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Cultural hitchhiking is a hypothesized gene-culture coevolutionary process through which cultural selection, sexual selection based on cultural preference, limits the diversity at genetically neutral loci being transmitted in parallel to selective cultural traits. The process is thought to account for exceptionally low diversity in neutral loci such as control regions of the mitochondrial genome unaccounted for by any other selective forces. Simply put, selection for certain learned social and cultural behaviors can manifest in specific shaping of a population’s genetic makeup. While the notion that culture plays a significant role in shaping community genetics is widely accepted in the context of human populations it had not been considered or documented in non-human organisms until the late 1990s. The term was coined by the cetologist Hal Whitehead who studies the cultures and population genetics of matrilineal whale communities.
Cultural hitchhiking has been proposed as a cause for reduced genetic diversity at certain loci in prehistoric Homo sapiens , dolphins, killer whales, and sperm whales. [1]
Cultural hitchhiking is a significant hypothesis because it investigates the relationship between population genetics and culture. By understanding how social behavior can shape the genetic makeup of communities scientists are better able to explain why certain communities have genetic traits distinct from the larger population.
The process was initially proposed by Whitehead in a 1998 paper as an explanation for the low genetic diversity in matrilineal whale species. In these communities, female individuals remain grouped together with their mothers and other female relatives. [2] They appear to select mates from outside their immediate community based on culturally valued social traits and aptitude. Sequencing of the mitochondrial genome of individuals within these communities revealed them to have a significantly reduced diversity in certain control loci compared to comparable panmictic populations. Whitehead discovered that the relative frequency of mitochondrial haplotypes characteristic of groups exhibiting more highly adaptive socially learned traits would increase, while the frequency of these haplotypes in groups with less adaptive socially learned traits would decrease. This coincidental selective pressure is thought to have led to an overall reduction in haplotype diversity across the entire species population.
In 2014 a team of biologists from the University of South Wales attributed a remarkable geographic distribution of mitochondrial haplotypes among adjacent populations of bottlenose dolphins in a bay in Western Australia to cultural hitchhiking. [3] [4] The researchers found Whitehead’s hypothesis that selection for learned social traits affected diversity in neutral gene loci fit well with their observations. It was discovered that dolphins with two of three mitochondrial haplotypes were found predominantly in water deeper than 10 m while those with the third haplotypes were found predominantly in depths less than 10 m. This geographic distinction between these populations is also associated with different learned behaviors. Some of the dolphins predominantly found in deeper waters exhibit foraging strategies that implement tools such as a sponge placed on their beak. This "sponging" behavior is found to be spread through vertical social transmission along a matrilineal pattern (i.e. the mothers teach the behavior to their offspring). All dolphins exhibiting one of the deepwater haplotypes belong to a single matriline. The researchers ultimately concluded that these fine-scale genetic structures, the distinct mitochondrial haplotypes, have probably arisen based on socially transmitted behaviors or in other words, through cultural hitchhiking. A study in the same area and species showed that shelling is also marginally learned from associates. [5]
Cultural hitchhiking has been proposed as an explanation for a widely inferred and abrupt Y-chromosome population bottleneck across several Old World (Africa, Europe, Asia) populations around 4000-6000 BC. This bottleneck is thought to suggest a significant decline in the effective male population during Neolithic times to an estimated 1/20th its original size. Though mitochondrial sequence records seem to indicate uninhibited population increase at this time meaning there was likely an extreme divergence in the size of male and female effective population sizes during the bottleneck period. A team of international genetics, archaeology, and anthropology researchers in a 2018 article hypothesized that the bottleneck was a consequence of intergroup competition between patrilineal kin groups, which caused cultural hitchhiking between Y-chromosomes and cultural groups and reduction in Y-chromosomal diversity. [6] The authors Zeng et al. argue that competition between patrilineal kin communities produces two mechanisms with limiting effect on Y-chromosome diversity. One mechanism being these patrilineal groups by virtue of common descent produce elevated levels of Y-chromosome homogeneity and high inter-group diversity. The second mechanism is violent inter-group competition which disproportionately results in male group member casualties and therefore concentration of like y-chronotypes and in some cases extinction complete extinction of entire lineages.
In human genetics, the Mitochondrial Eve is the matrilineal most recent common ancestor (MRCA) of all living humans. In other words, she is defined as the most recent woman from whom all living humans descend in an unbroken line purely through their mothers and through the mothers of those mothers, back until all lines converge on one woman.
A population bottleneck or genetic bottleneck is a sharp reduction in the size of a population due to environmental events such as famines, earthquakes, floods, fires, disease, and droughts; or human activities such as genocide, speciocide, widespread violence or intentional culling. Such events can reduce the variation in the gene pool of a population; thereafter, a smaller population, with a smaller genetic diversity, remains to pass on genes to future generations of offspring. Genetic diversity remains lower, increasing only when gene flow from another population occurs or very slowly increasing with time as random mutations occur. This results in a reduction in the robustness of the population and in its ability to adapt to and survive selecting environmental changes, such as climate change or a shift in available resources. Alternatively, if survivors of the bottleneck are the individuals with the greatest genetic fitness, the frequency of the fitter genes within the gene pool is increased, while the pool itself is reduced.
