scholarly journals Plumage colours Stability in Inbreed Pelung Chicken

2021 ◽  
Vol 33 ◽  
pp. 01005
Author(s):  
Hendry T.S.G. Saragih ◽  
Ayudha B.I. Perdamaian ◽  
Sadiman ◽  
Iwan Roosdianto ◽  
Budi S. Daryono

Pelung is one of the most importance local chicken in Indonesia. Genetic introgression and inbreeding depression were the major threat for local chicken gene pool. The objective of this research was to investigate the effect of serial inbreeding mating to plumage colours of Pelung chicken. Pure Pelung chicken which purchased from Cianjur sub-district was undergo full-sib mating through five generation. All offspring phenotypes was recorded. The results show gradual plumage phenotype change of inbreed Pelung chicken. Initially, adult male chicken had Black-red coloured as wildtype (WT) shifted to partridge and black-silver coloured in later generations. The current findings indicating that inbreeding made recessive traits to be expressed which some of them might had deleterious effect. Random mating should be maintained to preserve genetics stability of Pelung chicken

2019 ◽  
Author(s):  
Zeynab Bagheri ◽  
Ali Asghar Talebi ◽  
Sassan Asgari ◽  
Mohammad Mehrabadi

AbstractWolbachia are intracellular α-proteobacteria that have a wide distribution among various arthropods and nematodes. They affect the host reproduction favoring their maternal transmission, which sets up a potential conflict in inbreeding situations when the host avoids sexual reproduction preventing inbreeding depression, while Wolbachia pushes it. In this study, we used the wasp Habrobracon hebetor to test the hypothesis that Wolbachia modulate inbreeding avoidance behaviour and promote sib mating. To test this, we first cured wasps of Wolbachia using tetracycline treatment and produced infected and uninfected isolines. Then, we paired the uninfected and infected females with sibling (inbred) and non-sibling (outbred) males in choice and non-choice experiments. Our results showed no obvious precopulatory inbreeding avoidance in this wasp as brother-sister mating rates (in both choice and nonchoice experiments) were not significantly different form non-sibling pairs, regardless of Wolbachia infection. However, our results indicated that H. hebetor shows a strong postcopulatory inbreeding avoidance behaviour that results in a low fertilization rate of uninfected siblings and therefore high rate of production of male progeny was obtained. We observed higher rates of fertilization success in the Wolbachia-infected lines that resulted in significantly higher female progeny production compared to the uninfected sib mates. Since diploid females are the result of successful fertilization due to haplodiploidy sex determination system in this insect, our results indicate that Wolbachia promoted fertile sib mating in H. hebetor. Interestingly, the rate of adult emergence in the progeny of Wolbachia-infected sib mates were almost similar to the non-sib mate crosses and significantly more than those observed in the uninfected sib mate crosses. We support the idea that Wolbachia modulate inbreeding avoidance and promote sib mating and also mitigate inbreeding depression. The wasp Habrobracon hebetor siblings infected with Wolbachia show higher rates of fertilization success and higher adult emergence rates compared to the uninfected sib mates. By promoting successful sex with siblings and increasing the probability of female progeny, Wolbachia enhance their transmission to the next generation and also mitigate inbreeding depression. This is an undescribed effect of Wolbachia (symbiont) on the host reproduction.


Author(s):  
Donald M. Waller ◽  
Lukas F. Keller

Inbreeding (also referred to as “consanguinity”) occurs when mates are related to each other due to incest, assortative mating, small population size, or population sub-structuring. Inbreeding results in an excess of homozygotes and hence a deficiency of heterozygotes. This, in turn, exposes recessive genetic variation otherwise hidden by heterozygosity with dominant alleles relative to random mating. Interest in inbreeding arose from its use in animal and plant breeding programs to expose such variation and to fix variants in genetically homogenous lines. Starting with Gregor Mendel’s experiments with peas, geneticists have widely exploited inbreeding as a research tool, leading R. C. Lewontin to conclude that “Every discovery in classical and population genetics has depended on some sort of inbreeding experiment” (see Lewontin’s 1965 article “The Theory of Inbreeding.” Science 150:1800–1801). Charles Darwin wrote an entire book on the effects of inbreeding as measured in fifty-two taxa of plants. He and others noted that most plants and animals go to great length to avoid inbreeding, suggesting that inbreeding has high costs that often outweigh the benefits of inbreeding. Benefits of inbreeding include increased genetic transmission while the costs of inbreeding manifest as inbreeding depression when deleterious, mostly recessive alleles otherwise hidden as heterozygotes emerge in homozygote form upon inbreeding. Inbreeding also reduces fitness when heterozygotes are more fit than both homozygotes, but such overdominance is rare. Recurrent mutation continuously generates deleterious recessive alleles that create a genetic “load” of deleterious mutations mostly hidden within heterozygotes in outcrossing populations. Upon inbreeding, the load is expressed when deleterious alleles segregate as homozygotes, causing often substantial inbreeding depression. Although inbreeding alone does not change allele frequencies, it does redistribute genetic variation, reducing it within families or populations while increasing it among families or populations. Inbreeding also increases selection by exposing deleterious recessive mutations, a process called purging that can deplete genetic variation. For all these reasons, inbreeding is a central concept in evolutionary biology. Inbreeding is also central to conservation biology as small and isolated populations become prone to inbreeding and thus suffer inbreeding depression. Inbreeding can reduce population viability and increase extinction risk by reducing individual survival and/or reproduction. Such effects can often be reversed, however, by introducing new genetic material that re-establishes heterozygosity (“genetic rescue”). The current availability of DNA sequence and expression data is now allowing more detailed analyses of the causes and evolutionary consequences of inbreeding.


1967 ◽  
Vol 10 (1) ◽  
pp. 73-80 ◽  
Author(s):  
J. C. McCarthy

Twenty-four lines were bred from a base population of outbred Q mice by continued full-sib mating. Inbreeding depression in litter size at birth was observed. This decline in litter size was analysed in terms of ovulation rate, the incidence of preimplantation mortality and the incidence of postimplantation mortality. Pregnant females were dissected at 17½ days' gestation and the numbers of corpora lutea, or eggs, and of live and dead embryos were counted. Matings were arranged so that separate estimates of the effects of inbreeding in the mother and in the litter on the components of litter size could be obtained.In the first generation of inbreeding when the inbreeding coefficient of the litter was raised from 0 to 25% decline in litter size was attributable to an increased incidence of preimplantation mortality.In the second and fourth generations decline in litter size was attributable to (1) a reduction in the number of eggs ovulated by the inbred mothers, (2) an increased incidence of preimplantation mortality which resulted from inbreeding in the mother. No evidence of significant effects on mortality of inbreeding in the litter was obtained in the later generation of inbreeding.These findings are discussed in the context of previous work on the effects of inbreeding and crossing on litter size and its components in mice and pigs.


1978 ◽  
Vol 40 (3) ◽  
pp. 591-594 ◽  
Author(s):  
Urmila Pingle ◽  
B. V. Ramasastri

1. Amaranthus spp. leaves contain high amounts of oxalates which affect the calcium absorption. This study was done to determine whether removal of the water-soluble oxalates from the leaves by cooking would reduce this deleterious effect.2. Experimental work done with two types of basal diets on six adult male subjects has shown that the milk Ca absorption was low when leaves cooked without draining away the water were included in the diet. However when the soluble oxalates were removed by throwing away the water after cooking the leaves, the absorption of milk Ca was unaffected.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Joanna Obrzut ◽  
Jolanta Calik ◽  
Józefa Krawczyk

Abstract The aim of the study was to determine trends in performance and hatchability traits of eight strains of hens that have been covered by the gene pool protection programme in Poland over ten years/generations. The study involved conservation populations of laying hens: Greenleg Partridge (Z-11), Yellowleg Partridge (Ż-33), Sussex (S-66), Leghorn (H-22, G99), Rhode Island Red (R-11, K-22) and Rhode Island White (A-33), which were maintained at the Experimental Station of the National Research Institute of Animal Production in Chorzelów. The following productive traits were analysed for each population: body weight at 20 wk (g), egg weight at 33 and 53 wk, sexual maturity and number of eggs laid per hen up to 56 wk of age. Mortality and culling were also recorded during rearing and production periods. Furthermore, effective population size (Ne) and inbreeding coefficient in the population (Fx) were calculated for each strain. The analysis of the performance results of the eight strains of hens and their trends indicate that the methods of conservation breeding adopted for these populations enable effective implementation of the conservation programme. The strains were found to differ in all the performance traits subjected to evaluation. Over the 10 generations, the strains examined showed high survival and hatchability parameters during both rearing and production periods. The currently used random mating system proved effective to prevent the populations from an increase of inbreeding. However, a worrying downward trend in body weight was observed in some strains.


2018 ◽  
Vol 22 (2) ◽  
pp. 68
Author(s):  
Hasnelly . ◽  
Sofjan Iskandar ◽  
Tike Sartika

