marriage traditions. An increased frequency of parental consanguinities of sporadic schizophrenic patients in comparison with the average one was found. This indicates the determination of some cases by rare recessive genes.

Azerbaijan↗

[Inbreeding, endogamy and exogamy among relatives of schizophrenia patients].

An increased frequency of consanguineous marriages among the parents of schizophrenic patients in comparison with the control group of exogenous-somatic patients (infections, trauma) was found. Endogamy among the parents of schizophrenic patients and the control group was practically the same. The data obtained indicate a certain, but not the leading, role of inbreeding in the etiology of schizophrenia.

Azerbaijan↗

[Characteristics of inbreeding of the population and distribution of schizophrenia in one of the rural regions of Azerbaijan].

The investigation was carried out in Pushkin region of Azerbaijan SSR. The coefficient of inbreeding was found to be 0,01306 and 0,01142 in 2 typical villages; the frequency of consanguineous marriage in both villages was 30%. The occurrence of consanguineous marriage is explained by a little migration of the population, large families and a stability of marriage traditions. An increased frequency of parental consanguinities of sporadic schizophrenic patients in comparison with the average one was found. This indicates the determination of somes cases by rare recessive genes.

Azerbaijan↗

Equilibrium under inbreeding in balanced polymorphisms.

The results of a study on frequencies of genes causing lethal or sublethal disease are reported in relation to the level of consanguinity and heterozygote advantage in populations. The theoretical background of the population dynamics of genes under heterozygote advantage and in the presence of inbreeding is examined and the theoretical models are applied to the estimation of the level of heterosis for lethal and sublethal genes that are responsible for important public health problems in certain populations; these problems include beta-thalassaemia and sickle-cell anaemia. Estimates obtained from the proposed models show a high degree of internal consistency under widely different conditions; data on sickle-cell anaemia from several African populations and on beta-thalassaemia from Italy and Malta were analysed. The hypothesis that rare lethal genes, such as those for Tay-Sachs disease, are maintained in the human population by heterozygote advantage is examined and discussed.

Anemia, Sickle Cell↗

New mutant rabbit strain with hypercholesterolemia and atherosclerotic lesions produced by serial inbreeding.

We have investigated the characteristics of the Kurosawa and Kusanagi hypercholesterolemic (KHC) rabbit, a strain manifesting inherited and persistent hypercholesterolemia and produced by inbreeding from mutants discovered in 1985. These KHC rabbits had abnormally high serum cholesterol, triglyceride, and phospholipid concentrations 8 to 10 times greater than the concentrations in clinically normal Japanese white rabbits (Oryctolagus cuniculus). The KHC rabbits also had decreased serum high-density lipoprotein cholesterol concentration, about one-third the value in clinically normal rabbits. In addition, the serum lipoprotein electrophoretic patterns were characterized by a strong, broad beta-lipoprotein band and a diminished alpha-lipoprotein band. Fractionation of lipoprotein lipids revealed increased cholesterol, phospholipid, and triglyceride in the low-density lipoprotein fraction; increased cholesterol and phospholipid in the very low-density lipoprotein fraction; and decreased cholesterol and triglyceride in the high-density lipoprotein fraction. On the basis of incidence of hypercholesterolemia in mating experiments, this abnormality is thought to have been inherited as a single autosomal recessive gene mutation, and analysis of the low-density lipoprotein receptor indicated that the KHC rabbit has a 12-base pair deletion in the low-density lipoprotein receptor mRNA. Macroscopic analysis of the aorta revealed the atheromatous lesions at 2 months of age, drastically increased lesional areas in the total aortic surface at 8 months of age, and a high incidence of coronary atheromas and xanthomas. Light microscopy revealed two typical lesions in the aorta fatty plaque and medical calcification.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[Population genetics processes in animal generations with brother X sister inbreeding and the absence of selection].

Fifteen distinct isolates of the progeny with a homozygosity ranging from 0 to 87.5% are formed in the model population of Drosophila melanogaster as a result of a systematic inbreeding "brother X sister". In these isolates 336 different variants are formed. The genetic regularity of segregation of each isolate variant for homozygosity in the subsequent generation of the progeny at such a mating type and the variability of mean homozygosity were determined.

Animals↗

[Inbreeding and the pedigree value of sires].

The influence of bull fathers' pedigree values and the influence of the type of the selection have been studied from the viewpoint of heritability of the selective traits in "father-son-grandfather" generations. The trend of positive influence of inbreeding on bulls' pedigree values has been studied from the viewpoint of milk yield in their daughters.

Animals↗

[A theoretical analysis of systematic "parents X progeny" inbreeding in animals in the absence of selection].

