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IB DP Biology Study Notes

4.8.6 Meiosis and Genetic Diversity

Unlock the complexities of meiosis and its vital role in generating genetic diversity. Delve into segregation, independent assortment, the usefulness of Punnett grids in genetic predictions, and demystify the exceptions to Mendel’s famed second law.

Segregation and Independent Assortment in Meiosis

Meiosis: A Detailed Overview

  • Meiosis is a two-stage process of cell division, consisting of Meiosis I and Meiosis II.
    • In Meiosis I, one diploid parent cell divides into two non-identical haploid daughter cells.
    • In Meiosis II, these two haploid cells divide once again, resulting in four non-identical haploid daughter cells.
  • Meiosis is fundamental for sexual reproduction as it ensures variation in offspring.
Meiosis I and Meiosis II overview.

Image courtesy of Rdbickel

Law of Segregation

  • Stemming from Gregor Mendel's First Law, the Law of Segregation emphasises that:
    • Individuals have two alleles for each trait.
    • During gamete formation, these alleles segregate so that each gamete carries only one allele for each trait.
    • When gametes fuse during fertilisation, the resulting offspring has two alleles for the trait, one from each parent.
A diagram of Mendel's First Law, the Law of Segregation.

Image courtesy of CNX OpenStax

Law of Independent Assortment

  • Mendel's Second Law states:
    • Alleles for separate traits are passed independently of one another.
    • During Meiosis I, how one pair of homologous chromosomes aligns and segregates is independent of how any other pair does so.
    • However, genes located on the same chromosome can affect this independence.
A diagram of Mendel's second Law, the Law of independent assortment.

Image courtesy of LadyofHats

Using Punnett Grids for Dihybrid Crosses

The Essence of Dihybrid Crosses

  • Dihybrid cross is a breeding experiment that tracks the inheritance of two traits simultaneously.
  • It's foundational for understanding how traits are passed on across generations.

How to Construct Punnett Grids for Dihybrid Crosses

  • Punnett grids serve as predictive tools for genetic combinations.
    • Begin with a 4x4 grid.
    • For each parent, determine the possible allele combinations for their gametes.
    • List all possible gamete combinations for one parent on the top and for the other on the left.
    • By pairing these combinations, fill out the squares in the grid. This gives all possible genotypes for the offspring.
    • Based on this, it's easier to deduce the phenotypic and genotypic ratios for the offspring.

Exceptions to Mendel’s Second Law

Linked Genes: A Challenge to Mendel’s Second Law

  • Genes on the same chromosome are often "linked" and tend to be inherited together.
  • This is because they do not sort independently, presenting an exception to Mendel's second law.
  • Gene linkage reduces the variety of combinations that can result from meiosis.

The Magic of Crossing Over

  • Nature has a way of introducing variety, even with linked genes.
  • During Prophase I of Meiosis I, homologous chromosomes can exchange segments, a process known as crossing over.
    • This can separate genes that were previously linked.
    • The result is genetic recombination where new allele combinations form.
    • The closer two genes are on a chromosome, the less likely they will be separated by crossing over.
Linked genes, unlinked genes and crossing over

Image courtesy of SrKellyOP

Incomplete Dominance, Codominance, and Beyond

  • Not all genetic traits strictly adhere to Mendel's laws. Some patterns include:
    • Incomplete dominance: Here, the heterozygote has a phenotype that's intermediate between the two homozygotes. For instance, a red-flowered plant crossed with a white-flowered plant might produce pink flowers.
    • Codominance: Both alleles express themselves fully in a heterozygote. An example is blood type AB where both A and B alleles are expressed.

The Intricacies of Multiple Alleles and Polygenic Inheritance

  • Some genes have more than just two allele forms, termed multiple alleles. A prime example is the human blood group system with A, B, and O alleles.
  • Polygenic inheritance is when several genes, often located on different chromosomes, influence a single trait. This creates a range of phenotypes, like human skin colour or height, which don't fit simple Mendelian patterns.

