In: Biology
A Drosophila female homozygous mutant for two recessive
genes (a
and b) is crossed to a wild-type male. The F1 are all
wild-type. An F1 female is crossed to a double-mutant male and the
following phenotypes were seen in the F2:
| 
 a b  | 
 497  | 
| 
 + +  | 
 460  | 
| 
 a +  | 
 465  | 
| 
 + b  | 
 426  | 
| 
 Total  | 
 1848  | 
Perform a “best fit” or apriori
χ2 analysis to determine if genes
a
and b assort independently. Give the value for
χ2, DF and Probability; as well as your decision. Are
these genes linked? Use the method you used in Statistics lab and
round to two decimal places throughout.
| 
 χ2 = 5.48, DF = 3, prob < 0.05, reject, linked  | 
||
| 
 χ2 = 8.45, DF = 3, 0.1 < prob < 0.9. accept, not linked  | 
||
| 
 χ2 = 4.58, DF = 4, 0.1< prob< 0.5, accept, not linked  | 
||
| 
 χ2 = 5.48, DF = 3, 0.1 < prob < 0.5, accept, not linked  | 
Given that the female is homozygous mutant for the two recessive genes a and b. Means, its genotype is, aa bb. The genotype of a pure breed Wild-type male is, AA BB. Cross between these two will have the progeny with the following genotypes.
aa bb* AA BB -----> Aa Bb (All wild-type) -------> F1
Cross between F1 female and double-mutant male (aa bb) will have the progeny with the following genotypes.
Aa Bb* aa bb ----> Aa Bb (++) (1/4, all wild-type), Aa bb (+b) (1/4, mutant for b), aa Bb (a+) (1/4, mutant for a), aa bb (ab) (1/4, double mutant)
The given phenotypes are in approximately equal ratios similar to that of the expected phenotypes.
CHI - SQUARE (X2):
X2 = Σ(O - E)2 / E
Where O = Observed frequency
E = Expected frequency
| 
 Phenotype  | 
 O  | 
 E  | 
 (O-E)  | 
 (O-E)^2  | 
 (O-E)^2/E  | 
| 
 A_B_  | 
 497  | 
 462  | 
 35  | 
 1225  | 
 2.651515  | 
| 
 A_bb  | 
 460  | 
 462  | 
 -2  | 
 4  | 
 0.008658  | 
| 
 aa A_  | 
 465  | 
 462  | 
 1.5  | 
 2.25  | 
 0.155172  | 
| 
 aa bb  | 
 426  | 
 462  | 
 -36  | 
 1296  | 
 2.805195  | 
| 
 2.815345  | 
The degrees of freedom (DF) = n-1 = 4-1 = 3
The calculated P value is p < 0.421856, which is not significant at p< 0.05. So, we accept the null hypothesis.
The difference between the expected an observed phenotypic ratios is not significant and the genes are assorting independently.