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TEAS Science: DNA, Genes, and Inheritance Explained for Beginners

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Naxles TeamOctober 27, 2026
TEAS Science: DNA, Genes, and Inheritance Explained for Beginners

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Genetics is the study of heredity and variation in living organisms. For students preparing for the ATI TEAS exam, understanding DNA, genes, chromosomes, and inheritance provides a foundation for answering questions about cells and biological processes. These concepts may seem complicated at first, but learning how they relate to one another makes them easier to understand.

1. What is DNA?

DNA, or deoxyribonucleic acid, is the molecule that carries genetic information in living organisms. In human cells, most DNA is found in the nucleus. Some DNA is also present in mitochondria. DNA contains instructions that help cells function, develop, and produce proteins. Its structure resembles a twisted ladder called a double helix. The sides of this structure are made of sugar and phosphate groups, while the rungs contain paired nitrogenous bases. There are four DNA bases: adenine, thymine, cytosine, and guanine. Adenine pairs with thymine, while cytosine pairs with guanine. Understanding these basic relationships can help you answer introductory biology questions.

2. What are genes?

A gene is a segment of DNA that contributes to a functional product, such as a protein or functional RNA. Genes influence many characteristics of organisms. However, a trait is not always controlled by one gene alone. Many characteristics, including height, are influenced by multiple genes and environmental factors. For example, genetic information contributes to a person's potential height, while nutrition and health can also influence growth. When studying genetics, avoid assuming that every characteristic follows a simple pattern of inheritance.

3. Understand chromosomes

Chromosomes are structures made of DNA and associated proteins. They organize genetic information inside cells. Most human body cells contain 46 chromosomes arranged in 23 pairs. One chromosome in each pair generally comes from the biological mother and the other from the biological father. Human reproductive cells, such as sperm and eggs, normally contain 23 chromosomes each. During fertilization, these cells combine their genetic material to form a cell with 46 chromosomes. There are exceptions and variations, but these numbers provide a useful starting point for introductory biology.

4. Learn the difference between genotype and phenotype

A genotype describes an organism's genetic makeup in relation to a particular gene or set of genes. A phenotype refers to observable characteristics, such as certain physical traits or measurable biological features. Phenotype can result from the interaction of genotype with environmental conditions. In basic genetics examples, students may use letters to represent different versions of a gene. For instance, a classroom problem might use A and a to represent two alleles. Pay close attention to how the question defines the letters. Do not assume that a particular letter automatically represents a dominant or recessive allele without context.

5. Understand dominant and recessive inheritance

In a simplified Mendelian example, a dominant allele can influence a phenotype when only one copy is present, while a recessive phenotype may require two copies of a recessive allele. Suppose a hypothetical trait uses A for a dominant allele and a for a recessive allele. The genotypes AA and Aa would show the dominant phenotype in this simplified model, while aa would show the recessive phenotype. Real human traits are often more complicated. Some involve multiple genes, incomplete dominance, codominance, or other inheritance patterns. Use the model provided in a question rather than applying one pattern to every trait.

6. Practice reading genetic diagrams

Punnett squares help organize possible combinations of alleles from two parents. For example, if both parents have the genotype Aa, the possible combinations are: In this simplified model, the possible genotypes are one AA, two Aa, and one aa. The expected genotype ratio is 1:2:1. These proportions describe expected outcomes under the model, not guaranteed results for every family.

7. How to study genetics for the TEAS

Create a comparison chart for DNA, genes, chromosomes, genotype, and phenotype. Practice identifying each concept in short examples. Then work through basic inheritance questions and explain how each answer follows from the information given. Review incorrect answers carefully. If you confuse genes with chromosomes, revisit their definitions. If you struggle with Punnett squares, practice identifying the alleles each parent can contribute. A strong foundation in genetics can help you approach biology questions more confidently and connect individual concepts to the broader study of living organisms.

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