[QUOTE=grayarabpony;7202588]
Surely, Stoney, you do not mean that Mendelian inheritance never applies? As I said, for genes that are not on the same chromosome or closely linked, MI usually does apply.[/QUOTE]
No of course not, and aside from semantics I think that we closely agree with our attitudes towards line breeding in general. ETA: I think we are focusing on apples and oranges, because in re-reading Dawn was talking about specific diseases above, which may likely be inherited according to Mendelian models I havn’t looked at them specifically, whereas I am talking about how line breeding works as a whole in regards mainly to traits.
To clarify (hopefully) what I meant earlier:
If we want to talk about highly-penetrant genetic disease or a trait like eye color, then yes, it is likely that you can approximate with a Mendelian model and be highly accurate. However, the purpose of line breeding is not necessarily to breed for disease or lack of disease, but rather to amplify phenotypic traits in your breeding population. Most of these traits are not concretely defined by a single gene and therefore the pattern of inheritance may diverge from the Mendelian Ideal. I have done enough linkage analysis in my own research (as a post-doc at a well regarded University) to feel confident in saying that when looking at traits we will often find ourselves in the realm of partial penetrance and incomplete inheritance.
You cannot simply breed for a trait like a great neck according to the Mendelian model since we are talking about a trait made up of the influence of several genes which are linked either strongly or weakly, have varying levels of penetrance, and may or may not be inherited together. Line breeding is used to increase the homozygosity of the population, and through this to strengthen the linkage of the genes associated with “great neck” or some other trait (through increasing the chance that these genes will all be inherited together). Once this has been done, the penetrance will dictate the effect you will see once you breed outside blood into the population. The goal of outcrossing is to maintain the beneficial linkages establishing your desired trait while diminishing the liklihood of adverse linkages from being established in the population.
Then you have the general rinse and repeat over the generations that works to link traits together as well. This is the idea behind why Holstein has founded their breed on a specific few superior lines. They breed according to the lines, then bring in blood for a generation and then go strait back to their line breeding for subsequent generations in order to hopefully establish a linkage that embeds the traits they want in their breeding population. This is how they have linked traits together to establish the general “type” that they are so proud of.
For those that like links showing evidence (these are a select few, and may not be available outside of University. If anyone wants to read them, I will be happy to provide them directly, although I have to say they are highly science-oriented and all related to human health):
Outlines the application of Mendelian genetics versus non-Mendelian genetics (shows that GAP is correct about genes with high penetrance, but that it does not often apply):
http://www.nature.com/ng/journal/v33/n3s/pdf/ng1090.pdf
Outlines the fact that Mendelian inheritance patterns are important as “textbook examples” but “In most clinical genetics settings cases are seen where the disease diagnosed is well known to have a strong genetic component, and show some familial recurrence, but no clear Mendelian inheritance.” (Quote is from the text)
http://hmg.oxfordjournals.org/content/13/suppl_2/R225.full.pdf+html
Outlines that we have known that traits are not inherited according to a Mendelian model of genetics since the 1970s with examples on assessing traits and heritability (the example used is handedness in humans).
http://onlinelibrary.wiley.com/doi/10.1111/j.1749-6632.1977.tb41916.x/pdf