The Central Dogma of Molecular Biology and Cell Cycle

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Vocabulary practice flashcards covering DNA structure, transcription, translation, replication, mutations, and the cell cycle based on lecture slides.

60 Terms

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Central Dogma of Molecular Biology

The core framework describing the flow of genetic information in a biological system from DNA to RNA and protein.

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Major Groove

A structural region of the DNA double helix that exposes nucleotides and facilitates the binding of transcription factors, polymerases, and nucleases.

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Minor Groove

A structural region of the DNA double helix that binds antibiotics and dyes or stains.

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Law of Complementary Base Pairing

A lock and key principle in DNA and RNA where a purine binds a specific pyrimidine through hydrogen bonding.

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Antiparallel Strands

Strands of DNA running in opposite directions (5′→3′5' \rightarrow 3' and 3′→5′3' \rightarrow 5'), named based on the carbon atoms on the sugar backbone.

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Chromatin

A complex of DNA, protein, and RNA that PACKAGES DNA into a small volume, REINFORCE DNA for mitosis, PREVENTS DNA damage, and CONTROLS gene expression.

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Nucleosome

A fundamental unit of chromatin structure consisting of DNA wrapped around a protein octamer composed of histones.

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Enhancer

A distal DNA regulatory element that binds activator proteins to stimulate chromatin remodeling and initiate transcription.

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Promoter Region

A DNA sequence that binds RNA Polymerase and contains a TATA box (TATAAA\text{TATAAA}) where DNA unwinding occurs.

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Exon

A sequence of DNA that is retained in mature pre-mRNA and eventually becomes part of a functional protein.

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Intron

A non-coding sequence of DNA that is excised from the primary transcript during RNA processing.

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<p>Decondensed Chromatin</p>

Decondensed Chromatin

An open state of chromatin required for transcription to occur, promoted by DNA demethylation, histone acetylation by HATs, and histone demethylation.

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Mediator

A protein complex bound by activators that triggers the assembly of RNA Polymerase and general transcription factors at the promoter site.

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<p>Template Strand</p>

Template Strand

The 3′→5′3' \rightarrow 5' DNA strand read by RNA Polymerase during transcription elongation.

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Coding Strand

The 5′→3′5' \rightarrow 3' DNA strand that shares the same sequence as the pre-mRNA transcript, except with thymine instead of uracil.

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Pyrophosphate (PPi\text{PP}_i)

A byproduct released during synthesis reactions when nucleotide triphosphates (NTPs) are incorporated into RNA.

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Poly-A Signal Sequence

A specific sequence that directs RNA Polymerase to terminate transcription and detach from the DNA molecule.

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5' Cap and Poly-A Tail

Structural additions made to RNA during processing that regulate nuclear export, prevent degradation, and promote translation.

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Alternative Splicing

A regulatory mechanism that allows a single gene to code for multiple proteins by selectively including or excluding different exons in mRNA.

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Ribosome

A complex composed of protein and ribosomal RNA that acts as a ribozyme to form peptide bonds during translation, featuring A, P, and E binding sites.

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<p>Transfer RNA (tRNA)</p>

Transfer RNA (tRNA)

An RNA molecule carrying a specific amino acid and featuring an anticodon that hydrogen bonds to an mRNA codon.

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<p>Triplet Codon</p>

Triplet Codon

A three-nucleotide sequence in mRNA or tRNA that specifies a single amino acid.

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Degeneracy

The property of the genetic code in which multiple distinct triplet codons code for the same amino acid.

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<p>Cap-Dependent Translation Initiation</p>

Cap-Dependent Translation Initiation

Translation initiation involving a 43S43\text{S} pre-initiation complex scanning the mRNA from the 5′5' cap to locate the AUG start codon.

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Cap-Independent Translation Initiation

Translation initiation where protein complexes bind directly to the start site without scanning, typically occurring under cellular stress.

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P Site (Peptidyl Site)

The ribosomal site initially occupied by initiator tRNA bound to methionine during translation initiation.

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A Site (Aminoacyl Site)

The ribosomal site where a new incoming aminoacyl-tRNA enters to pair with the mRNA codon.

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E Site (Exit Site)

The ribosomal site where uncharged tRNAs relocate before exiting the ribosome.

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<p>Peptide Bond</p>

Peptide Bond

A chemical bond formed between amino acids via a dehydration synthesis reaction releasing H2O\text{H}_2\text{O}.

