The answer is <span>a. Each gene is at the same locus on both chromosomes.
Since e</span><span>ach gene is at the same locus on both chromosomes, they are able to pair correctly before they separate in meiosis. They never produce identical phenotypes. Also, the genes and alleles on the homologous chromosomes are not identical. </span>
Answer:
Each mutant would be mated to wild type and to every other mutant to create diploid strains. The diploids would be assayed for growth at permissive and restrictive temperature. Diploids formed by mating a mutant to a wild type that can grow at restrictive temperatures identify the mutation as recessive. Only recessive mutations can be studied using complementation analysis. Diploids formed by mating two recessive mutants identify mutations in the same gene if the diploid cannot grow at restrictive temperature (non-complementation), and they identify mutations in different genes if the diploids can grow at restrictive temperature (complementation).
Explanation:
Recessive mutations are those whose phenotypic effects are only visible in homo-zygous individuals. Moreover, a complementation test is a genetic technique used to determine if two different mutations associated with a phenotype colocalize in the same <em>locus</em> (i.e., they are alleles of the same gene) or affect two different <em>loci</em>. In diploid (2n) organisms, this test is performed by crossing two homo-zygous recessive mutants and then observing whether offspring have the wild-type phenotype. When two different recessive mutations localize in different <em>loci</em>, they can be considered as 'complementary' since the heterozygote condition may rescue the function lost in homo-zygous recessive mutants. In consequence, when two recessive mutations are combined in the same genetic background (i.e., in the same individual) and they produce the same phenotype, it is possible to determine that both mutations are alleles of the same gene/<em>locus</em>.
So basically you will have to label the purple parent 1 and whatever gene that is then the same for parent 2 here is an example of a punnet square so maybe you can understand better
The supporting structure of the cell that is also involved in movement is most likely the cytoskeleton.
Answer:
Any population in a given environment contains a variety of available, inheritable genetic traits. ... In a population, there is a cause-and-effect relationship between the variation of traits and the probability that specific organisms will be able to survive and reproduce.
Explanation: