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I've been doing some research on breeding rabbits and saw many people mentioning that if you inbreed rabbits (father-daughter/mother-son/sister-brother) that there is only a small chance of birth defects and a chance at an improved outcome if the stock is already good.

There is another party that says inbreeding leads to serious side effects including fused spine, skeletal problems and missing or extra limbs example this video.

What does the science say? I would be interested to find a range of answers if there is a difference between "first generation" of inbreeding and if it makes a difference if recurring inbreeding happens?

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You mean for rabbits or in general, e.g. also for humans? It might be quite dependent on the species, e.g. number of chromosomes and gens etc. Anyway, I'm pretty sure that it gets worth if you keep inbreeding, because the number of identical gens (which can have defects) is increasing. – Martin Scharrer Apr 14 '12 at 11:58
One of the big concerns with inbreeding is that recessive defects that are extremely rare in the population and therefore (being recessive) are almost never expressed, could quite easily end up on both your loci if both the paternal and the maternal DNA are from the same original strain. Being diploid mammals, I don't see that rabbits could be excepted from this rule. – David Hedlund Apr 14 '12 at 12:30

1 Answer

Every time you reproduce there is a small probability of a mutations. Most of mutations are dangerous. But often since the baby will have one strand of DNA from one parents and one from the other, the probability of the two strands have the same mutation is really low. So the children will appear with no defects (I am grossly simplifying, some times a single strand mutated is enough to have a deadly mutation).

Now suppose a person A has a mutation in one strand of the DNA. He has 4 kids, two males: M1, M2 and two females: F1, and F2.

And now suppose that two of them M1 and F1, carry the mutation. The mutation appears as a different base in one of the chromosome. Now they reproduce, and make 4 children: b1, b2, b3, b4. Statistically each of them will have the mutation on both strands with a probability of 1/4. On only one of the strands with a probability of 1/2, and no mutation at all with a probability of 1/4.

So if a person has a silent mutation, and his kids interbreed they will make the mutation appear in full force with a probability of 1/4.

This says nothing respect to what the effect of the mutation is. It could be positive, or it could be negative. From a human perspective it is not acceptable to have a probability of 1/4 for a children to have a mutation (not to mention the 1/2 to carry it in a silent way). But from Nature point of view this only rises the probability of having mutations. Something which Nature can still cope quite well (still because there is a mutation threshold after which the number of viable offspring is too low for the species to reproduce). After all the mutations that lead to birth defects has often limited effect (species-wise), while a mutation that causes a neutral or a positive mutation can have a positive impact on the species. So you would not interbreed human beings. But in the past it has been considered acceptable to interbreed some animals looking to extend specific traits.

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'severe birth defects' is an overloaded term, but humanity has a long history of fairly harmful genetic traits that are carried around as recessive genes. This is where, for instance, the strong association between inbreeding and Hemophelia comes from, and a similar effect is seen in tightly-knit ethnic communities, such as Tay-Sachs disease among Ashekenazi Jews. – LessPop_MoreFizz Apr 14 '12 at 15:07
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Welcome to Skeptics! Please provide some references to support your claims - in particular that this simplified view of genetics is accurate enough to predict the effects you claim. – Sklivvz Apr 15 '12 at 12:46

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