Meiosis
DNA Structure
Protein Synthesis
Types of Mutations
Genetic Crosses
100

This process of cell division specifically produces gametes in humans.

meiosis

100

DNA stands for this

Deoxyribonucleic Acid

100

This type of RNA is responsible for carrying the genetic code from DNA to the cytoplasm.

mRNA (messenger RNA)

100

This type of mutation occurs when a single base pair in DNA is altered

point mutation

100

This term describes an organism with two identical alleles for a trait.

Homozygous
200

 During this stage of meiosis I, homologous chromosomes pair up at the equator of the cell.

metaphase I

200

These are the four bases found in DNA.

adenine, thymine, cytosine, and guanine

200

These small structures found in the cytoplasm read the RNA message to make proteins.

ribosomes

200

This mutation results from the addition or loss of DNA bases and changes the way the subsequent codons are read.

frameshift mutation

200

This tool is used to predict the result of a genetic cross. 

Punnett Square

300

This term describes the exchange of genetic material between non-sister chromatids during prophase I of meiosis.

crossing over

300
This is another name for the ladder portion (the sides) of DNA

sugar phosphate backbone

300

This is the process by which mRNA is decoded to produce a specific polypeptide according to the rules specified by the genetic code.

 translation

300

True or False: Mutations naturally occur

True

300

This type of genetic cross involves two traits where both parents are heterozygous for both traits, used to demonstrate independent assortment.

dihybrid cross

400

This number represents the total chromosomes in human gametes after meiosis, half of the total found in somatic cells.

23

400

This type of bond holds the nitrogenous bases together in the structure of DNA.

hydrogen bonds

400

Name the start codon for mRNA transcription in eukaryotes.

AUG

400

Name the mutation characterized by the presence of a base change that does not result in a different amino acid.

silent mutation

400

In this type of dominance, both alleles in the heterozygote are fully expressed, resulting in offspring with a phenotype that is neither dominant nor recessive.

codominance

500

This is the specific stage of meiosis I where homologous chromosomes separate and move to opposite poles.

anaphase I

500

This feature of DNA is responsible for its semi-conservative replication, where each strand serves as a template for a new one. (hint: how do you know what base matches with the template strand?) 

complementary base pairing rule

500

This term describes the sequence of three nucleotides in mRNA that does not code for an amino acid but instead signals the end of protein synthesis.  

stop codon

500

True or False: All mutations lead to change in proteins

False

500

This type of inheritance pattern is seen when a trait is controlled by multiple genes, each having a small additive effect on the phenotype.

This inheritance pattern is seen in traits such as eye color, height, and skin color

polygenic inheritance