von John Armstrong
Wie würden Sie die Auswirkungen eines berühmten Champions auf seine Rasse bestimmen?
Ein Hund, der viele Shows und viele Titel gewonnen hat, war als Gestüt recht beliebt und hat möglicherweise mehr Nachkommen gezeugt als andere männliche Nachkommen. Dies garantiert jedoch nicht, dass er in fünf oder zehn Generationen mehr Einfluss hat als ein anderer Hund, der nur zwei- oder dreimal gezüchtet wurde.
Wenn ausreichende Daten verfügbar sind, können Sie die prozentuale Bedeutung eines Vorfahren ermitteln, indem Sie seinen prozentualen Beitrag zu den aktuellen Hunden berechnen. Der prozentuale Anteil (auch als
Prozentsatz von Blut
bezeichnet) wird durch die Weitergabe der Gene von den Eltern an die Nachkommen bestimmt. Eine Individuell erbt einen Satz von Chromosomen und die Gene, die sie tragen, von ihrem Vater und einen zweiten, homologen
(gleichwertigen) Satz von der Mutter. Somit leistet jedes Elternteil einen Beitrag von 50%. Da die Eltern in jeder Generation immer 50% ihrer Gene zu ihren Nachkommen beitragen, scheint es vernünftig zu erwarten,
dass 25% von jedem Großelternteil kommen, 12,5% von jedem Urgroßelternteil und so weiter.
Sobald wir jedoch an den Eltern vorbei sind, handelt es sich um Wahrscheinlichkeiten, nicht um Gewissheiten. Das ist kein Mischen von Farbe! Wenn Papa Ihnen einen Satz seiner Chromosomen passiert, werden sie eine Auswahl von den beiden Elternteilen enthalten, aber es gibt keine Garantie dafür, dass die Auswahl genau gleich ist. Es gibt sogar eine kleine Chance (sehr klein), dass er die von nur einem seiner Eltern weitergibt. Wenn wir 10 Generationen zurückerhalten, würde der Beitrag jedes der 1024 Vorfahren theoretisch etwas weniger als 0,1% betragen. Doch in der Stammbaum des durchschnittlichen Rassehund, gibt es selten mehr als 100 bis 200 verschiedene Namen und einige erscheinen 50mal oder mehr. Dies sind die wesentlichen Vorfahren, die die große genetische machen Wenn Sie einen Stammbaum haben, können Sie den prozentualen Beitrag von Wiederholungen berechnen, indem Sie einfach die Häufigkeit, mit der jeder Vorfahr in einer Generation auftaucht, mit dem entsprechenden Prozentsatz für multiplizieren diese Generation und addieren dann alle berechneten Prozentsätze der Beiträge jeder Generation. Die unten aufgeführte Tabelle zeigt den Prozentsatz an Blut, der von jedem Vorfahren in den angegebenen Generationsstufen geerbt wurde. Generation "1" ist die Eltern.
|Genetischer Beitrag der Vorfahren|
You should get a number between 0 and 1; multiply by 100% to get the % contribution. Databases exist for many breeds that will contain the data enabling you to extend a pedigree to 10 generations or more. Manual computation, though tedious, is still possible, but hardly convenient. Several pedigree programs will quickly calculate % contribution for selected ancestors or all ancestors for a specified number of generations, providing you with information on which dogs have been most influential.
While most breeders recognize that a mating between half-sibs or cousins represents inbreeding, the majority probably have no idea which is the closer relationship. This is not helped by the non-standard definition of inbreeding in some books (e.g. Onstott's "Breeding Better Dogs").
The standard definition of inbreeding is that it is any scheme which results in the sire and the dam having common ancestors. Many breeders use the term "inbreeding" for close relatives and "linebreeding" for more distantly related individuals, but there is no fundamental difference. The parameter used to express this common heritage is called the inbreeding coefficient and was first proposed by Sewell Wright in 1922. Designated F by Wright (but more commonly IC or COI by breeders), it can theoretically range from 0 to 100%, and indicates the probability that the two alleles for any gene are identical by descent .
The primary consequence of inbreeding is to increase homozygosity. However, the IC is not a direct measure of homozygosity because the two alleles passed down from different ancestors may be functionally the same. Furthermore, some proportion of all the genes will be the homozygous because there is only one allele. The IC serves as an indicator of what proportion of the remainder may have been made homozygous by inbreeding.
The inbreeding coefficient is a function of the number and location of the common ancestors in a pedigree. It is not a function, except indirectly, of the inbreeding of the parents. Thus, one can mate two highly inbred individuals who share little common ancestry and produce a litter with a very low IC. (Because the potential number of ancestors doubles every generation, eventually you reach a point where the number of ancestors exceeds the number of individuals alive at that time. You are, therefore, bound to find some common ancestors if you go back far enough.). Conversely, it is possible to mate two closely related dogs, both of which have low ICs, and boost the IC substantially.
The most widely used approach for calculating inbreeding coefficients is Wright's "paths" method ( see note ) , best illustrated by a simple example. Suppose we mate half-sibs, the common ancestor, Anson, being the father. Don is the son of Anson and Bess; Eva the daughter of Anson and Claire. Fred is one of their progeny.
