big guns exam 4

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Last updated 4:16 AM on 11/17/25
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111 Terms

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Heredity

The passing of traits from parents to offspring.

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Genetics

The branch of biology that studies heredity and variation in organisms.

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Genetic variation

Differences in the genetic makeup among individuals within a population.

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Phenotype

The observable physical and physiological traits of an organism, determined by its genotype.

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Genotype

The genetic constitution of an organism.

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Gregor Mendel

The father of genetics known for his work on pea plants and the principles of inheritance.

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Hybrid

An organism that has two different alleles for a trait.

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True-breeding

Organisms that, when reproducing, create offspring identical to themselves.

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Parental generation (P)

The first individuals crossed in a breeding experiment.

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F1 generation

The first generation of offspring from a breeding cross.

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F2 generation

The second generation of offspring from a breeding cross.

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Blending inheritance

An outdated theory that offspring inherit a smooth blend of parental traits.

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Gene

A segment of DNA that codes for a specific trait.

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Allele

Different forms of a gene.

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Dominant

An allele that expresses its phenotype even in the presence of a recessive allele.

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Recessive

An allele that is only expressed in the phenotype if two copies are present.

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Principle of segregation

Mendel's principle stating that the two alleles for each trait separate during gamete formation.

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Punnett square

A diagram used to predict the outcome of genetic crosses.

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Locus (pl. loci)

The specific location of a gene on a chromosome.

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Homozygous

Having two identical alleles for a specific trait.

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Heterozygous

Having two different alleles for a specific trait.

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Monohybrid cross

A genetic cross that involves one trait.

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Phenotypic ratio

The ratio of different phenotypes in the offspring of a genetic cross.

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Dihybrid cross

A genetic cross that involves two traits.

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Principle of independent assortment

Mendel's principle that genes for different traits can segregate independently during the formation of gametes.

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Genetic recombination

The process of combining different DNA sequences to create genetic diversity.

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Linked genes

Genes that are located close together on the same chromosome and tend to be inherited together.

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Sex-linked genes

Genes located on sex chromosomes, often exhibiting unique inheritance patterns.

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Sex chromosomes

Chromosomes that determine the sex of an individual (X and Y in humans).

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Autosomes

Non-sex chromosomes that contain genes for traits unrelated to gender.

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Incomplete dominance

A genetic situation where one allele does not completely dominate another, resulting in a mixed phenotype.

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Codominance

A situation in which both alleles are expressed equally in the phenotype.

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Multiple alleles

More than two possible alleles exist for a single trait.

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Polygenic inheritance

Inheritance of traits that are controlled by multiple genes.

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DNA

The molecule that carries the genetic instructions for life.

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Gene

A segment of DNA that contains the instructions for the synthesis of proteins.

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Chromosome

A structure formed by condensed chromatin that contains genetic information.

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Histone

A protein that helps package DNA into a compact structure called chromatin.

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Nucleosome

A unit of DNA wrapped around a core of histone proteins.

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Cell Cycle

The series of events that lead to cell division and duplication.

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Interphase

The phase of the cell cycle where the cell spends most of its life, including G1, S, and G2 phases.

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Mitosis

The process of cell division that results in two identical daughter cells.

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Cytokinesis

The process that divides the cytoplasm of a parental cell into two daughter cells.

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Sister Chromatids

Identical copies of a chromosome, connected by a centromere.

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Centromere

The region of the chromosome that holds the two sister chromatids together.

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Asexual Reproduction

Reproduction that does not involve the fusion of gametes, resulting in clones.

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Homologous Chromosomes

Chromosome pairs, one from each parent, that are similar in shape, size, and genetic content.

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Diploid

A cell that contains two complete sets of chromosomes.

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Haploid

A cell that contains only one complete set of chromosomes.

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Meiosis

A type of cell division that produces gametes with half the number of chromosomes.

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Crossing-over

The exchange of genetic material between homologous chromosomes during meiosis.

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Genetic Recombination

The process of forming new combinations of alleles in offspring.

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Cleavage Furrow

The indentation that begins the process of cytokinesis in animal cells.

