How do you use a Punnett square?

A Punnett square is a simple grid used to predict the possible genetic outcomes of a cross between two parents. Think of it like a multiplication table for biology, where you match up the traits from each parent to see what combinations their offspring might inherit. <br><br> To use it, you write the genotype (the letter combinations representing genes) of one parent across the top and the other down the left side. Then, you fill in the empty boxes by combining the row and column letters. The resulting grid shows you all the possible genetic combinations and helps you calculate the probability of each trait appearing in the next generation.

What are alleles?

Before drawing the square, you need to understand alleles. Alleles are different versions of a gene. We represent them with letters. A capital letter stands for a dominant allele, which means it will mask the other version. A lowercase letter stands for a recessive allele, which only shows up if there is no dominant allele present. For example, if TT is tall and tt is short, a plant with TtTt will be tall.

Setting up the grid

Start by drawing a two-by-two grid for a single-trait cross (a monohybrid cross). Take the genotype of parent one and write its two letters above the two columns. Take the genotype of parent two and write its two letters beside the two rows. Since each parent passes on only one allele per gene to their offspring, separating the letters this way represents the sex cells (sperm and egg) carrying those individual alleles.

Filling in the boxes

To fill out the square, simply bring the top letters down into the boxes below them, and bring the side letters across into the boxes next to them. Each box inside the grid will end up with two letters, representing the genotype of a potential offspring. By convention, if a box gets a capital letter and a lowercase letter, you always write the capital letter first (like AaAa, not aAaA).

Reading the results

Once the grid is full, count the different types of genotypes inside the four boxes. Each box represents a 25% chance of that specific outcome. If two boxes have the genotype AaAa and two have aaaa, there is a 50% chance the offspring will be AaAa and a 50% chance they will be aaaa. Remember to distinguish between genotype (the letters) and phenotype (the physical trait you actually see).

Worked through

Cross a heterozygous tall pea plant (TtTt) with a homozygous short pea plant (tttt). What is the probability that their offspring will be short?

First, identify the parents: Parent 1 is TtTt and Parent 2 is tttt. Draw a 2x2 grid. Put the TT and tt of Parent 1 over the two columns. Put the tt and tt of Parent 2 next to the two rows. Now fill in the boxes. The top row of boxes gets a tt from the side; combined with the top, they become TtTt and tttt. The bottom row also gets a tt from the side, resulting in TtTt and tttt. Out of the four boxes, two contain TtTt (tall) and two contain tttt (short). Therefore, there are 2 out of 4 chances to get a short plant. The probability of the offspring being short is 50%.

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Where this comes from: OpenStax Biology 2e, Chapter 12: Mendel's Experiments and Heredity · Khan Academy, High School Biology: Classical Genetics

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