BIO 181 Module 3 Exam Review

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30 Terms

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Central Dogma

tells the organization of genetic and protein structures

DNA → transcription → mRNA → translation → working proteins in ribosomes

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Pyrimidine bases

smaller molecules, single-ring

  • Cytosine (C)

  • Thymine (T)

  • Uracil (U) found in RNA


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Purine Bases

larger molecules, double-rings (pure as gold)

  • Guanine (G)

  • Adenine (A)


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Hydrogen Bonds

connect bases; rungs of the ladder

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Phosphodiester bonds

collect nucleotides; side rails of the ladder

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Chargaff’s Rules

Adenine (A) = Thymine (T)

Guanine (G) = Cytosine (C)

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5’

Phosphate end

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3’

Sugar end

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Antiparallel Strands

DNA strands run in opposite directions

One strand 5’ → 3’

Other strand 3’ → 5’

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How many chromosomes do humans have?

46

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Histone

folds and wraps around DNA to keep it organized

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Chromatin

extra condensed of double-helices; wraps around histones; condenses into chromosomes

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Which stage in the cell cycle is when DNA replication occurs?

Interphase

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Semi-Conservative DNA Replication

After replication

  • One old original strand is kept

  • One new synthesized strand is built


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DNA Replication Steps

  1. DNA is unzipped & the replication fork is formed

  2. RNA primer is formed

  3. DNA Polymerase III builds new complementary strands

  4. DNA Polymerase I replaces RNA primers

  5. Ligase combines Okazaki fragments


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Helicase

unwinds DNA by breaking hydrogen bonds

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Replication Fork

when DNA opens up and a Y-shaped structure forms

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Single-Strand Binding Proteins

bind to single strands and keep them apart (prevents re-zipping)

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Origin of Replication

sequence of bases that initiate unwinding

  • unzipping results in two template strands that will be “read” to form their complementary strands


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RNA Primer

short sequence of RNA that eventually allows DNA Polymerase to bind; starting point for DNA synthesis

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Primase

protein that lays the RNA primer down

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Leading strand

first base unzipped is on 3’

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Lagging strand

first base unzipped is on 5’

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DNA Polymerase III

builds new DNA/complementary strands on leading and lagging strands

  • reads 3’ to 5’

  • builds (synthesizes) 5’ to 3’


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On the leading strand

DNA polymerase binds the primers and adds complementary bases continuously

  • continuous, smooth, easy


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On the lagging strand

DNA polymerase binds the primers and adds complementary bases discontinuously

  • discontinuous, built in pieces (many Okazaki fragments)


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DNA Polymerase I

removes RNA primers and replaces them with deoxyribonucleotides (DNA)

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Ligase

(“glue”) joins Okazaki fragments; combines the sugar-phosphate backbone of the Okazaki fragments; seals sugar-phosphate backbone

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Exonuclease Activity

helps correct mistakes by extracting incorrect bases, however, some mistakes may still occur

  • proofreading ability of DNA polymerases that removes incorrectly paired nucleotides from a newly synthesized DNA strand


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