What is the difference between parental and recombinant chromosomes




















These are the gametes that are found in the lowest frequency. This is the direct result of the reduced recombination that occurs between two genes that are located close to each other on the same chromosome.

Also by looking at the gametes that are most abundant you will be able to determine if the original cross was a coupling or repulsion phase cross. For a coupling phase cross, the most prevalent gametes will be those with two dominant alleles or those with two recessive alleles.

For repulsion phase crosses, gametes containing one dominant and one recessive allele will be most abundant. Understanding this fact will be important when you actually calculate a linkage distance estimate from your data. The important question is how many recombinant chromosomes will be produced. If the genes are far apart on the chromosome a cross over will occur every time that pairing occurs and an equal number of parental and recombinant chromosomes will be produced.

Test cross data will then generate a ratio. But as two genes are closer and closer on the chromosome, fewer cross over events will occur between them and thus fewer recombinant chromosomes will be derived. We then see a deviation from the expected ratio. How can we decide how close two genes are on a chromosome? Because fewer crossover events are seen between two genes physically close togehter on a chromosome, the lower the percentage of recombinant phenotypes will be seen in the testcross data.

By definition, one map unit m. In honor of the work performed by Morgan, one m. Now let's determine the linkage distance between the genes pr and vg. What are Parental Type Chromosomes 3. What are Recombinant Type Chromosomes 4. DNA or genetic material can be exchanged when chiasmata are formed between non-sister chromatids of homologous chromosomes.

This occurs during the meiosis and it is the process called crossover. However, crossing over between homologous chromosomes is not a frequently occurring process. When crossover does not occur, homologous chromosomes separate into gametes without exchanging their genetic materials. Therefore, daughter cells get chromosomes that are similar to parental chromosomes. The allelic combinations remain same as they were in the parental chromosomes. Hence, there is no difference between the gene combinations of the parental and daughter cell chromosomes.

Resulting offspring phenotypes resemble the parents. Chromosomal crossover is the process that exchanges genetic material between homologous chromosomes. This occurs mainly during the meiotic cell division. When homologous chromosomes exchanged their genetic material, the resulting chromosomes bear new gene combinations.

Hence, they are known as recombinant chromosomes. Recombinant chromosomes are responsible for genetic variations between offsprings. Crossover is a normal process and it is an important process in sexual reproduction. Hence, the formation of recombinant chromosomes is not considered as a mutation. It does not result in a big change in genetic information due to the exchange of allelic positions between matching chromosomes unlike translocation a type of mutation which occurs between non-homologous chromosomes because crossover usually occurs when matching region of one homologous chromosome breaks and reconnect with the other matching region of the homologous chromosome.

Recombinant chromosomes result in offspring phenotypes that do not resemble parental phenotypes. They cause genetic diversity among the organisms. Crossing over between homologous chromosomes gives the chance of exchanging genetic materials between homologous chromosomes. What is meant by the quantitative term "recombination frequency"?

Before we start considering the occurrence and genetic outcomes of crossing-over, let's look again at something we already know, "Simple Mendelian Assortment for Two Genes on Different Chromosomes". In the standard Mendelian dihybrid cross involving two genes " alpha " and " beta " that undergo independent assortment i. Half of these gametes AB and ab are the same genotype as those produced by the original homozygous parental P organisms, and the other half Ab and aB are different.

If, however, the two genes alpha and beta are on the same chromosome, we would expect to get only two types of gametes, AB and ab , produced by the F1s. Figure 5. Now we are ready to start considering the genetic effects of crossing-over.



0コメント

  • 1000 / 1000