In human genetics, the Y-chromosomal most recent common ancestor is the patrilineal most recent common ancestor (MRCA) from whom all currently living humans are descended. He is the most recent male from whom all living humans are descended through an unbroken line of their male ancestors. The term Y-MRCA reflects the fact that the Y chromosomes of all currently living human males are directly derived from the Y chromosome of this remote ancestor. The analogous concept of the matrilineal most recent common ancestor is known as "Mitochondrial Eve", the most recent woman from whom all living humans are descended matrilineally. As with "Mitochondrial Eve", the title of "Y-chromosomal Adam" is not permanently fixed to a single individual, but can advance over the course of human history as paternal lineages become extinct.
Y-chromosomal Aaron is the name given to the hypothesized most recent common ancestor of the patrilineal Jewish priestly caste known as Kohanim. According to the traditional understanding of the Hebrew Bible, this ancestor was Aaron, the brother of Moses.
A haplotype is a group of alleles in an organism that are inherited together from a single parent.
In biology and genetic genealogy, the most recent common ancestor (MRCA), also known as the last common ancestor (LCA), of a set of organisms is the most recent individual from which all the organisms of the set are descended. The term is also used in reference to the ancestry of groups of genes (haplotypes) rather than organisms.
A genealogical DNA test is a DNA-based genetic test used in genetic genealogy that looks at specific locations of a person's genome in order to find or verify ancestral genealogical relationships, or to estimate the ethnic mixture of an individual. Since different testing companies use different ethnic reference groups and different matching algorithms, ethnicity estimates for an individual vary between tests, sometimes dramatically.
A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplotype is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual.
Human genetic variation is the genetic differences in and among populations. There may be multiple variants of any given gene in the human population (alleles), a situation called polymorphism.
The genetic history of Europe includes information around the formation, ethnogenesis, and other DNA-specific information about populations indigenous, or living in Europe.
Animal culture can be defined as the ability of non-human animals to learn and transmit behaviors through processes of social or cultural learning. Culture is increasingly seen as a process, involving the social transmittance of behavior among peers and between generations. It can involve the transmission of novel behaviors or regional variations that are independent of genetic or ecological factors.
Haplogroup T-M184, also known as Haplogroup T, is a human Y-chromosome DNA haplogroup. The unique-event polymorphism that defines this clade is the single-nucleotide polymorphism known as M184.
Haplogroup BT M91, also known as Haplogroup A1b2, is a Y-chromosome haplogroup. BT is a subclade of haplogroup A1b (P108) and a sibling of the haplogroup A1b1 (L419/PF712).
Haplotype convergence is the unrelated appearance of identical haplotypes in separate populations, through either convergent evolution or random chance.
The tables below provide statistics on the human Y-chromosome DNA haplogroups most commonly found among ethnolinguistic groups and populations from East and South-East Asia.
The Y Chromosome Haplotype Reference Database (YHRD) is an open-access, annotated collection of population samples typed for Y chromosomal sequence variants. Two important objectives are pursued: (1) the generation of reliable frequency estimates for Y-STR haplotypes and Y-SNP haplotypes to be used in the quantitative assessment of matches in forensic and kinship cases and (2) the characterization of male lineages to draw conclusions about the origins and history of human populations. The database is endorsed by the International Society for Forensic Genetics (ISFG). By May 2023 about 350,000 Y chromosomes typed for 9-29 STR loci have been directly submitted by worldwide forensic institutions and universities. In geographic terms, about 53% of the YHRD samples stem from Asia, 21% from Europe, 12% from North America, 10% from Latin America, 3% from Africa, 0.8% from Oceania/Australia and 0.2% from the Arctic. The 1.406 individual sampling projects are described in more than 800 peer-reviewed publications
The relationship of the Mayas to other indigenous peoples of the Americas has been assessed using traditional genetic markers. Mayas inhabited several parts of Mexico and Central America, including Chiapas, the northern lowlands of the Yucatán Peninsula, the southern lowlands and highlands of Guatemala, Belize, and parts of western El Salvador and Honduras. Genetic studies of the Maya people are reported to show higher levels of variation when compared to other groups.
Haplogroup T-L206, also known as haplogroup T1, is a human Y-chromosome DNA haplogroup. The SNP that defines the T1 clade is L206. The haplogroup is one of two primary branches of T (T-M184), the other subclade being T2 (T-PH110).
This glossary of genetics and evolutionary biology is a list of definitions of terms and concepts used in the study of genetics and evolutionary biology, as well as sub-disciplines and related fields, with an emphasis on classical genetics, quantitative genetics, population biology, phylogenetics, speciation, and systematics. It has been designed as a companion to Glossary of cellular and molecular biology, which contains many overlapping and related terms; other related glossaries include Glossary of biology and Glossary of ecology.