Comprehensive Biology Review: DNA, Gene Expression, Cell Cycle, Meiosis, and Inheritance

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Vocabulary flashcards covering core topics in molecular biology, genetics, cell division, and inheritance patterns.

Last updated 2:57 AM on 10/7/26
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36 Terms

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Johannes Miescher

A scientist who first described DNA in 1869, identifying it as a substance rich in nitrogen and phosphorus rather than a protein.

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Transforming Principle

The phenomenon discovered by Frederick Griffith in which hereditary material is transferred from dead lethal S strain bacteria to live R strain bacteria.

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Avery and McCarty

Scientists who proved in 1940 that the transforming principle was DNA, demonstrating that DNA-degrading enzymes prevented transformation while RNA-degrading enzymes did not.

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Hershey and Chase

Researchers who established that bacteriophages inject DNA, not protein, into host bacteria to transmit hereditary information.

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Chargaff's Rules

Two principles stating that 1) adenine equals thymine (A=TA = T) and guanine equals cytosine (G=CG = C), and 2) DNA proportions of adenine and guanine differ between species.

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Nucleosome

A eukaryotic chromosome structural unit composed of a length of DNA wound twice around a histone spool.

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Semiconservative Replication

The mechanism of DNA replication yielding two double helices, each containing one original parental strand and one newly synthesized strand.

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Okazaki Fragments

Short segments of DNA synthesized discontinuously on the lagging strand that are subsequently joined together by DNA ligase.

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Somatic Cell Nuclear Transfer (SCNT)

A reproductive cloning technique where the nucleus of an unfertilized egg is replaced with a nucleus from a donor somatic cell.

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Transcription

The biological process of synthesizing an RNA strand using a gene's DNA sequence as a template.

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Alternative Splicing

A post-transcriptional RNA modification in eukaryotes where exons are rearranged into different combinations to produce distinct mRNA transcripts.

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Codon

A sequence of three nucleotides in mRNA that specifies a particular amino acid or a termination signal during translation.

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AUG

The start codon in mRNA that initiates translation and specifies the amino acid methionine.

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Frameshift Mutation

A mutation caused by nucleotide insertion or deletion that shifts the genetic reading frame and drastically alters the resulting protein.

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Ribosome-Inactivating Proteins (RIPs)

Toxins, such as ricin, that completely halt cellular protein synthesis by removing adenine bases from rRNA.

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Interphase

The main cell cycle interval consisting of G1G_1, SS, and G2G_2 stages, during which the cell grows, replicates DNA, and prepares for division.

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Mitosis

A nuclear division process in eukaryotic cells that preserves the chromosome number in descendant cells.

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Contractile Ring

A ring of actin filaments that forms during animal cell cytokinesis to pull the plasma membrane inward and divide the cytoplasm.

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Cell Plate

A disk-shaped structure formed by fusing vesicles at the division plane during plant cell cytokinesis, eventually developing into a new cell wall.

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Telomeres

Noncoding, repetitive DNA sequences located at the ends of eukaryotic chromosomes that shield essential genetic information from degradation.

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Telomerase

An enzyme found in stem cells and cancer cells that reverses telomere shortening to grant cellular immortality.

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Oncogene

A mutated proto-oncogene that drives uncontrolled cell division and transforms a normal cell into a tumor cell.

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HeLa Cells

An immortal human cell line derived in 1951 from cervical cancer patient Henrietta Lacks, extensively used in global medical research.

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Meiosis

A nuclear division process in eukaryotes that reduces the chromosome number from diploid (2n2n) to haploid (nn) to form gametes.

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Red Queen Hypothesis

An evolutionary theory stating that species must continually adapt and evolve to survive against co-evolving competitors and changing environments.

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Crossing Over

The exchange of genetic segments between nonsister chromatids of homologous chromosomes during prophase I of meiosis.

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Chromosome Segregation

The random distribution of maternal and paternal homologous chromosomes during meiosis I, generating 2232^{23} possible combinations in human gametes.

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Bdelloid Rotifers

Microscopic asexual animals that have survived for 80 million years without sex by acquiring roughly 10% of their active genes from bacteria, fungi, and plants.

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Law of Segregation

Mendel's principle that homologous chromosomes separate during meiosis so that each gamete carries only one allele for each gene.

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Law of Independent Assortment

Mendel's principle that allele pairs for different genes on nonhomologous chromosomes distribute into gametes independently of one another.

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Incomplete Dominance

An inheritance pattern in which the phenotype of a heterozygote is an intermediate blend of the two homozygous phenotypes.

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Codominance

An inheritance pattern where both alleles in a heterozygote are fully and simultaneously expressed, as seen in human ABO blood types.

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Epistasis

A genetic interaction where one gene masks or modifies the phenotypic expression of an entirely different gene.

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Pleiotropy

A genetic pattern where a single gene impacts multiple, seemingly unrelated phenotypic characteristics.

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Continuous Variation

A spectrum of minor phenotypic differences in a population for a trait influenced by multiple genes and environmental conditions.

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F508\text{F508} Mutation

A 3-base pair deletion in the CFTR gene that removes the 508th amino acid, causing thick mucus accumulation in individuals with cystic fibrosis.