DNA Replication & Transcription
Chromosomal Disorders
Translation
Mitosis & Meiosis
Mendel’s Laws
100

What is transcribed from DNA?

mRNA

100

What disorder is caused by trisomy 21?

Down syndrome

100

Where does translation occur?

Ribosome

100

How many daughter cells are produced in mitosis?

Two

100

Who is known as the father of genetics?

Gregor Mendel

200

Which enzyme unwinds the DNA double helix?

Helicase

200

What is Turner syndrome?

A disorder where females have only one X chromosome.

200

What molecule carries amino acids to the ribosome?

tRNA

200

How many daughter cells are produced in meiosis?

Four

200

What is the phenotypic ratio in a monohybrid cross Aa x Aa?

3:1

300

What is the role of primase in replication?

It synthesizes RNA primers

300

Which disorder is caused by an extra X chromosome in males?

Klinefelter syndrome

300

What is the start codon?

AUG

300

In which phase do homologous chromosomes separate?

Meiosis I

300

What is a genotype?

The combination of alleles an organism has

400

In eukaryotes, what modification occurs to pre-mRNA before it leaves the nucleus?

Splicing (removing introns) and adding a cap & poly-A tail

400

What is a karyotype?

A picture of an individual’s chromosomes.

400

What are codons?

Triplets of nucleotides that code for amino acids

400

What is the main difference between anaphase in mitosis and meiosis II?

Mitosis: sister chromatids separate; Meiosis II: sister chromatids separate again

400

What does the law of independent assortment state?

Alleles for different traits segregate independently.

500

Explain the difference between transcription in prokaryotes and eukaryotes.

Prokaryotes transcribe mRNA directly and it can be translated immediately; eukaryotes produce pre-mRNA that requires processing (splicing, 5’ cap, poly-A tail) before translation.

500

Explain how nondisjunction can lead to chromosomal disorders and give an example.

Nondisjunction is the failure of chromosomes to separate properly during meiosis, leading to an abnormal number of chromosomes (e.g., trisomy 21 → Down syndrome).

500

Describe the roles of the A, P, and E sites on the ribosome during translation.

A site = entry for tRNA; P site = holds tRNA with growing polypeptide; E site = exit site for empty tRNA.

500

Explain how crossing over contributes to genetic variation.

During prophase I of meiosis, homologous chromosomes exchange segments, creating new allele combinations in gametes.

500

What is a dihybrid cross and what phenotypic ratio is expected for a cross AaBb x AaBb?

A dihybrid cross studies two traits at once; expected phenotypic ratio = 9:3:3:1