To simplify, we don't show the ancestors that aren't shared:
Now we consider a gene for which Anson carries two different alleles, a1 and a2 . There is a 50% probability of the allele Anson passed to Don being passed on to Fred. There is also a 50% probability that the same allele will be passed from Anson to Eva, and a 50% probability of it being passed from Eva to Fred, if Eva got it. When dealing with events that are contingent (this * and * that must happen), we multiply the probabilities - in this case 0.5 x 0.5 x 0.5 = 0.125 (12.5%). This final number is the probability that Fred will be homozygous for either a1 or a2 because of the common grandfather.
In general, Wright's method is to determine the path from Fred to the common ancestor, Anson, and back again on the other side of the pedigree (Fred-Don-Anson-Eva-Fred), count the number of individuals in the path, excluding Fred (there are 3, Don-Anson-Eva) and then calculate ½ n , where n is that number. So, in the present case, we have (½) 3 or (½ x ½ x ½) = 1/8, or 12.5%. If this were the only common ancestor, the inbreeding coefficient for Fred would be 12.5%.
Now, suppose the common ancestor was one of the grandfathers of the parents (i.e. a great-grandfather of the litter). This adds an individual on each side of the pedigree, so that we will get a path of the type Fred-X-Don-Anson-Eva-Y-Fred, and the inbreeding on Anson will be (1/2) 5 or 1/32 (3.125%).
Like many other genetic calculations, the IC is based on probabilities, not certainties. An individual may be more or less highly inbred than the number computed.
If we had only a single common ancestor to deal with, life would be relatively simple. However, there are two complications to deal with. The first is that there will be more than one common ancestor. Let's consider the case of first cousins. In human populations such a pairing is prohibited in some societies but allowed in others. We have already calculated the inbreeding for a single shared grandparent. First cousins have two shared grandparents, and we simply add the inbreeding coefficient for each to get 6.25%.
The second complication is that the common ancestor may be inbred. If so, his or her inbreeding coefficient will have to be calculated. To account for this we have to multiply the inbreeding coefficient calculated for Fred by (1 + F A ), where F A is the inbreeding coefficient calculated for Anson. For example, if Anson is the product of a mating of first cousins, the total inbreeding for Fred will be 0.125 x 1.0625 = 0.133 (13.3%) if there are no other shared ancestors in the pedigree.
Unfortunately, in the average pedigree, there are a large number of shared ancestors. Therefore, the total inbreeding for a dog cannot generally be calculated manually and appropriate software must be used. Calculating inbreeding for only the first few generations is not particularly useful. If there are more than one or two common ancestors in four or five generation pedigree, the inbreeding is probably already higher than desirable. Unfortunately, having none is no guarantee that common ancestors will not occur in abundance further back, and some pedigrees of this type still achieve moderately high inbreeding coefficients. Neither can be number of shared ancestors be used as a reliable guide, as the inbreeding coefficient is very sensitive to when and where they occur in a pedigree.
Suppose a breeder has two bitches (A and B) she wants to mate to different males. After careful research she has identified three potentially suitable males (C, D and E), all of which look equally good. She hopes to get a male puppy from one litter and a female from the other, and would like to eventually breed them to each other. The objective could be to pick the combination that will minimize the potential inbreeding. Alternatively, she may be looking for two dogs that are not close relatives yet have similar heritage.
One approach would be to produce hypothetical litters for all combinations: AC, AD, AE, BC, BD and BE. Then we would have to look at the possibilities for the second generation. There will be six if we don't permit shared grandparents, and 36 if there are no restrictions. These potential litters could then be evaluated for inbreeding or the % contribution of significant ancestors. This will certainly provide the data, but is unnecessarily tedious.
The coefficient of relationship (RC) provides a way of objectively assessing the similarity of two pedigrees by giving a number that is a direct measure of shared ancestry. In most human populations, two individuals picked at random would likely have a RC of 0, a brother and sister 50% and identical twins 100%. Other relationships would fall between 0 and 50%.
The number generated may be viewed as analogous to the % composition, except that you are comparing two dogs instead of looking at one. A brother and sister will give a value of 50% as long as an ancestor is not repeated. Once ancestors start to repeat, the individuals no longer have an inbreeding coefficient of zero. Two sibs from a highly inbred line may have an RC of 80% or more, and two dogs that are not sibs may have an RC above 50%.
The formula for the RC is:
R AB = 2 f AB ÷ [(1 + F A )(1 + F B )] ½
where f AB is the inbreeding coefficient of a hypothetical litter between A and B, and F A and F B are the inbreeding coefficients for the two individuals, A and B.
A simpler approach to the breeder's problem would be to compute the RCs for C vs D and E, and D vs E. This is not a pencil and paper calculation. However, presented with just such a problem, it took me
about 2 minutes to obtain the three RCs with the latest version of CompuPed. My results were:
As D and E share the most common ancestry, so would the progeny from their two prospective litters, while C and D share the least. To minimize inbreeding and maximize diversity, they would be my choice, all else being equal. (These values actually all fall below the average for the breed, which is ~ 23%.).
The f AB term in the RC equation is sometimes called the "kinship coefficient" and may also be used as a measure of the relationship between two individuals. It's computation is the same as that of an inbreeding coefficient for a hypothetical litter between the two dogs. (It doesn't matter if they are the same sex.)
The mean kinship ( mk i ) for individual i is is the average of the kinship coefficients ( f ij ) between i and all the other breedable individuals in the population:
A conservation biologist would consider the individual with the lowest mean kinship to be the most genetically valuable in terms of maintaining diversity in the population, and would try to favor that individual in a breeding program.
Note : An alternative approach, often referred to as the "tabular" method, calculates inbreeding from the ealiest ancestor forward to the current dog (or dogs).