Academic literature on the topic 'Dobzhansky-Muller Model'

Background: Approximately 80% of all viruses are RNA viruses and they contain their specific RNA helicases. Defective RNA helicases have been linked to infectious diseases (Viral Infections). Materials and Methods: The articles have gone through many types of research from the beginning of the epidemic of Coronaviruses through history and we introduced the neglected hypothesis of Shifting balance theory, Bateson–Dobzhansky–Muller model & Quantum evolution. In the ancestral population, the genotype is AABB. When two populations become isolated from each other, new mutations can arise. In one population A evolves into a, and in the other B evolves into b. When the two populations hybridize it is the first time A and B interact with each other. When these alleles are incompatible, we speak of Dobzhansky–Muller incompatibilities plus the role of MMA in mitochondria in spreading SARS-CoV-19 through populations and the result of an infection in COVID-19. Results: In viruses specifically COVID-19, Ribosomal Frameshift is programmed to allows the virus to encode multiple types of proteins from the same mRNA. HIV-1 (human immunodeficiency virus), RSV (Rous sarcoma virus), and all types of influenza viruses use Ribosomal Frameshift. they rely on frameshifting to create a proper ratio of normal translation and trans-frame (encoded by frameshifted sequence) proteins. Notably, its use in viruses is primarily for compacting more genetic information into a shorter amount of genetic material. Conclusion: to find the genome sequence of COVID-19 we also used Nanopore sequencing that introduced and manufactured by Oxford scientists, due to differences in the action of infection in the host, we could not reach any results since the Novel Virus has not a stable genome (which is quite dynamic) since through our deep research, each virus contains its specific genome sequencing and we cannot claim that COVID-19 has one specific genome sequence like MERS-CoV, SARS-CoV or any types of viruses which has been discovered and contains their specific genome.

Abstract Speciation is a process whereby the evolution of reproductive barriers leads to isolated species. Although many studies have addressed large-effect genetic footprints in the advanced stages of speciation, the genetics of reproductive isolation in nascent stage of speciation remains unclear. Here, we show that pig domestication offers an interesting model for studying the early stages of speciation in great details. Pig breeds have not evolved the large X-effect of hybrid incompatibility commonly observed between “good species.” Instead, deleterious epistatic interactions among multiple autosomal loci are common. These weak Dobzhansky–Muller incompatibilities confer partial hybrid inviability with sex biases in crosses between European and East Asian domestic pigs. The genomic incompatibility is enriched in pathways for angiogenesis, androgen receptor signaling and immunity, with an observation of many highly differentiated cis-regulatory variants. Our study suggests that partial hybrid inviability caused by pervasive but weak interactions among autosomal loci may be a hallmark of nascent speciation in mammals.

Hybridization is a potent mechanism for generating unique strains with broad host ranges and increased virulence in fungal pathogens. In the opportunistic basidiomycete pathogen Cryptococcus neoformans, intervarietal hybrids are commonly found infecting patients. The two parental varieties C. neoformans var. grubii and C. neoformans var. neoformans mate readily under laboratory conditions, but the hybrid basidiospores have germination rates about four times lower than those from intravarietal crosses. Here, we used microdissection to collect basidiospores from a hybrid cross and analysed the genotypes of germinated basidiospores to identify potentially antagonistic allelic combinations between loci that impact basidiospore germination. Our analyses showed clear evidence for Bateson–Dobzhansky–Muller (BDM) incompatibility affecting basidiospore viability. Antagonistic combinations of alleles from both two loci and three loci were found. Interestingly, most of the hybrid progeny showed segregation distortion in favour of the alleles from var. neoformans, consistent with large-scale epistatic interactions among loci affecting basidiospore viability. Our study presents the first evidence of BDM incompatibility between nuclear genes affecting post-zygotic reproductive isolation in this model basidiomycete yeast.