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<p>Termination Factor</p>

Termination Factor

A protein (such as eRF1) that binds to a stop codon at the ribosome's A site, leading to the release of the protein and dissociation of RNA.

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<p>Post-Translational Modification (PTM)</p>

Post-Translational Modification (PTM)

Covalent structural additions to proteins after synthesis, such as acetylation, methylation, phosphorylation, sulfation, and glycosylation.

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Replication Origins

AT-rich DNA regions where replication starts, forming replication bubbles with forks at both ends.

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Origin Recognition Complex (ORC)

A hexameric protein complex that recognizes and binds the replication origin during pre-replication complex assembly.

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Minichromosome Maintenance Complex (MCM)

A complex with helicase activity responsible for unwinding DNA during replication.

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<p>Replisome</p>

Replisome

A molecular machine at each replication fork containing MCMs, GINS, Cdc45, and DNA Polymerases.

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Leading Strand

The newly synthesized DNA strand that is synthesized continuously in the 5′→3′5' \rightarrow 3' direction toward the replication fork.

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<p>Lagging Strand</p>

Lagging Strand

The newly synthesized DNA strand synthesized discontinuously in Okazaki fragments away from the replication fork.

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Primase

An enzyme that lays down short RNA primers needed for DNA Polymerase to begin synthesis on the lagging strand.

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<p>Telomerase</p>

Telomerase

An enzyme containing an RNA template that adds repetitive sequences to chromosome ends to fill gaps left by lagging strand replication.

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<p>Germline Mutation</p>

Germline Mutation

A genetic mutation occurring in gametes that can be passed on to offspring and affects all cells of the organism.

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Somatic Mutation

A genetic mutation occurring in non-germline body cells that affects only the individual and is not inherited by offspring.

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Spontaneous Mutation

A genetic alteration that arises naturally due to uncorrected errors during normal DNA replication.

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Induced Mutation

A genetic alteration caused by exposure to external environmental mutagens, such as radiation or chemical agents.

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Insertion Mutation

A type of mutation resulting from the addition of one or more base pairs into a DNA sequence.

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Deletion Mutation

A type of mutation resulting from the removal of one or more base pairs from a DNA sequence.

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G1 Phase (Gap 1)

The cell cycle phase where the cell accumulates materials for replication, doubles organelles, and carries out primary growth and metabolism.

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G0 Phase (Resting Phase)

A state entered by faulty or terminally differentiated cells that permanently or temporarily cease division.

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S Phase (Synthesis Phase)

The stage of interphase during which nuclear DNA is replicated and centrioles are duplicated.

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G2 Phase (Gap 2)

The stage of interphase where centriole duplication completes and cell division control proteins are produced.

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<p>M Phase (Mitosis)</p>

M Phase (Mitosis)

The cell cycle phase during which nuclear division and cytokinesis divide a cell into two identical daughter cells.

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<p>Cell Cycle Checkpoints</p>

Cell Cycle Checkpoints

Surveillance mechanisms (G1, S, G2, and M) that halt cell cycle progression if DNA damage or incomplete replication/assembly is detected.

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Cyclin and Cyclin-Dependent Kinase (CDK)

Protein complexes that regulate key steps of the cell cycle, including replication initiation in G1, preventing re-replication in S, and M phase entry in G2.

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Prophase

The initial mitotic stage where chromatin condenses into chromosomes, centrosomes move apart, and the mitotic spindle forms.

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Metaphase

The mitotic stage where sister chromatids align along the metaphase plate in the middle of the cell.

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Anaphase

The mitotic stage where sister chromatids separate and are pulled to opposite spindle poles.

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Telophase

The final stage of nuclear division where nuclear membranes reform, chromosomes decondense, and spindle fibers disassemble.

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Cytokinesis

The division of the cell cytoplasm into two separate daughter cells following nuclear division.

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<p>Kinetochore</p>

Kinetochore

A protein structure located on the centromere of each chromosome that serves as the attachment point for spindle microtubules.

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<p>Anaphase Promoting Complex (APC)</p>

Anaphase Promoting Complex (APC)

A protein complex activated during metaphase when microtubules are attached to kinetochores, triggering sister chromatid separation.

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Contractile Ring

A ring of actin and myosin filaments that pinches the cell membrane inward to create the cleavage furrow during cytokinesis.