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15.2 Genes, inheritance and meiosis

Elizabeth Dahlhoff and Melissa Hardy

Learning Objectives

By the end of this section, you will be able to do the following:

  • Understand the central importance of DNA as information molecule for genetics.
  • Be able to differentiate between genotype and phenotype.
  • Recognize the relationship between alleles, allelic variation, and homologous chromosomes.
  • Review role of meiosis in genetic information flow.

Molecular basis of genetics and evolution

Genetics is the study of how traits are inherited. A trait is defined as a variation in the physical appearance of a heritable characteristic. It seeks to understand how traits are passed from generation to generation. Before you start learning about the details of inheritance, let’s review some topics that are important in order to understand genetics.  Recall that genes are segments of DNA that are typically several hundred or thousand bases long. Each gene directs the production of a protein through the process of protein synthesis: DNA gets transcribed to produce an mRNA; mRNA provides to code for a ribosome to produce a chain of amino acids.
Organisms get their traits from the proteins expressed in their bodies; proteins are produced using the information found in the organism’s DNA. Variation in the DNA between different organisms causes the production of proteins that contain differing orders of amino acids. These proteins can have different shapes and therefore different functions. When proteins function differently, this leads to differences in traits. In fact, you could say that proteins are ultimately the material upon which natural selection operates, while DNA is the blueprint of that action over time.
Consult Making and using the molecules of life if you need to review this topic.
Amoeba sisters- deconstructed DNA
Figure 1. Left Panel: The central dogma of biological information flow. Right Panel: Eukaryotic DNA is found on chromosomes. (Image credits: Wikimedia Commons)
Recall that eukaryotic genes are found on chromosomes and that each eukaryotic chromosome typically contains hundreds or thousands of genes. In most eukaryotes, including humans and other animals, each cell contains two copies of each chromosome. The reason we have two copies of each gene is that we inherit one from each parent. In contrast to eukaryotes, prokaryotes (and mitochondria and chloroplasts) have a circular chromosome. This means they have as many copies of each gene as they have chromosomes; in bacteria, that is usually one, but organelles like mitochondria and chloroplasts have more than one copy their circular chromosome per cell. Nuclear chromosomes are inherited by the offspring from the parents via the egg or sperm. Inside one egg or one sperm is one copy of each chronometer (so 23 total in humans). When an egg is fertilized by a sperm, the resulting zygote (fertilized egg) will contain two copies of each chromosome, just like each of its parents. In contrast, organelle DNA is only inherited from the maternal parent.

Figure 2: Nuclear versus organelle (maternal) inheritance (Image credit: Understanding Science Website, UC Berkeley).

Meiosis

Meiosis is the process that produces eggs and sperm. Eggs and sperm are also known as gametes. During meiosis, one copy of each paired chromosome is moved into the gamete. Cells with one copy of each chromosome are known as “haploid“. This separation, or segregation, of the homologous (paired) chromosomes means also that only one of the copies of the gene gets moved into a gamete. The offspring are formed when that gamete unites with one from another parent and the two copies of each gene (and chromosome) are restored.

The offspring will receive two copies of each nuclear gene (one from each parent), but the copies are not necessarily identical. You already knew this – you don’t get identical information from your mother and your father because they have different DNA (which gives them different traits). The different versions of one specific gene are known as alleles. As you learn about genetics, you will learn about how the information from both alleles of a specific gene interact to give an individual their trait. The genetic information that an individual has is called their genotype. The genotype of an individual produces the individual’s phenotype, or physical traits.

Figure 3. Meiosis. During meiosis, the DNA is copied once, then the cell divides twice. This produces cells with half as much genetic information as the original cell (1 copy of each chromosome). These cells become the sex cells (eggs or sperm). When two sex cells unite during fertilization, the original number of chromosomes (2 copies of each one) is restored (Photo credit: Wikimedia Commons).

Watch this great Amoeba Sisters video for a review of meiosis:

Section Summary

Genetics is the study of how traits are inherited from one generation to the next. Traits are variations in physical characteristics determined by proteins, which in term are determined by genes- segments of DNA that direct protein production. In eukaryotes, chromosomes carry genes, and each cell typically contains two copies of each nuclear chromosome, one from each parent. Organelles like mitochondria and chloroplasts have they own DNA, which is typically inherited from the maternal parent only. During meiosis, gametes (eggs and sperm) are produced, each containing one copy of each chromosome. When fertilization occurs, the offspring receive two copies of each gene. These copies may differ and are known as alleles. The genetic makeup of an individual is called their genotype, which influences their observable traits, or phenotype.

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Glossary

allele
Different versions of a gene that can exist at the same locus (position) on homologous chromosomes. Alleles can lead to different traits or characteristics.
diploid
A cell that contains two sets of chromosomes, one from each parent. Most cells in organisms, including humans, are diploid.
fertilization
The process in which a sperm cell and an egg cell join, combining their genetic material to form a zygote, which then develops into an offspring.
genotype
The genetic makeup of an individual, consisting of the alleles inherited from both parents. It determines the potential traits an individual can exhibit.
haploid
A cell that contains one complete set of chromosomes (half the number found in diploid cells). Gametes (sperm and egg cells) are haploid.
homologous
Chromosomes that are similar in size, shape, and genetic content, one inherited from each parent. They carry the same genes, though they may have different versions (alleles).
meiosis
A type of cell division that reduces the chromosome number by half, producing gametes (sperm and egg cells). It ensures genetic diversity and allows for sexual reproduction.
phenotype
The observable physical or biochemical characteristics of an individual, resulting from the interaction of their genotype and environmental factors.

References

Text adapted from OpenStax Biology 2e and used under a Creative Commons Attribution License 4.0.
Access for free at https://openstax.org/books/biology-2e/pages/1-introduction

Media Attributions

  • Overview-of-the-central-dogma-shows-the-flow-of-genetic-information-inside-a-biological
  • Amoeba sisters- deconstructed DNA
  • 66390_evo_resources_resource_image_175_original
  • Meiosis_Overview_new.svg

License

Icon for the Creative Commons Attribution-NonCommercial 4.0 International License

Concepts in Biology Copyright © by Christelle Sabatier; Michelle McCully; Dawn Hart; and Elizabeth Dahlhoff is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, except where otherwise noted.