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Incomplete lineage sorting (ILS) (also referred to as hemiplasy, deep coalescence , retention of ancestral polymorphism , or trans-species polymorphism) is a phenomenon in evolutionary biology and population genetics that results in discordance between species and gene trees . By contrast, complete lineage sorting results in concordant species and gene trees. ILS occurs in the context of a gene in an ancestral species which exists in multiple alleles. If a speciation event occurs in this situation, either complete lineage sorting will occur, and both daughter species will inherit all alleles of the gene in question, or incomplete lineage sorting will occur, when one or both daughter species inherits a subset of alleles present in the parental species. For example, if two alleles of a gene are present and a speciation event occurs, one of the two daughter species might inherit both alleles, but the second daughter species only inherits one of the two alleles. In this case, incomplete lineage sorting has occurred.

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25-399: Bos is a genus of domestic cattle. Bos , BOS or BoS may also refer to: Bos See § Species . Bos (from Latin bōs : cow , ox , bull ) is a genus of bovines , which includes, among others, wild and domestic cattle. Bos is often divided into four subgenera : Bos , Bibos , Novibos , and Poephagus , but including these last three divisions within

50-414: A 9–11 month gestation , depending on the species and birth one or, rarely, two young in the spring. Most species travel in small herds ranging in size from ten to thirty members. Within most herds, there is one bull (male) for all the cows (female). Dominance is important in the herds; calves will usually inherit their mother's position in the hierarchy . They are generally diurnal , resting in

75-474: A phylogenetic analysis of one or two genes from the strains from the accused and the victim have been used to infer transmission; however, the commonality of incomplete lineage sorting means that transmission cannot be inferred solely on the basis of such a basic analysis. Jacques and List (2019) show that the concept of incomplete lineage sorting can be applied to account for non-treelike phenomena in language evolution. Kalyan and François (2019), proponents of

100-507: A single gene, it can have multiple versions ( alleles ) causing different characters to appear (polymorphisms). In the example shown in Figure 1, the gene G has two versions (alleles), G0 and G1. The ancestor of A, B and C originally had only one version of gene G, G0. At some point, a mutation occurred and the ancestral population became polymorphic, with some individuals having G0 and others G1. When species A split off, it retained only G1, while

125-470: Is a common feature in viral phylodynamics , where the phylogeny represented by transmission of a disease from one person to the next, which is to say the population level tree, often doesn't correspond to the tree created from a genetic analysis due to the population bottlenecks that are an inherent feature of viral transmission of disease. Figure 3 illustrates how this can occur. This has relevance to criminal transmission of HIV where in some criminal cases,

150-610: Is not caused by incomplete lineage sorting. Incomplete lineage sorting has important implications for phylogenetic research. There is a chance that when creating a phylogenetic tree it may not resemble actual relationships because of this incomplete lineage sorting. However, gene flow between lineages by hybridization or horizontal gene transfer may produce the same conflicting phylogenetic tree. Distinguishing these different processes may seem difficult, but much research and different statistical approaches are (being) developed to gain greater insight in these evolutionary dynamics. One of

175-449: Is used to diagram hominin lineages that may have failed to sort out at the same time that speciation occurred in prehistory. Due to the advent of genetic testing and genome sequencing, researchers found that the genetic relationships between hominin lineages might disagree with previous understandings of their relatedness based on physical characteristics. Moreover, divergence of the last common ancestor (LCA) may not necessarily occur at

200-516: The ancestor of A, B and C, and the ancestor of B and C, had only the G0 version of gene G. A mutation occurred at the divergence of B and C, and B acquired a mutated version, G1. Some time later, the arrow shows that G1 was transferred from B to A by some means (e.g. hybridization or horizontal gene transfer). Studying only the final states of G in the three species makes it appear that A and B are sisters rather than B and C, as in Figure 1, but in Figure 2 this

225-426: The ancestor of B and C remained polymorphic. When B and C diverged, B retained only G1 and C only G0; neither were now polymorphic in G. The tree for gene G shows A and B as sisters, whereas the species tree shows B and C as sisters. If the phylogeny of these species is based on gene G, it will not represent the actual relationships between the species. In other words, the most related species will not necessarily inherit

250-411: The bonobo genome, sequences are more closely related to homologues of humans than to chimpanzees, which is probably a result of incomplete lineage sorting. A study of more than 23,000 DNA sequence alignments in the family Hominidae (great apes, including humans) showed that about 23% did not support the known sister relationship of chimpanzees and humans. In human evolution, incomplete lineage sorting

275-522: The bonobo-chimpanzee ancestor and humans, indicating that humans and chimpanzees shared a common ancestor for several million years after separation from gorillas. This creates the phenomenon that is incomplete lineage sorting. Today researchers are relying on DNA fragments in order to study the evolutionary relationships among humans and their counterparts in the hope that it will provide information about speciation and ancestral processes from genomes from different types of humans. Incomplete lineage sorting

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300-462: The common species are to be named Bos primigenius and Bos gaurus . During the 2010s, analysis of the complex genetics of the bovine lineages determined that the genus Bison needed to be relegated to a subgenus of Bos in order to retain monophyly within Bos since both extant species of Bison are phylogenetically embedded within Bos . The specific relationships in these analyses determined that

