Dancing David
Penultimate Amazing
In this case, saying "partial" and "full-blown" is both misleading and unscientific. (not terms used anywhere on the wiki pages on this, for example) Also the analogy to depression is improper, there is no parallel in genetics or heritability, this is a condition ubiquitous to age and race. Finally, it's not "full trait", it's developing the disease. We can tell the trait works for a purpose and the disease is an occasional unwanted result. Obviously, many more people have the protective trait than develop the disease. So the fact that this mutation sometimes leads to disease is just a cost that is outweighed by the benefit. When there is no more malaria, the disease starts to disappear, it's a complete picture.
So, depression evolved as a function, and can become disordered for a multitude of reasons, but like sickle-cell, there is nothing "partial" or "not directly selected for" about it.
Yo are correct I did not parse exact language and my usage is confusing:
http://en.wikipedia.org/wiki/Heterozygote_advantage
in the case of sickle cell disease the benefit comes more from the presentation of the individual who are carriers of the single gene set (heterozygous) as opposed to those who have the complimentary gene (homozygous)
So again in this case of sickle cell those who have the (in my faulty language) partial trait (heterozygous) are likely have a benefit in reproduction due to the the protective effects vs. the detriment, but those who have the (in my faulty language) full trait (homozygous) are likely to have a detriment in reproduction due to increased mortality.
So in depression if we have an even more complex set of genetic factors (which is likely given the multiple pathways currently suggested) then for an individual who has a very high chance of endogenous major depression they are (in my thought) more likely to have a greater preponderance of the expression of those genetic factors. Now it is very likely to be a large number of genetic sites, a mix of homozygous and heterozygous and then inter uterine and post birth developmental factors as well.
So what may be beneficial to an individual in reproductive success as a heterozygous genes in levels of arousal may lead to panic attacks and obsession in those with homozygous genes. But given that there are multiple expressions of depression and currently a growing number of indicated neurotransmitters and biological pathways: this statement is a gross over simplification.
And that is not even considering the developmental aspects differences in enzyme gradients that guide neural development of structure of the brain systems and there influence on later potential for dysfunction.