Cell Signaling
Cell Tissue and Architecture
Replication
Mitosis, Cell Cycle Regulation
Mutations
100

In this type of local signaling, growth factors and cytokines act on nearby cells in the same tissue.

Paracrine signaling

100

Made of long chains of protein subunits, this cellular framework provides internal structural support and enables movement of substances within the cell.

the cytoskeleton

100

DNA polymerase can only add nucleotides to this specific end of a growing strand, which is why all new DNA strands are synthesized in the 5′→3′ direction.

the free 3' end

100

Where are the checkpoints located in the cell cycle

G1, G2, M

100

This type of point mutation is a single-base substitution that changes one codon so that a different amino acid is incorporated into the protein, as in sickle-cell disease.

missense mutation

200

In hormonal signaling, hormones may reach almost all body cells, but only these cells recognize and respond to a given hormone.

target cells

200

These two cytoskeletal polymers are polar, growing more quickly at their plus ends than their minus ends; in animal cells, one of them is anchored with its minus ends at the centrosome and plus ends projecting toward the cell membrane. Name both.

microtubules and microfilaments

200

At the replication fork, this enzyme relieves the overwinding strain caused by helicase ahead of the fork, preventing the DNA from becoming too tightly coiled.

topoisomerase

200

what is the order of mitosis?

PMAT!

200

In this kind of substitution, a codon is changed into a stop codon (UAA, UAG, or UGA), truncating the protein, whereas in this other kind of substitution, the codon changes but still specifies the same amino acid, leaving the protein sequence unchanged.

nonsense and silent mutation

300

In this stage of signaling, the message is passed along inside the cell via intermediate steps, often amplifying the signal.

Signal transduction

300

For a carcinoma cell to become metastatic via the bloodstream, it must cross this specialized extracellular matrix layer that underlies blood vessels twice, and it often uses specific integrins to do so.

the basal lamina

300

At a replication origin, the two parental strands separate to create a structure that contains two active sites where new DNA is being synthesized in opposite directions. Name this overall structure and the specific sites where synthesis is occurring.

a replication bubble with two replication forks

300

what is the difference between G0 and apoptosis

G0 is a holding phase for premature genes, and apoptosis is regulated cell death

300

This class of mutation is caused by the insertion or deletion of one or two nucleotides, shifting the reading frame from the point of change onward, usually making all downstream amino acids wrong and often introducing a premature stop—especially severe when it occurs near the 5′ end of the gene.

frameshift mutation

400

Name two types of cellular responses to a signal (must be biological and not moving your hand off of a stove)

gene expression, growth factors, exocytosis, cell replication, apoptosis

400

Label the cytoskeletal elements from thinnest to thickest

microfilaments, intermediate filaments, microtubules

400

why is telomerase a unique enzyme and what is it's function in our body?

it extends DNA ends without requiring a DNA template (it uses its own built-in template)

400

draw and label every part of the cell cycle

g1, S, g2, prophase, metaphase, anaphase, telophase, 

400

Because the genetic code is read in non-overlapping triplets, inserting or deleting nucleotides near this end of the coding sequence tends to produce the most severe protein defects.

near the 5' end 

500

Draw and label every part of a traditional signal transduction pathway

should include ligand, GPCR, G protein, an enzyme, second messenger (activated), and a cell response
500

Name every adherins junction and describe their function

tight junctions: connect cells to cell in a tight seal (no liquid passes through)

gap junctions: form pores from cell to cell to allow small molecules to flow across 

desmosomes: connect cell to cell using intermediate filaments

hemidesmosomes: connect cell to matrix using intermediate filaments

500

Draw and label a DNA strand unwinding and being replicated (including Okazaki fragments and leading strand)

bonus points if you discussed enzymes involved!

500

Describe the function of each step of the cell cycle

  • G₁ phase (Gap 1): The cell grows, makes proteins and organelles, and checks whether conditions are good enough to start DNA replication.

  • S phase (Synthesis): The cell accurately replicates its DNA so each chromosome becomes two identical sister chromatids.

  • G₂ phase (Gap 2): The cell continues to grow, produces proteins needed for mitosis, and checks that all DNA has been correctly replicated and repaired.

  • M phase (Mitosis + Cytokinesis): The duplicated chromosomes are separated into two nuclei and the cell splits into two genetically identical daughter cells.

  • G₀ phase (Resting state): The cell exits the cycle and remains metabolically active but does not actively divide.

500

decribe each type of mutation we dicussed in lecture


  • Point mutation: Any small-scale mutation that changes one or a few nucleotides in the DNA sequence.

  • Substitution mutation: A point mutation where one nucleotide base is replaced by another.

  • Missense mutation: A substitution that changes a codon so a different amino acid is incorporated into the protein.

  • Nonsense mutation: A substitution that converts a codon into a stop codon (UAA, UGA, or UAG), causing premature termination of the protein.

  • Silent mutation: A substitution that changes a nucleotide but does not change the amino acid sequence of the protein.

  • Frameshift mutation: An insertion or deletion of 1 or 2 bases that shifts the reading frame, usually scrambling all amino acids downstream and often introducing a premature stop.

  • Deletion mutation: A mutation where nucleotides are removed; deleting 1–2 bases causes a frameshift, while deleting sets of 3 bases removes one or more amino acids without shifting the reading frame.



M
e
n
u