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Cell Plate

The structure that forms during cytokinesis in plant cells.

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Tetrad

A structure containing four chromatids formed during meiosis.

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Chiasma

The point at which paired chromosomes remain in contact during the crossing-over process.

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Interkinesis

The short resting period between the first and second meiotic divisions.

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DNA

Deoxyribonucleic acid, the molecule that carries genetic information.

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Double Helix

The structure of DNA, consisting of two strands wound around each other.

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Nucleotide

The basic structural unit of DNA, composed of a sugar, a phosphate group, and a nitrogenous base.

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Deoxyribose

The sugar component of DNA nucleotides.

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Purine

A type of nitrogenous base with a two-ring structure; includes adenine and guanine.

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Pyrimidine

A type of nitrogenous base with a single-ring structure; includes thymine and cytosine.

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Antiparallel

Describes the opposite orientation of the two strands of DNA.

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5’ end

The end of a DNA strand that has a phosphate group attached to the fifth carbon of the sugar.

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3’ end

The end of a DNA strand that has a hydroxyl group attached to the third carbon of the sugar.

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Chargaff’s rules

The observation that in DNA, the amount of adenine equals thymine and the amount of guanine equals cytosine.

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Semiconservative replication

The mode of DNA replication where each new DNA molecule consists of one old strand and one new strand.

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Origin of replication

The specific sequence of DNA where replication begins.

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Replication fork

The region where the DNA is split into two strands during replication.

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RNA (Ribonucleic acid)

A molecule involved in protein synthesis and sometimes in the replication process.

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RNA primer

A short strand of RNA that provides a starting point for DNA synthesis.

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Leading strand

The strand of DNA that is synthesized continuously in the same direction as the replication fork.

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Lagging strand

The strand of DNA that is synthesized discontinuously, in the opposite direction to the replication fork.

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Okazaki fragment

Short sequences of DNA synthesized on the lagging strand during DNA replication.

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Telomere

The protective end of a linear chromosome that prevents degradation.

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Helicase

An enzyme that unwinds the DNA double helix during replication.

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Primase

An enzyme that synthesizes RNA primers for DNA replication.

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DNA polymerase

An enzyme responsible for synthesizing new strands of DNA.

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Ligase

An enzyme that joins Okazaki fragments on the lagging strand.

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Telomerase

An enzyme that extends the telomeres of chromosomes.

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Transcription

The process of copying a segment of DNA into messenger RNA (mRNA).

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Translation

The process of converting the information in messenger RNA into a sequence of amino acids in a protein.

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Ribonucleic Acid (RNA)

A nucleic acid that plays a central role in the synthesis of proteins.

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Ribose

A sugar molecule that forms the backbone of RNA.

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Uracil

A nitrogenous base found in RNA that pairs with adenine.

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Messenger RNA (mRNA)

The type of RNA that carries the genetic information from DNA to the ribosome for protein synthesis.

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Transfer RNA (tRNA)

The type of RNA that transports specific amino acids to the ribosome during protein synthesis.

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Ribosomal RNA (rRNA)

A component of ribosomes that helps to catalyze protein synthesis.

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Promoter

A DNA sequence that initiates transcription of a particular gene.

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Template Strand

The strand of DNA that serves as the template for RNA synthesis.

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Antiparallel

Refers to the opposite orientation of the two strands of DNA or RNA.

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Codon

A sequence of three nucleotides that together form a unit of genetic code in a DNA or RNA molecule.

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Anticodon

A three-nucleotide sequence in tRNA that is complementary to a codon in mRNA.

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Ribosome

A cell structure that synthesizes proteins by translating mRNA into amino acids.

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A site

The site on the ribosome where the tRNA carrying the next amino acid binds.

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P site

The site on the ribosome where the tRNA holding the growing polypeptide chain is located.

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E site

The exit site on the ribosome where discharged tRNAs leave the ribosome.

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Peptide Bond

The chemical bond that links amino acids together in a protein.

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Mutation

A change in the nucleotide sequence of an organism's DNA.