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  Section: Genetics » Linkage and Crossing Over in Diploid Organisms (Higher Eukaryotes)
 
 
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Recombination frequencies from a test-cross

 
     
 
Content
Linkage and Crossing Over in Diploid Organisms (Higher Eukaryotes)
Coupling and repulsion hypothesis
A testcross in maize
Crossing over and meiosis 
Crossing over and chiasma formation
Mechanism of genetic recombination
Crossing over and linkage maps 
Recombination frequencies from a test-cross
Recombination frequencies from F2 data
Interference and coincidence
Linkage maps
Mapping function and poisson distribution
Linkage groups
Chi-square test 
Cytological basis of crossing over
Creighton and McClintock's experiment in corn
Meselson and Weigle's experiment using lambda (λ) phage
Crossing over at four strand stage


Crossing Over and Linkage Maps
Recombination frequencies from a test-cross
(A three-point testcross)
Since recombination frequencies are directly proportional to distances between genes in question, these values can be used in preparation of linkage maps. A three-point testcross (involving three genes) to be discussed in this section not only gives us information regarding relative distances between these genes, but also tells us the linear order in which these genes should be present on the chromosome. The underlying basic principle involved in preparation of linkage maps can be explained by using a hypothetical example.

Let us presume that there are three genes A, B and C present on the same chromdsome (i.e. these are linked). There could be three possible linear orders in which these genes may be present on a chromosome. These are A-B-C, A-C-B or B-A-C. As is obvious, that in one case B is present in the middle, while in the other two cases C and A respectively are present at the middle position. Therefore, in finding out the linear order, one has to really find out the gene which is present in the centre. For this purpose a three point test-cross is made, which involves crossing of a trihybrid ABC/abc (obtained from a cross ABC/ABC x abc/abc) with triple homozygous recessive abc/abc. The progeny obtained will represent the gametes formed by the hybrid. Presuming A-B-C as the order of genes, results expected can be diagrammatically represented as in Figure 10.8.
 
A three-point testcross involving three hypothetical genes A, B and C.
Fig. 10.8. A three-point testcross involving three hypothetical genes A, B and C.

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Hypothetical frequencies of eight types of progenies are listed in Table 10.2. The following procedure will be followed for the preparation of If crossing over, i.e. recombination value (per cent) between A and B is called X, that between B and C is called Y and that between A land C is called Z, then



From the above values of X, Y and Z, order of genes can be worked out and the linkage map can be prepared using the following criteria : if Z = X + Y, order of genes is A-B-C; if Z = X - Y, order of genes is A-C-B, if Z = Y - X, order of genes is B-A-C.

Preparation of a linkage map can be further illustrated by using an example from maize involving three endosperm characters. These three characters are coloured aleurone (C) versus colourless aleurone (c), full endosperm (Sh) versus shrunken endosperm (sh) and non-waxy endosperm (Wx) versus waxy endosperm (ws). The data reported by C.B. Hutchinson in 1922 in a three-point testcross are presented in Figure 10.9. As shown in previous hypothetical example, three recombination values i.e. C-Sh, Sh-Wx and C-Wx would be worked out in order to find out the linear order of the three genes C, Sh and Wx.
 
A three-point testcross in maize involving three genes, coloured (C) vs colourless (c), full (Sh) vs shrunken (sh) and non-waxy (Wx) vs waxy (wx).
Fig. 10.9. A three-point testcross in maize involving three genes, coloured (C) vs colourless (c), full (Sh) vs shrunken (sh) and non-waxy (Wx) vs waxy (wx).

In data presented in Figure 10.9, C and sh are present together in P1 Therefore, the progeny showing their separation would be recorded as recombination between C and Sh.



In this case, recombination value C-Wx (21.7%) is close to (C-sh) + (sh-Wx) = 3.5 + 18.4 = 21.9%. Therefore, sh should be located between C and Wx. The slight difference between the total of two individual values and the third value is due to the fact that in the third value (C-Wx), double-cross-overs are not included. However, if (C-Wx) were close to (C-sh) - (sh-Wx), then Wx would be between C and sh. The linkage map based on the data given in Figure 10.9 is given in Figure 10.10, where 1 map unit (m.u.) is considered equal to 1% recombination. A map unit is sometimes referred to as centiMorgan (cM) in honour of Thomas Hunt Morgan (for long distances on a map the linear relationship between cM units and recombination frequency does not hold good; see later for details).

To the linkage map shown in Figure 10.10, other genes may be added by performing other three-point testcrosses where two genes already placed on linkage map may be included.
 
A linkage map prepared from results presented in Figure 10.9.
Fig. 10.10. A linkage map prepared from results presented in Figure 10.9.

 
     
 
 
     




     
 
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