Genetics and Molecular Biology: DNA, Genes, and Regulation

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Last updated 1:22 AM on 3/25/26
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82 Terms

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microfilaments are cytoskeletal elements that can be which of the following? Choose

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Genome

The complete set of DNA in a cell or organism including coding and noncoding sequences

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Gene

A segment of DNA that is expressed to yield a functional product either RNA or a protein

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Coding gene

A gene that produces mRNA which is translated into a protein

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Non-coding gene

A gene that produces a functional RNA that is not translated into a protein such as rRNA or tRNA

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5′ UTR

A region at the beginning of mRNA that is not translated but regulates translation

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3′ UTR

A region at the end of mRNA that is not translated and regulates mRNA stability

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Introns

Non-coding sequences within a gene that are transcribed but removed during RNA processing

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Exons

Expressed sequences that remain in mRNA and may code for protein

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Non-transcribed spacer

DNA between genes that is not transcribed into RNA

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Transcribed spacer

RNA sequences that are transcribed but later removed and degraded and are not spliced like introns

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Primary RNA transcript (pre-mRNA)

The initial RNA transcript containing both introns and exons

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Mature mRNA

The processed RNA after introns are removed and exons are joined

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Start codon

AUG signals the start of translation and beginning of the coding region

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Stop codon

A codon that signals the end of translation

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Iron Response Element (IRE)

A regulatory RNA sequence that binds iron regulatory proteins to control gene expression based on iron levels

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Ferritin

A protein that stores iron inside cells

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Ferritin IRE location

The IRE is located in the 5′ UTR of ferritin mRNA

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Ferritin regulation low iron

IRPs bind the IRE in the 5′ UTR and block translation so ferritin is not produced

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Ferritin regulation high iron

IRPs do not bind allowing translation and production of ferritin to store iron

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Transferrin receptor

A protein that helps cells import iron from the bloodstream

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Transferrin receptor IRE location

The IREs are located in the 3′ UTR of transferrin receptor mRNA

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Transferrin receptor regulation low iron

IRPs bind the IREs in the 3′ UTR stabilizing mRNA and increasing receptor production

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Transferrin receptor regulation high iron

IRPs do not bind leading to mRNA degradation and decreased receptor production

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5′ UTR regulation effect

Binding of proteins in the 5′ UTR blocks or allows translation initiation

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3′ UTR regulation effect

Binding of proteins in the 3′ UTR affects mRNA stability and degradation

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Opposite regulation principle

Ferritin and transferrin receptor are regulated oppositely to balance iron storage and uptake

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Genome size vs complexity

Genome size does not directly correlate with organism complexity

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Repetitive DNA

DNA sequences that are repeated many times and make up a large portion of the genome

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Gene families

Groups of related genes formed by duplication that have similar but distinct functions

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Alternative splicing

A process where one gene can produce multiple proteins by including or excluding exons

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Chromatin

DNA packaged with proteins mainly histones to organize and compact it in the nucleus

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Histones

Positively charged proteins that bind negatively charged DNA to help package it

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DNA replication

The process by which DNA makes an identical copy of itself to pass genetic information to the next generation

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Function of genome

To maintain and transfer genetic information and to use that information for cellular activities

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DNA polymerase

An enzyme that synthesizes new DNA by adding nucleotides to the 3′ hydroxyl of a growing strand

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Direction of DNA synthesis

New DNA is synthesized in the 5′ to 3′ direction

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Template reading direction

DNA polymerase reads the template strand in the 3′ to 5′ direction

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Substrates of DNA replication

Deoxyribonucleotides and a template strand with a primer

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Primer

A short RNA strand that provides a free 3′ hydroxyl group for DNA polymerase to begin synthesis

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Primase

An RNA polymerase that synthesizes RNA primers de novo for DNA replication

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De novo synthesis

Synthesis from scratch without a pre-existing strand

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Origin of replication

A specific location where DNA replication begins

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Replication fork

A Y-shaped region where DNA strands are separated and replication occurs

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Replication bubble

A region where DNA is being replicated in both directions from an origin

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Leading strand

The DNA strand synthesized continuously in the same direction as the replication fork

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Lagging strand

The DNA strand synthesized discontinuously in the opposite direction of the replication fork

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Okazaki fragments

Short DNA fragments synthesized on the lagging strand

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DNA ligase

An enzyme that joins Okazaki fragments by forming phosphodiester bonds

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Helicase

An enzyme that unwinds the DNA double helix by breaking hydrogen bonds

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Single-strand binding proteins

Proteins that stabilize separated DNA strands and prevent reannealing

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Topoisomerase

An enzyme that relieves supercoiling by cutting and rejoining DNA strands

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Sliding clamp

A protein that holds DNA polymerase onto the DNA template to increase efficiency

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Clamp loading protein

A protein that loads the sliding clamp onto DNA

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DNA polymerase III

The main enzyme responsible for DNA synthesis in prokaryotes

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DNA polymerase I

An enzyme that removes RNA primers and replaces them with DNA

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RNase H

An enzyme that removes RNA from RNA-DNA hybrids

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Multiple origins of replication

Eukaryotic chromosomes have many origins to allow faster replication of large genomes

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Circular vs linear DNA

Prokaryotes have circular DNA while eukaryotes have linear DNA

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End replication problem

The inability to fully replicate the ends of linear DNA after removal of RNA primers

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Telomeres

Repetitive DNA sequences at the ends of chromosomes that protect genetic information

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Telomerase

An enzyme that extends telomeres using an RNA template

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Reverse transcriptase

An enzyme that synthesizes DNA from an RNA template

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DNA replication fidelity

The accuracy of DNA replication maintained through multiple mechanisms

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Complementary base pairing

Correct nucleotide pairing increases replication accuracy

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Proofreading activity

DNA polymerase removes incorrect nucleotides using 3′ to 5′ exonuclease activity

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Mutation

A change in DNA sequence that can be spontaneous or induced

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Spontaneous mutation

A mutation caused by natural chemical changes such as deamination or depurination

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Induced mutation

A mutation caused by external agents such as UV light or chemicals

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Thymine dimers

Covalent bonds between adjacent thymine bases caused by UV radiation

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Alkylating agents

Chemicals that modify DNA bases and can cause mutations

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Direct repair

A mechanism that reverses DNA damage without removing bases

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Photolyase

An enzyme that uses light energy to break thymine dimers

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Suicide enzyme

An enzyme that permanently modifies itself during repair and cannot be reused

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Base excision repair

A process that removes damaged bases and replaces them with correct nucleotides

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DNA glycosylase

An enzyme that removes a damaged base from DNA

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AP site

A site in DNA where the base has been removed

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AP endonuclease

An enzyme that cuts the DNA backbone at an AP site

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DNA polymerase and ligase role in repair

They fill in missing nucleotides and seal the DNA backbone

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Gene editing

A method to repair DNA by targeting specific sequences

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Zinc finger nucleases

Engineered proteins that cut DNA at specific sequences

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CRISPR

A gene editing system that uses guide RNA to target specific DNA sequences

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