FAQ

Genetic diversity is the total number of different genes present in a population. This diversity is essential as it allows populations to adapt to changing environments. With a broader gene pool, there's a higher chance that some individuals will possess genetic combinations allowing them to survive under new conditions. Those individuals can then reproduce and pass on their advantageous genes. Without genetic diversity, populations are more susceptible to diseases, environmental changes, and other threats, as they may lack the necessary genetic resources to adapt. Over time, reduced genetic diversity can increase the risk of extinction for a species.

Errors during meiosis can lead to disorders stemming from an abnormal number of chromosomes in gametes, a condition called aneuploidy. One of the most well-known consequences of such an error is Down's syndrome, which results from an extra copy of chromosome 21. Errors can arise during Anaphase I if homologous chromosomes fail to separate properly, termed non-disjunction. Similarly, non-disjunction can occur in Anaphase II if sister chromatids don't separate. The resulting gametes will either have an extra chromosome or lack one. When these gametes are involved in fertilisation, the resulting zygote will have an abnormal chromosomal number, potentially leading to developmental abnormalities or miscarriages.

Scientists determine if genes are linked by observing the inheritance patterns over several generations. If two genes are located close together on the same chromosome, they are more likely to be inherited together and are considered linked. When performing a dihybrid cross involving potentially linked genes, the expected ratio for independent assortment (based on Mendel's Second Law) is 9:3:3:1. However, if the observed ratios deviate significantly from this, it suggests that the genes may be linked. Further evidence can be gathered through test crosses and by calculating the recombination frequency: a low recombination frequency indicates that genes are closely linked.

A monohybrid cross and a dihybrid cross are techniques used in genetics to study the inheritance of specific traits. A monohybrid cross involves the study of a single trait and its two possible alleles. The Punnett square for a monohybrid cross is typically 2x2, representing the two possible gamete combinations from each parent. On the other hand, a dihybrid cross examines the inheritance of two distinct traits simultaneously, each having two possible alleles. This results in a more complex 4x4 Punnett grid. While monohybrid crosses showcase the basic principles of inheritance, dihybrid crosses give insight into how different traits can be inherited together.

Meiosis and mitosis are both cell division processes, but they serve distinct purposes and result in different outcomes. Mitosis results in two genetically identical diploid daughter cells and is primarily for growth, repair, and general maintenance of the organism. In contrast, meiosis leads to the production of four non-identical haploid gametes. The key stages in meiosis, such as crossing over during Prophase I and the random assortment of chromosomes, introduce significant genetic variation. This variation ensures that offspring inherit a unique combination of alleles from their parents, a cornerstone of evolution and adaptability in sexually reproducing populations.

Practice Questions

Explain the differences between Mendel’s First and Second Law using the context of meiosis. How do these laws relate to the genetic diversity observed in sexually reproducing organisms?

Mendel's First Law, also known as the Law of Segregation, states that every individual possesses two alleles for any particular trait, and each parent passes on a randomly selected allele to its offspring. This is observed during meiosis when homologous chromosomes separate, ensuring each gamete receives only one allele for a trait. Mendel's Second Law, the Law of Independent Assortment, posits that genes for different traits assort independently of one another during gamete formation. This is evident during Meiosis I, where homologous chromosomes align randomly at the metaphase plate, leading to the independent assortment of genes. Both laws, combined with the genetic mixing during fertilisation, play pivotal roles in generating genetic diversity in sexually reproducing organisms.

Describe the significance of crossing over in relation to Mendel’s Second Law. How does this process contribute to genetic diversity?

Crossing over is a vital process occurring during Prophase I of Meiosis I, where homologous chromosomes exchange genetic material. This phenomenon can separate genes that are close together on the same chromosome, introducing new allele combinations. While Mendel's Second Law claims that genes sort independently, this isn't strictly true for genes on the same chromosome; they're usually linked and inherit together. Crossing over acts as an exception to this linkage, introducing genetic recombination and breaking the expected patterns of inheritance. This genetic reshuffling ensures a higher degree of genetic diversity in the offspring, enhancing the variation within a population.

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