Reciprocal cross

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In genetics, a reciprocal cross is a breeding experiment designed to test the role of parental sex on a given inheritance pattern. [1] All parent organisms must be true breeding to properly carry out such an experiment. In one cross, a male expressing the trait of interest will be crossed with a female not expressing the trait. In the other, a female expressing the trait of interest will be crossed with a male not expressing the trait. It is the cross that could be made either way or independent of the sex of the parents. For example, suppose a biologist wished to identify whether a hypothetical allele Z, a variant of some gene A, is on the male or female sex chromosome. They might first cross a Z-trait female with an A-trait male and observe the offspring. Next, they would cross an A-trait female with a Z-trait male and observe the offspring. Via principles of dominant and recessive alleles, they could then (perhaps after cross-breeding the offspring as well) make an inference as to which sex chromosome contains the gene Z, if either in fact did.

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Reciprocal cross in practice

Given that the trait of interest is either autosomal or sex-linked and follows by either complete dominance or incomplete dominance, a reciprocal cross following two generations will determine the mode of inheritance of the trait.

White-eye mutation in Drosophila melanogaster

Sex linkage was first reported by Doncaster and Raynor in 1906 [2] who studied the inheritance of a colour mutation in a moth, Abraxas grossulariata. Thomas Hunt Morgan later showed that a new white-eye mutation in Drosophila melanogaster was also sex-linked. He found that a white-eyed male crossed with a red-eyed female produced only red-eyed offspring. However, when they crossed a red-eyed male with a white-eyed female, the male offspring had white eyes while the female offspring had red eyes. The reason was that the white eye allele is sex-linked (more specifically, on the X chromosome) and recessive.

The analysis can be more easily shown with Punnett squares:

Table 1. Wild-type Male x Mutant Female ( X(wt)Y x X(mut)X(mut))
X (mut)X (mut)
X (wt)X (mut) X (wt)

Red eye Female

X (mut) X (wt)

Red eye Female

YX (mut) Y

White eye Male

X (mut) Y

White eye Male

Table 2. Mutant Male x Wild-type Female ( X(mut)Y x X(wt)X(wt) )
X (wt)X (wt)
X (mut)X (mut) X (wt)

Red eye Female

X (mut) X (wt)

Red eye Female

YX (wt) Y

Red eye Male

X (wt) Y

Red eye Male

As shown in Table 1, the male offspring are white-eyed and the female offspring are red-eyed. The female offspring are carrying the mutant white-eye allele X(mut), but do not express it phenotypically because it is recessive. Although the males carry only one mutant allele like the females, the X-chromosome takes precedence over the Y and the recessive phenotype is shown.

As shown in Table 2, all offspring are Red-eyed. The males are free of the mutation. The females however, are carriers. [3]

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The genotype of an organism is its complete set of genetic material. Genotype can also be used to refer to the alleles or variants an individual carries in a particular gene or genetic location. The number of alleles an individual can have in a specific gene depends on the number of copies of each chromosome found in that species, also referred to as ploidy. In diploid species like humans, two full sets of chromosomes are present, meaning each individual has two alleles for any given gene. If both alleles are the same, the genotype is referred to as homozygous. If the alleles are different, the genotype is referred to as heterozygous.

<span class="mw-page-title-main">Mendelian inheritance</span> Type of biological inheritance

Mendelian inheritance is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866, re-discovered in 1900 by Hugo de Vries and Carl Correns, and later popularized by William Bateson. These principles were initially controversial. When Mendel's theories were integrated with the Boveri–Sutton chromosome theory of inheritance by Thomas Hunt Morgan in 1915, they became the core of classical genetics. Ronald Fisher combined these ideas with the theory of natural selection in his 1930 book The Genetical Theory of Natural Selection, putting evolution onto a mathematical footing and forming the basis for population genetics within the modern evolutionary synthesis.

<span class="mw-page-title-main">Dominance (genetics)</span> One gene variant masking the effect of another in the other copy of the gene

In genetics, dominance is defined as the interactions between alleles at the same locus on homologous chromosomes and the associated phenotype. In the case of complete dominance, one allele in a heterozygote individual completely overrides or masks the phenotypic contribution of the other allele. The overriding allele is referred to as dominant and the masked one recessive. Complete dominance, also referred to as Mendelian inheritance, follow Mendel's laws of segregation. The first law states that each allele in a pair of genes is separated at random and have an equal probability of being transferred to the next generation, while the second law states that the distribution of allele variants is done independently of each other. However, this is not always the case as not all genes segregate independently and violations of this law are often referred to as "non-Mendelian inheritance".

Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction. Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart. In other words, the nearer two genes are on a chromosome, the lower the chance of recombination between them, and the more likely they are to be inherited together. Markers on different chromosomes are perfectly unlinked, although the penetrance of potentially deleterious alleles may be influenced by the presence of other alleles, and these other alleles may be located on other chromosomes than that on which a particular potentially deleterious allele is located.

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<span class="mw-page-title-main">Hereditary carrier</span> Organism with a recessive genetic allele that does not display the recessive trait

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References

  1. reciprocal cross definition
  2. Doncaster L and Raynor GH (1906). Breeding experiments with Lepidoptera. Proceedings of the Zoological Society of London, 1:125–133.
  3. Fruit Fly Genetics