<p>One of local chicken breeds develop in Indonesian Research Institute for Animal Production (IRIAP) is local SenSi-1 Agrinak chicken. This new improved local-meat-type breed was released with Ministry Agriculture Decree Number 39/Kpts/PK.020/1/2017 on 20<sup>th</sup> January 2017. SenSi-1 Agrinak was originally selected from native Sentul chicken breed obtained from Ciamis district in West Java Province. Selection criteria were two feather colors of grey or black spotted white (pucak), which were applied to both males and females. Pea-comb type was also one criterion for males, applied at the age of 10 weeks. Live weight at the age of 10 weeks with the selection intensity of 25% was applied to each generation of males chicken. Selection proceeded for six generations. Selection program was carried out under standard feed formulae containing around 17% crude protein with 2850 kcal ME/ kg, and containing other nutrients following the ones recommended for modern chicken of White Leghorn. Observation was conducted on each of about 2000 young chickens of grey and of Pucak SenSi-1 Agrinak both males and females age of 10 and 84 weeks. Results showed that grey SenSi-1 Agrinak chicken in total population, had: i) Grey feather color distribution of 55.51% in males, and 60.77% in females; ii) Yellow shank color of 52.51% in males, and 33.33% in females; iii) Pea type comb of 90.98% in males, and 89.23% in females; iv). Ten weeks live weight of 886.38+142.93 g/bird in males, and 739.17+ 118.87 in females. Pucak SenSi-1 Agrinak chicken in total population, had: i) Pucak feather color of 75.65% in males, and 8330% in females; ii) Yellow shank color of 51.91% in males, and 36.59% in females; iii) Pea type comb of 91.55% in males, and 92.28% in females; iv) Ten weeks live weight of 908.76+ 130.98 g/bird in males, and 750.53+ 110.56 g/bird in females. Whilst for grey SenSi-1 Agrinak male chicken after selection had live weight at 10 weeks old of 1015+107 g/bird, and for Pucak SenSi-1 Agrinak male chicken was 1051+76 g/bird. This initial performance information for those two breeds of considerably improved local chicken can be used as the base of information for SenSi-1 Agrinak breed for male line of meat type of local chicken breeding.</p>


2010 ◽  
Vol 92 (2) ◽  
pp. 127-140 ◽  
Author(s):  
SHU-RONG ZHOU ◽  
JOHN R. PANNELL

SummaryInbreeding depression has important implications for a wide range of biological phenomena, such as inbreeding avoidance, the evolution and maintenance of sexual systems and extinction rates of small populations. Previous investigations have asked how inbreeding depression evolves in single and subdivided populations through the fixation of deleterious mutations as a result of drift, as well as through the expression of deleterious mutations segregating in a population. These studies have focused on the effects of mutation and selection at single loci, or at unlinked loci. Here, we used simulations to investigate the evolution of genetic load and inbreeding depression due to multiple partially linked loci in metapopulations. Our results indicate that the effect of linkage depends largely on the kinds of deleterious alleles involved. For weakly deleterious and partially recessive mutations, the speed of mutation accumulation at segregating loci in a random-mating subdivided population of a given structure tends to be retarded by increased recombination between adjacent loci – although the highest numbers of fixation of slightly recessive mutant alleles were for low but finite recombination rates. Although linkage had a relatively minor effect on the evolution of metapopulations unless very low values of recombination were assumed, close linkage between adjacent loci tended to enhance population structure and population turnover. Finally, within-deme inbreeding depression, between-deme inbreeding depression and heterosis generally increased with decreased recombination rates. Moreover, increased selfing reduced the effective amount of recombination, and hence the effects of tight linkage on metapopulation genetic structure were decreased with increasing selfing. In contrast, linkage had little effect on the fate of lethal and highly recessive alleles. We compare our simulation results with predictions made by models that ignore the complexities of recombination.


2019 ◽  
Vol 2019 (1) ◽  
pp. 66-81 ◽  
Author(s):  
James J Bull ◽  
Christopher H Remien ◽  
Stephen M Krone

AbstractBackground and objectivesGenetic engineering combined with CRISPR technology has developed to the point that gene drives can, in theory, be engineered to cause extinction in countless species. Success of extinction programs now rests on the possibility of resistance evolution, which is largely unknown. Depending on the gene-drive technology, resistance may take many forms, from mutations in the nuclease target sequence (e.g. for CRISPR) to specific types of non-random population structures that limit the drive (that may block potentially any gene-drive technology).MethodologyWe develop mathematical models of various deviations from random mating to consider escapes from extinction-causing gene drives. A main emphasis here is sib mating in the face of recessive-lethal and Y-chromosome drives.ResultsSib mating easily evolves in response to both kinds of gene drives and maintains mean fitness above 0, with equilibrium fitness depending on the level of inbreeding depression. Environmental determination of sib mating (as might stem from population density crashes) can also maintain mean fitness above 0. A version of Maynard Smith’s haystack model shows that pre-existing population structure can enable drive-free subpopulations to be maintained against gene drives.Conclusions and implicationsTranslation of mean fitness into population size depends on ecological details, so understanding mean fitness evolution and dynamics is merely the first step in predicting extinction. Nonetheless, these results point to possible escapes from gene-drive-mediated extinctions that lie beyond the control of genome engineering.Lay summaryRecent gene drive technologies promise to suppress and even eradicate pests and disease vectors. Simple models of gene-drive evolution in structured populations show that extinction-causing gene drives can be thwarted both through the evolution of sib mating as well as from purely demographic processes that cluster drive-free individuals.


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