Heredity and Molecular Biology Lecture Review

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Comprehensive flashcards covering genetics, heredity, DNA molecular structure, protein synthesis, and cell division processes (Mitosis and Meiosis).

Last updated 9:06 PM on 5/20/26
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65 Terms

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Incomplete Dominance

A heterozygous phenotype is somewhere between the two homozygous parents, blending.

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Interphase

The portion of the cell cycle between two rounds of mitosis

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Prophase

First phase of mitosis, in which the replicated DNA condenses into chromosomes, the nuclear membrane begins to disintegrate, and spindle fibers begin to form

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Anaphase

Third phase of mitosis, in which the spindle fibers pull sister chromatids toward each end of the cell

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Metaphase

Chromosomes align along the equator of the cell

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Telophase

Fourth phase of mitosis, in which the spindle disappears and a nuclear membrane forms around each cluster of sister chromatids

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DNA polymerase

Enzyme that assembles individual nucleotides into a new complementary strand of DNA using a template

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RNA polymerase

Enzyme that transcribes DNA

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Codominance

Both alleles of a gene are expressed completely; neither is dominant or recessive.

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Trait

Distinguishing characteristics that are inherited from parent to offspring.

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Homologous chromosomes

Pairs of matching chromosomes.

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Autosomes

Chromosomes containing genes not directly related to the sex of an organism.

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Sex chromosomes

Chromosomes containing genes that control the development of sexual characteristics (XXXX female, XYXY male).

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Antigen

Protein markers on the surface of a red blood cell that determines the blood type of a person.

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Antibodies

Proteins made by the immune system that attack foreign antigens.

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Monohybrid Cross

Examines the inheritance of only ONE specific trait.

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Dihybrid Cross

Examines the inheritance of only TWO specific traits.

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Genotype

Genetic makeup, written with a combination of letters.

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Carrier

A person that holds the abnormal allele in their DNA; heterozygotes for a recessive trait who do not have the disease.

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Parental generation (P)

Pure bred, true-breeding parents (e.g., rr×RRrr \times RR).

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First filial generation (F1)

Offspring of the pure bred parents, which are always heterozygous (Rr×RrRr \times Rr).

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Second filial generation (F2)

Offspring of the F1 Generation.

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Phenotype

The observable physical expression of an organism’s genetic makeup written with descriptive words.

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Homozygous

When both chromosomes have identical alleles for a gene.

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Heterozygous

When chromosomes have two different alleles for a gene.

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Pedigree

A visual chart that depicts a family history or the transmission of a specific trait.

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Gametes

Sex cells (sperm, ovum) through which DNA is passed onto offspring.

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Punnett Square

A grid system for predicting all possible genotypes resulting from a cross.

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Karyotype

A picture of a person’s chromosomes organized by numbers.

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Allele

Alternative forms of a gene found at the same location on a chromosome.

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Universal donor

Type O blood, because it does not have any antigens.

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Universal recipient

Type AB blood, because it doesn’t have any antibodies.

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Chargaff

Discovered that the amount of adenine equals thymine (A=TA=T) and guanine equals cytosine (G=CG=C).

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Franklin

The scientist who took a picture of DNA.

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Wilkins

Suggested that DNA had a double helix structure.

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Nucleotide

The building block of nucleic acids consisting of a five-carbon sugar, one or more phosphate groups, and a nitrogenous base.

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Purine

A bulky nitrogenous base with a double ring, including guanine and adenine.

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Pyrimidine

A small nitrogenous base with a single ring, including thymine and cytosine.

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Central Dogma

The concept that DNA makes RNA, involving replication, transcription, and translation.

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Replication

The process occurring in the nucleus during the synthesis phase where DNA replicates using DNA helicase and DNA polymerase.

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Transcription

The first step of gene expression where genetic information from DNA is copied to produce a complementary strand of mRNA in the nucleus.

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Translation

The second step of gene expression occurring in the cytoplasm where mRNA is decoded by a ribosome to build a protein.

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Semiconservative

Using a parental strand to make a new one during DNA replication.

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Antiparallel

Refers to the two strands in DNA running in opposite directions (55' to 33' and 33' to 55').

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Okazaki fragments

Short pieces of DNA that make up the lagging strand, which is built in the opposite direction of the leading strand.

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Exons

An 'expressed' or protein-coding sequence that is retained during messenger RNA splicing.

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Introns

An 'intervening' sequence that is removed from an RNA molecule during splicing.

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Codon

A sequence of three nucleotides in mRNA that tells the ribosome where to start/end protein assembly and which amino acids to use.

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Anticodon

Three nucleotides in a transfer RNA (tRNA) molecule that pair specifically with a codon in mRNA.

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Point mutation

A permanent change in genetic makeup caused by the substitution of a single nucleotide for another.

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Interphase

The stage of the cell cycle where the cell replicates its DNA and organelles and grows; includes g1g1, SS, and g2g2 phases.

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Mitosis

The division of somatic cells in eukaryotic organisms producing two identical daughter cells.

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Cytokinesis

The division of the cytoplasm that occurs after telophase; not part of mitosis.

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Cleavage furrow

The structure that forms in animal cells during cytokinesis to pinch the cell in half.

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Cell plate

The structure that forms in plant cells during cytokinesis between the two daughter nuclei.

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Malignant tumor

A dangerous, fast-growing mass of cells able to break off and travel in the bloodstream.

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Metastasis

When cancer cells break off from a tumor and travel through the bloodstream to end up anywhere in the body.

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Cyclins and kinases

Proteins responsible for controlling the checkpoints within the cell cycle.

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Apoptosis

Programmed cell death essential for development and removing old or infected cells.

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Meiosis

The division of sex cells that involves two divisions and produces four genetically unique haploid daughter cells.

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Haploid cell (nn)

A cell containing one set of chromosomes (2323 in humans), typical of gametes.

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Diploid cell (2n2n)

A cell containing two sets of chromosomes (4646 in humans), typical of somatic cells.

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Crossing over

A process where homologous chromosomes break at identical locations and rejoin opposite partners during meiosis, mixing inherited genes.