The term “genetic load” first emerged in a paper written in 1950 by the geneticist H. Muller. It is a mathematical model based on biological, social, political and ethical arguments describing the dramatic accumulation of disadvantageous mutations in human populations that will occur in modern societies if eugenic measures are not taken. The model describes how the combined actions of medical and social progress will supposedly impede natural selection and make genes of inferior quality likely to spread across populations – a process which in fine loads their progress. Genetic load is based on optimal fitness and emerges from a “typological view” of evolution. This model of evolution had previously, however, been invalidated by Robert Wright and Theodosius Dobzhansky who, as early as 1946, showed that polymorphism was the rule in natural populations. The blooming and persistence of the concept of genetic load, after its theoretical basis had already expired, are a historical puzzle. This persistence reveals the intricacy of science and policy-making in eugenic matters. The Canguilhemian concept of ‘scientific ideology’ (1988) is used along with the concept of ‘immutable mobile’ (Latour 1986) and compared with the concept of ‘co-production’ (Jasanoff 1998), to provide complementary perspectives on this complex phenomenon.

Wolbachien sind intrazeklluläre Bakterien die zahlreiche Arthropodenarten infizieren. Sie induzieren häufig eine zytoplasmatische Paarungsinkompatibilität die postzygotische Isolation zwischen unterschiedlich infizierten Individuen der gleichen Wirtsart verursacht, weswegen Wolbachien Beachtung als mögliche Katalysatoren von Artbildungsprozessen gefunden haben. Vorherige Arbeiten zur Artbildung untersuchten meist entweder Wolbachia-induzierte oder die klassischen, genetischen postzygotischen Isolationsmechanismen. Normalerweise sollte es aber der Fall sein dass beide Mechanism gleichzeitig auftreten. In dieser Arbeit führen wir Untersuchungen zur Rolle der Wolbachien in der Artbildung fort indem wir die Interaktionen von Wolbachia-induzierten und genetischen Inkompatibilitäten analysieren. Wir werden zeigen dass Wolbachien einen starken Einfluss auf genetisch-basierte Artbildungsprozesse haben. Insbesondere können sich die Mechanism bei gleichzeitigem Auftreten katalysieren. Außerdem werden wir zeigen dass Wolbachia Artbildungsprozesse unter allgemeineren Bedingungen beeinflussen kann als vorherige Studien suggerierten. Da die Rolle der Wolbachien in der Artbildung stark von deren Verbreitung abhängt, werden wir desweiteren eine statistische Metaanalyse von bestehenden Daten zu Infektionsfrequenzen präsentieren. Aufgrund der Methoden der Datenerhebung ist es sehr wahrscheinlich, dass der wirkliche Anteil der infizierten Arten mit 20% deutlich unterschätzt wird. Unsere Analyse bestätigt dies und zeigt dass viel wahrscheinlicher circa zwei Drittel aller Arten infiziert sind. Unsere Resultate der klassischen Artbildungstheorie kombiniert mit denen der statistischen Analyse zu Infektionsfrequenzen von Wolbachia implizieren dass Wolbachien als allgemeine Faktoren in der Evolution von Arthropoden anzusehen sind.<br>Wolbachia are intracellular bacteria that commonly infect arthropod species. Since they often induce a cytoplasmic mating incompatibility (CI) in their hosts that acts as a postzygotic isolating mechanism between differently infected individuals of one species, Wolbachia have received attention as a potential promoter of arthropod speciation processes. Previous studies on speciation focused on either Wolbachia-induced or the classical nuclear-based postzygotic isolating mechanism. However, it should usually be the case that both co-occur. This thesis continues investigations on Wolbachia''s role in speciation by analyzing interactions of Wolbachia-induced CI and nuclear incompatibility (NI) caused by genetic differentiation. We will show that Wolbachia have strong impact on nuclear-based speciation processes. In particular, synergy effects can occur when both isolating mechanisms act simultaneously. Furthermore, we show that Wolbachia can influence speciation processes under more general conditions than previous studies on Wolbachia''s role in speciation suggested. Since the actual role of Wolbachia in arthropod speciation will strongly depend on their abundance, we present a statistical meta-analysis of published data on Wolbachia infection frequencies. Due to the sampling methods applied in studies on Wolbachia infection frequencies, it is likely that current estimates of 20% infected species are underestimates. This is supported by our analysis and we show that more likely about two-thirds of species are infected. Combining both results, this thesis provides strong evidence for Wolbachia being a very general factor in arthropod speciation processes.