325-408: The extinct aurochs . Others like Bali cattle and gayal are thought to have originated from South and Southeast Asian Bos species. The species are grazers, with large teeth to break up the plant material they ingest. They are ruminants , having a four-chambered stomach that allows them to break down plant material. There are about 1.3 billion domestic cattle alive today, making them one of

350-509: The gene tree consists of other pre-existing lineages. If the population is bigger these ancestral lineages are going to persist longer. When you get large ancestral populations together with closely timed speciation events these different pieces of DNA retain conflicting affiliations. This makes it hard to determine a common ancestor or points of branching. When studying primates, chimpanzees and bonobos are more related to each other than any other taxa and are thus sister taxa . Still, for 1.6% of

375-491: The genus Bos without including Bison is believed to be paraphyletic by many workers on the classification of the genus since the 1980s. The genus as traditionally defined has five extant species, but this rises to eight when the domesticated varieties are counted as separate species, and ten when the closely related Bison is also included. Most but not all modern breeds of domesticated cattle (including taurine cattle and zebu ) are believed to have originated from

400-549: The hot part of the day and being active morning and afternoon. In areas where humans have encroached on the territory of a herd, they may turn nocturnal . Some species are also migratory, moving with food and water availability. In 2003, the International Commission on Zoological Nomenclature resolved a long-standing dispute about the naming of those species (or pairs of species) of Bos that contain both wild and domesticated forms. The commission "conserved

425-1034: The mitochondrial DNA of the American bison and wisent is suggested to be likely due to incomplete lineage sorting or genetic introgression into B. bonasus from other Bos species. Relationships of members of the genus Bos based on nuclear genomes after Sinding, et al. 2021. Bos primigenius + Bos taurus (aurochs and cattle) Bos mutus (wild yak) Bison bison (American bison) Bison bonasus (European bison/wisent) Bos javanicus (banteng) Bos gaurus (gaur) Bos sauveli (kouprey) The following species are known: Incomplete lineage sorting The concept of incomplete lineage sorting has some important implications for phylogenetic techniques. The persistence of polymorphisms across different speciation events can cause incomplete lineage sorting. Suppose two subsequent speciation events occur where an ancestor species gives rise firstly to species A, and secondly to species B and C. When studying

450-420: The most related genes. This is of course a simplified example of incomplete lineage sorting, and in real research it is usually more complex containing more genes and species. However, other mechanisms can lead to the same apparent discordancy, for example, alleles can move across species boundaries via hybridization, and DNA can be transferred between species by viruses. This is illustrated in Figure 2. Here

475-442: The other great apes from the hominin lineage. Incomplete lineage sorting means that the average divergence time between genes may differ from the divergence time between species. Models suggest that the average divergence time between the genes in the human and chimpanzee genome is older than the split between humans and gorillas. What this means is the common ancestor of humans and chimpanzees has left traces of genetic material that

500-452: The resolutions to reduce the implications of incomplete lineage sorting is to use multiple genes for creating species or population phylogenies. The more genes used, the more reliable the phylogeny becomes. Incomplete lineage sorting commonly happens with sexual reproduction because the species cannot be traced back to a single person or breeding pair. When organism tribe populations are large (i.e. thousands) each gene has some diversity and

525-436: The same time as speciation. Lineage sorting is a method that allows paleoanthropologists to explore the genetic relationships and divergences that may not fit with their previous speciation models based on phylogeny alone. Incomplete lineage sorting of the human family tree is an area of great interest. There are a number of unknowns when considering both the transition from archaic humans to modern humans and divergence of

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550-432: The two living bison species were each other's closest living relatives, with their closest relatives amongst Bos being the yaks based on nuclear DNA . The mitochondrial DNA for the wisent was found to contradict the nuclear DNA result, and was more closely related to those of cattle, while the mitochondrial DNA of the American bison supported the nuclear DNA result of a close relationship with yaks. The discrepancy between

575-408: The usage of 17 specific names based on wild species, which are pre-dated by or contemporary with those based on domestic forms", confirming Bos primigenius for the aurochs and Bos gaurus for the gaur. If domesticated cattle and gayal are considered separate species, they are to be named Bos taurus and Bos frontalis ; however, if they are considered part of the same species as their wild relatives,

600-538: The world's most numerous mammals. Members of this genus are currently found in Africa, Asia, Europe, parts of North America, South America and also in Oceania. Their habitats vary greatly depending on the particular species; they can be found in prairies, rain forests, wetlands, savannah and temperate forests. Most Bos species have a lifespan of 18–25 years in the wild, with up to 36 being recorded in captivity. They have

625-410: Was present in the common ancestor of humans, chimpanzees, and gorillas. However, the genetic tree slightly differs from that of the species or phylogeny tree. In the phylogeny tree when we look at the evolutionary relationship between the human, bonobo chimpanzee, and gorilla, the results show that the separation of bonobo and chimpanzee transpired in a close proximity of time to the common ancestor of

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