Trait phenotypic

The Human Genome Project extended the reach of research still further, with genome-wide association (GWA) studies. These studies examine common genetic variants that occur across the human genome to identify associations with observable disease traits (phenotypes). 

A co-dominant is a heritable trait in which both alleles of a polymoiphism are expressed and are reflected in the phenotype. The phenotype of heterozygous carriers is in between the phenotypes of the two homozygous genotypes. 

Phenotype is the actual appearance of an organism or, more specifically in the research context, of a trait of interest. It may be a binary trait, i.e., the presence/ absence of a disease, for example essential hypertension, or a quantitative trait, such as blood pressure level. 

Mutations in human Kv-channel genes have been detected that are associated with hereditary diseases ranging from heart arrythmia (long QT-syndrome) and deafness to epilepsy and ataxia (see Table 2). Typically, many Kv-channel related channelopathies are correlated with a mutant phenotype that is episodic in nature and appears as a dominant hereditary trait. 

In summary, the life cycle of S. ratti contains a switch between two developmental routes. The developmental propensity phenotype varies between different isofemale lines and this can be altered by artificial selection. This shows that there is diversity for this trait both within and between parasite... 

Taken as a whole, these observations show that parasite lines differ in an immune-dependent manner in their infection/expulsion kinetics. Furthermore, there is heritable variation in survival and fecundity in previously exposed hosts and quantitative variation in the immune response that selected parasite lines elicit. Again, taken as a whole, these observations have the necessary corollary that variation in these traits exists not only in laboratory-maintained isolates but also in helminth species in nature. The phenotypes under consideration here (infection/expulsion kinetics, survival, fecundity) are multifactorial life-history traits. Understanding the basis of variation in the components and interplay of these complex, immune-responsive phenotypes must be of crucial relevance to understanding the immunology of infections of parasitic nematodes. This is of particular relevance in view of current attempts to develop immunological methods of nematode control. 

Of the examples considered above, two are of phenotypic diversity in a life-history trait where the life-history trait under consideration is clearly a facultative phenomenon. That is, for developmental route in S. ratti and for arrested development, there are distinct, mutually exclusive developmental routes. Thus, diversity in these traits between different parasite lines is relatively easy to observe, as is the response to selection. Both these traits are, in part, affected by environmental conditions and so are phenotypically plastic. For S. ratti, variation in the sensitivity of this plasticity can also be seen. Although environmental sensitivity of arrested development is as yet uninvestigated, by analogy with S. ratti it is likely to vary. 

The third example considered the interaction of life-history traits (survival rates, fecundity, immunogenicity) with an environmental factor specific to parasites, namely the host immune system. Here phenotypic diversity in response to environmental conditions (host immunity) is not so readily apparent. To observe phenotypic diversity, different parasite lines need to be compared in their kinetics of infection and, to show immune-dependence, these must be complemented by control experiments in immunosuppressed hosts. Experiments seeking to select on this diversity... 

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