Theoretical analysis of the structure of a model population of D. melanogaster under systematic inbreeding--"parents x progeny"--has been conducted using a computer and the original method elaborated. Theoretical relationships between the development of homozygous isolated groups of progeny of 30 generations and their backcrosses with heterozygous and homozygous common ancestors A male and B female were established.

Animals↗

Expectations for inbreeding depression on self-fertilization of tetraploids.

The contribution to the inbreeding depression from a digenic tetrasomic locus upon self-fertilization involves three genotypic interaction effects which may be thought of as a generalization of the dominance deviation for a diploid locus. It is shown how this contribution may be expressed in terms of these genotypic interaction effects, the gene frequencies and the number of generations of selfing.

Alleles↗

Lay perceptions of genetic risks attributable to inbreeding in Pakistan.

Pakistan along with many other West and South Asian countries has a very high prevalence of consanguineous, especially close cousin, marriages. Although there is substantial empirical information on offspring morbidity and mortality attributable to parental consanguinity, population-based information on how communities in general, and women in particular, perceive the health risks associated with consanguineous unions is limited. This paper considers community perceptions of health effects associated with consanguineous marriages using qualitative data from 15 focus group discussions and 294 in-depth interviews. The study was conducted in four low-income, multi-ethnic, and multi-religious communities in Karachi, the principal commercial center of Pakistan. The results show a general lack of awareness of the possible adverse health effects of consanguineous marriage. In cases where a link between consanguinity and ill health was acknowledged, it often centered on the familial origins of non-communicable disorders such as diabetes and hypertension or infectious diseases such as tuberculosis. Belief in fate and the "evil eye" was widespread across all ethnic and religious groups. Many respondents did not agree with medical explanations of a genetic mode of disease inheritance, even in cases where there was an affected child in the family. The absence of a uniform manifestation of disease among all children of a couple who were identified as carriers of a specific mutation added to the confusion among participants. The study highlights the need for further quantification of risks associated with consanguinity and a need for provision of appropriate information to primary-care clinicians and also to communities. The likely impact of increasing morbidity attributable to inbreeding on the health care system in resource poor settings is also discussed.

Adolescent↗

Family composition and menarcheal age: anti-inbreeding strategies.

Family composition (e.g., the absence of a father) is associated with pubertal timing in women, although the socioendocrinology of the human primate is poorly understood. To better understand social influences on sexual maturation, retrospective data were collected on menarcheal age and family composition from a sample of approximately 1,938 participants from a college population. Absence of a biological father, the presence of half- and step-brothers, and living in an urban environment were associated with earlier menarche. The presence of sisters in the household while growing up, especially older sisters, was associated with delayed menarche. Menarcheal age was not affected by number of brothers in the household, nor was there an effect of birth order. Body weight and race were also associated with menarche. The present findings advance the literature as they are suggestive of putative human pheromones that modulate sexual maturation to promote gene survival and prevent inbreeding, as occurs in rodents and nonhuman primates.

Adolescent↗

Inbreeding from isonymy and repeated pairs of surnames in the Ebro Delta region (Tarragona, Spain).

The aim of the study was to evaluate the levels of inbreeding calculated from isonymy with its random (Fr) and nonrandom (Fn) components, and repeated pairs of surnames (RP2) and their random component (RP2r) in the Ebro River Delta region (Tarragona, Spain). This region is made up of four parishes, and data correspond to the period 1939-1995. The global results are on the same levels as observed in other studies, but the values obtained in 3 of 4 parishes are relatively high. The Fn global value is higher than Fr, as opposed to what happens in each parish, so there is a clear Wahlund effect of subdivision of the region into parishes. Among the parishes there is a clear differentiation for Amposta, with values much lower than for the rest, due to the behavior of this population, i.e., a high immigration rate.

Consanguinity↗

Inbreeding effect on morbidity: I. Three analyses (one with cousin and sib controls) of two surveys among Brazilian whites and Negroes.

Data from two surveys performed in Brazil and involving 5,719 persons have been subdivided into three subsamples (one with cousin and sib controls). The totals led to estimates of B (abnormal equivalents per gamete) around 0.5, of A (the damage in a noninbred population) around 0.01-0.02, and of B/A from 14 to 77. No statistically significant difference was found between whites and nonwhites (mulattoes and Negroes). Inbreeding seems to disclose a predominantly mutational load.

Brazil↗

Inbreeding effect on morbidity: II. Analyses of a third survey including and excluding infant-juvenile mortality among Brazilian whites and Negroes.

Data on a survey involving 10,458 liveborn white and nonwhite (mulattoes and Negroes) persons have been analyzed to estimate B, A, and B/A for anomalies in general, both including and excluding infant-juvenile mortality. In both instances and race groups, the approximate estimates of those parameters were 0.5, 4.5, and 12. Inbreeding seems to disclose a predominantly mutational load.

Adolescent↗