Person: Haig, David
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Haig
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Haig, David
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Publication Response to vocal music in Angelman syndrome contrasts with Prader-Willi syndrome(Center for Open Science, 2018-08-13) Kotler, Jennifer; Mehr, Samuel; Egner, Alena; Haig, David; Krasnow, MaxParent-offspring conflict, or the conflict over resources between parents and their children due to differences in genetic relatedness, is the biological foundation for a variety of psychological phenomena, including sibling rivalry and child abuse. This form of conflict is particularly relevant to the domain of parental investment: the provisioning of resources to offspring by parents and alloparents. The kinship theory of genomic imprinting is the primary evolutionary explanation for the occurrence of specialized genetic expression in chromosomal domains relevant to phenotypic expression of parent-offspring conflict. Specifically, complementary parental contributions in the same region of the genome promote opposing parental demand behaviors. This theory predicts that people with genomic imprinting disorders will show alterations in traits and behaviors related to parental investment. In this paper, we apply this prediction to the psychological resource of parental attention, for which vocalizations in general, and music in particular, may be an honest signal. Individuals with Prader-Willi syndrome show increased physiological responses to music listening consistent with a reduced demand for parental investment. Here we report the complementary pattern necessary to support the theory: we find that individuals with Angelman syndrome demonstrate a relatively reduced physiological response to music, consistent with an increased demand for parental investment. In addition to presenting evidence of the value of applying the kinship theory of genomic imprinting to psychological phenomena, these data provide a comprehensive test of the theory that at least one aspect of human musical psychology evolved to mediate conflict over attentional demands between parents and offspring.Publication Poles Apart: Monosporic, Bisporic, and Tetrasporic Embryo Sacs Revisited(Frontiers Media SA, 2020-09-15) Haig, DavidBisporic embryo sacs contain nuclei derived from two members of a megaspore tetrad whereas tetrasporic embryo sacs contain nuclei derived from all four members of a tetrad. Megaspores from the same tetrad are less genetically similar than are megaspores from different tetrads. Therefore, cells derived from different megaspores in bisporic and tetrasporic embryo sacs are expected to compete with each other rather than cooperate. The tacit assumption of the plant embryological literature that bisporic and tetrasporic embryo sacs function as integrated organisms is demonstrably false, both theoretically and empirically. This competition within embryo sacs can be expressed as the formation of eggs by descendants of more than one megaspore or by the suppression of the descendants of all but one megaspore. Both phenomena have evolved multiple times. In contrast, all nuclei of monosporic female gametophytes are genetically identical. Consequently, monosporic development is predicted to be more evolutionarily stable than bisporic or tetrasporic development. The triploid endosperm produced by most monosporic gametophytes was probably derived from an ancestrally diploid endosperm and has been considered a key adaptation of the most successful lineages of flowering plants. The greater weight given to the doubled maternal genome in triploid endosperm may have facilitated a more efficient distribution of resources among a mother’s seeds because it reduced the influence of competition for maternal resources among unrelated paternal genomes of endosperm.Publication Coadaptation and conflict, misconception and muddle, in the evolution of genomic imprinting(Nature Publishing Group, 2013) Haig, DavidCommon misconceptions of the ‘parental conflict’ theory of genomic imprinting are addressed. Contrary to widespread belief, the theory defines conditions for cooperation as well as conflict in mother–offspring relations. Moreover, conflict between genes of maternal and paternal origin is not the same as conflict between mothers and fathers. In theory, imprinting can evolve either because genes of maternal and paternal origin have divergent interests or because offspring benefit from a phenotypic match, or mismatch, to one or other parent. The latter class of models usually require maintenance of polymorphism at imprinted loci for the maintenance of imprinted expression. The conflict hypothesis does not require maintenance of polymorphism and is therefore a more plausible explanation of evolutionarily conserved imprinting.Publication Genetic dissent and individual compromise(Springer Science + Business Media, 2014) Haig, DavidOrganisms can be treated as optimizers when there is consensus among their genes about what is best to be done, but genomic consensus is often lacking, especially in interactions among kin because kin share some genes but not others. Grafen adopts a majoritarian perspective in which an individual’s interests are identified with the interests of the largest coreplicon of its genome, but genomic imprinting and recombination factionalize the genome so that no faction may predominate in some interactions among kin. Once intragenomic conflicts are recognized, the individual organism can be conceptualized as an arbiter among competing interests within a collective. Organismal adaptation can be recognized without phenotypes being optimized.Publication Review of "Sex Itself: The Search for Male and Female in the Human Genome."(University of Chicago Press, 2014) Haig, DavidPublication Fighting the good cause: meaning, purpose, difference, and choice(Springer Science + Business Media, 2014) Haig, DavidConcepts of cause, choice, and information are closely related. A cause is a choice that can be held responsible. It is a difference that makes a difference. Information about past causes and their effects is a valuable commodity because it can be used to guide future choices. Information about criteria of choice is generated by choosing a subset from an ensemble for ‘reasons’ and has meaning for an interpreter when it is used to achieve an end. Natural selection evolves interpreters with ends. Surviving genes embody a textual record of past choices that had favorable outcomes. Consultation of these archives guides current choices. Purposive choice is well-informed difference making.Publication Specialists and Generalists: The Sexual Ecology of the Genome(Cold Spring Harbor Laboratory Press, 2014) Haig, David; Ubeda, F.; Patten, M. M.Sexual antagonism occurs when an allele is beneficial in one sex but costly in the other. Parental antagonism occurs when an allele is beneficial when inherited from one sex but costly when inherited from the other because of fitness interactions among kin. Sexual and parental antagonisms together define four genetic niches within the genome that favor different patterns of gene expression. Natural selection generates linkage disequilibrium among sexually and parentally antagonistic loci with male-beneficial alleles coupled to alleles that are beneficial when inherited from males and female-beneficial alleles coupled to alleles that are beneficial when inherited from females. Linkage disequilibrium also develops between sexually and parentally antagonistic loci and loci that influence sex determination. Genes evolve sex-specific expression to resolve sexual antagonism and evolve imprinted expression to resolve parental antagonism. Sex-specific chromosomes allow a gene to specialize in a single niche.Publication Sexual Selection: Placentation, Superfetation, and Coercive Copulation(Elsevier BV, 2014) Haig, DavidThe evolution of placentas in poeciliid fishes is associated with conception of overlapping litters and male mating strategies becoming more coercive. Sperm competition in ovaries of multiply-inseminated females may favor fertilization of immature eggs during ongoing pregnancies.Publication Does microchimerism mediate kin conflicts?(Informa UK Limited, 2014) Haig, DavidFetal microchimerism (FMc) is predicted to promote the fitness of the fetus and maternal microchimerism (MMc) to promote the fitness of the mother. Offspring and mothers benefit from each other’s health. Therefore, microchimeric cells should usually not be harmful to their host. However, the evolutionary interests of mothers and offspring diverge when there is competition among siblings for maternal investment. Fetal cells in mothers’ bodies could benefit their own offspring at the expense of its sibs by promoting lactogenesis or by extending the interbirth interval. Maternal cells in fetal bodies could benefit from the suppression of sibling rivalry. Non-inherited haplotypes in MMc or sibling microchimerism (SMc) gain no direct benefit from their hosts’ health and could be associated with substantial detrimental effects.Publication Imprinted green beards: a little less than kin and more than kind(The Royal Society, 2013) Haig, DavidRNA is complementary to the DNA sequence from which it is transcribed. Therefore, interactions between DNA and RNA provide a simple mechanism of genetic self-detection within nuclei. Imprinted RNAs could enable alleles of maternal and paternal origin to detect whether they are the same (homozygous) or different (heterozygous), and thereby provide strategic information about expected relatedness to siblings.