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Chromosome Crossing over

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Chromosome Crossing Over Do you ever wonder why two people besides identical twins are not alike? Our genes determine most of our physical characteristics, the exact combination of genes we inherit, and thus our physical traits is in part due to the process our chromosomes undergo, known as genetic recombination. Biology online states, that during meiosis, when homologous chromosomes are paired together, there are points along the chromosomes that make contact with the other pair. This point of contact is chiasmata, and can allow the exchange of genetic information between chromosomes. This further increases genetic variation. Recombination can occur between any two genes on a chromosome. The amount of crossing over is a function of how close the genes are to each other on the chromosome. If two genes are far apart, at opposite ends of the chromosome, more crossing over is possible. If the genes are closer together fewer crossing over is possible (McClean, 1998).
Two types of gametes are possible when following genes on the same chromosomes. If crossing over does not occur, the products are parental gametes. If crossing over occurs, the products are recombinant gametes. The allelic composition of parental and recombinant gametes depends upon whether the original cross involved genes in coupling or repulsion phase. It is easy to determine which gametes are recombinant because they are found in the lowest frequency (McClean, 1998).
In the 1930’s Harriet Creighton and Barbara McClintock studied two linked genes on chromosome 9 of a maize plant. One of the homologs contained two unique cytological markers. The markers consisted of densely stained knob at one end of the chromosome and a trans located piece of another chromosome 8 at the other end. The arrangements of these alleles and markers could be detected cytologically. Their work clearly established that crossing over had a cytological basis (Klug, Cummings, Spenncer, Palladino, 2012). In their experiment they used chromosome 9 markers, the colorless seed ( c ) and the waxy endosperm ( wx ). They created a heterozygote using the following characteristics, repulsion configuration of genetic markers and cytological landmarks on both ends of one chromosome. They found that the recombinant phenotypes each contained one of the cytological landmarks ( McClean, 1998).
We now know that most chromosomes contain a very large number of genes. Those that are part of the same chromosome are said to be linked and to demonstrate linkage in genetic crosses. Crossing over is the physical braking and rejoining process that occurs during meiosis. This process provides an enormous potential for genetic variation in gametes formed by any individual. The frequency of crossing over between any two loci on a single chromosome is proportional to the distance between them. Thus the percentage of recombinant gametes varies.
Harriet Creighton and Barbara McClintock studied crossing over on maize plants. They determined that crossing over had a cytological basis. Understanding how crossing over happens, explains why two people that are not identical twins are never alike. Genetic Variations are different for everyone.

References
Klug, W. S., Cummings, M. R., Spencer, C. A., Palladino, M. A. (2012). Concepts of Genetics. San Francisco, CA: Pearson Education Inc.
McClean, P. (1998). Recombination and Estimating the Distance Between Genes. Genetic Linkage. Retrieved from www.ndsu.edu/pubweb/~mcclean/plsc431/linkage/linkage2.htm
Independent Assortment and Crossing Over. Biology Online. Retrieved from http://www.biology-online.org/2/2_meiosis.htm

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