Basic Glossary on Genetic Epidemiology

This is the second of a series of three glossaries on genetic concepts used in epidemiological research that the journal is publishing with the objective of helping the reader “walk” around the journal.

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Basic Glossary on Genetic Epidemiology

  • EPISTASIS
    Gene interaction and, particularly, interaction between different alleles at different genes. Epistasis can occur at the same step or at different stages of the same biochemical pathway.
    The first glossary, on basic molecular genetic terms,1 provided the basis to understand the concepts presented here. In this section, we refer to the most basic and commonly used genetic terms that epidemiologists interested in this kind of research need to know. The concepts defined here are the pillars on which genetic epidemiology builds up its methodology. Again, the list is not exhaustive and an attempt has been made to provide you with concise definitions. Hence, we encourage the interested reader to further \”explore\” the classic bibliography on genetics and genetic epidemiology2-5 to complete their knowledge on this topic.
  • FAMILIAL AGGREGATION
    A tendency of a disease to cluster in families, which is generally taken as evidence for the existence of a genetic aetiological mechanism, or environmental factors common to family members, or a combination of both. Ascertainment bias should be seriously considered.
  • FAMILIAL ANTICIPATION
    The younger age of appearance of a late onset trait in successive generations. A typical effect in repeat expansions, in which severity of the disease is proportional to repeat length, which tends to grow in each transmission.
  • CANDIDATE GENE
    A known gene suspected to be associated with the disease of interest on the basis of the biological function of its protein.
  • FOUNDER EFFECT
    A change in the population allele frequency that occurs when a subpopulation is established by a small number of individuals. The change occurs only by chance because the members of the new population are a random subsample that may deviate from the overall allele frequencies. Such changes are stronger in smaller founder populations, given the higher sampling variance.
  • COMPLEX TRAIT (POLYGENIC TRAIT, MULTIFACTORIAL TRAIT)
    Any phenotype that results from the effect of multiple genes at two or more loci, with possible environmental influences too. Examples are: obesity, hypertension, hypercholesterolaemia, skin pigmentation, cancer, etc. Discontinuous trait Trait that is either present or absent, such as birth defects and common behavioural disorders. The threshold model is used to explain discontinuous traits: a protein level has a continuous distribution but the phenotype does not appear until a certain threshold is reached. Continuous trait Measurable trait that is always present and that follows a normal distribution in the population. For example: height, weight, and blood pressure.
  • GENETIC HETEROGENEITY
    Process by which a phenotype can be caused by different loci. A complex example is epilepsy, which may be attributable to different causes in different individuals: single gene disorders, multifactorial inheritance, chromosomal disorders, or even brain injuries. The last case is a phenocopy.
  • GENOTYPE
    The genetic constitution of an organism, which is modulated by the environment before being expressed as a phenotype.
  • CO-SEGREGATION
    The tendency of two traits to be jointly inherited.
  • HAPLOTYPE
    Set of allelic states found at neighbouring loci in a chromosome, as inherited from a parent. Haplotypes can be broken down by recombination. A haplotype shared among unrelated individuals affected with a genetic disease may indicate that a gene causing the disease maps to that genomic region.
  • DNA REPAIR
    Major cell defence system against DNA damage produced by environmental and endogenous compounds. There are several different repair
    HARDY-WEINBERG EQUILIBRIUM
    State in which the allele and genotype frequencies do not change from one generation to the next in a population. It requires random mating and the absence of selection, mutation, migration, and genetic drift. In Hardy-Weinberg equilibrium, allele and genotype frequencies are related through the Hardy-Weinberg law: for a locus with two alleles P, Q at frequencies p and q respectively, homozygotes for P are found at frequency p2, homozygotes for Q have a frequency q2, and heterozygotes are found at a frequency 2pq. Although conditions for Hardy-Weinberg equilibrium are seldom strictly met, genotype frequencies are usually consistent with the HardyWeinberg law. Some useful software packages to test whether a set of genotypic frequencies conforms to Hardy-Weinberg are Arlequin (http://anthropologie.unige.ch/arlequin/) and Genepop (http://wbiomed.curtin.edu.au/genepop/), among others.
  • LINKAGE
    The phenomenon whereby phenotypes and alleles at one or more marker alleles tend to be inherited together more often than expected. Linkage usually means that a gene contributing partially or completely to the phenotype (a genetic disease, for instance) maps in the vicinity of the markers.
  • MARKER
    Any neutral polymorphism used in linkage or association analysis.
  • MEIOSIS
    Process whereby four haploid germ cells (gametes) are produced from a diploid parent cell for sexual reproduction. During meiosis crossovers occur between homologous chromosomes so that each chromosome found in the gamete consists of a patchwork of material from both members of the pair.
  • INHERITANCE
    Pattern followed by the transmission from generation to generation of a given phenotype, usually a disease. Complex inheritance (non-Mendelian inheritance) Variability in phenotype expression that is attributed both to the inheritance of combinations of alleles at multiple loci and to environment exposures.
  • METABOLISM (OF EXOGENOUS AND ENDOGENOUS CHEMICAL COMPOUNDS)
    Cellular system of enzymes (most of them polymorphic) that activates and deactivates chemical compounds through chemical radicals. Metabolic enzymes are classified in two groups according their most important function, activating or deactivating, and in several families.
    Multifactorial inheritance
    Complex inheritance in which multiple genes are involved jointly with environmental influences.
  • MITOSIS
    Asexual reproduction of a somatic cell in which the two daughter cells each have a genetic makeup that is identical to that of the parent cell.
    Polygenic inheritance
    Complex inheritance in which multiple genes but no environmental factors are involved. Mendelian inheritance Simple pattern of inheritance that follows the rules set out by Mendel. Mendelian traits are determined by just one genetic locus, with complete penetrance and no phenocopies. Mendelian inheritance can be dominant, recessive, or sex linked.
  • PENETRANCE
    The likelihood, or probability, that a particular genotype will be expressed in the phenotype. A penetrance of 100% means that the associated phenotype always occurs when the corresponding genotype is present. Similarly, if only 30% of those carrying a particular allele (such as a disease-causing mutation) exhibit a phenotype (the disease), the penetrance is 30%.
    Dominant inheritance
    Type of inheritance in which one copy of an abnormal gene is sufficient to cause disease (for example, Huntington\’s disease). If penetrance is complete, the abnormal gene is inherited from a parent who also has the disorder and every generation in the family has members with the disorder.
  • PHENOCOPY
    An environmentally caused phenotype that mimics a genetic trait. For example, epilepsy can be caused by mutations in single genes (with genetic heterogeneity), and, among other causes, by brain injury, which produces a phenocopy of genetic epilepsy.
    Recessive inheritance
    Type of inheritance in which two abnormal copies of the gene must be present for the individual to be affected (for example, cystic fibrosis). Each parent contributes one abnormal copy of the gene to the child who has the disorder. Heterozygous individuals (such as the parents of the affected) are called carriers of the disorder because they have one normal and one abnormal copy of the gene, but they do not show symptoms of the disorder.
  • PHENOTYPE
    Expressed traits or characteristics of an organism, regardless of whether or to what extent the traits are the result of genotype or environment, or of the interaction of both. For example, hair colour, weight, or the presence or absence of a disease.
Download Basic Glossary on Genetic Epidemiology pdf from www.ncbi.nlm.nih.gov, 3 pages, 81.82KB.
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