bio cell cycle and DNA replication

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Last updated 7:41 PM on 4/18/26
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44 Terms

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cell cycle

The series of events a cell goes through to grow and divide.

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Interphase

Includes G1, S, and G2

Cell grows, copies DNA, and prepares for division

Longest part of the cell cycle

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G1 Phase (Gap 1)

Cell grows in size

Produces proteins and organelles

Normal cell functions occur

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S Phase (Synthesis)

DNA is replicated

Each chromosome is copied → forms sister chromatids

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G2 Phase (Gap 2

Further growth

Cell prepares for mitosis

Checks DNA for errors

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Mitosis (M Phase)

Division of nucleus

Sister chromatids separate into two nuclei

Followed by cytokinesis (cell splits into 2 cells)

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Sister Chromatids =

Two identical copies of a chromosome attached together.

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When are sister chromatids made?

During S phase of interphase

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Relationship to original chromosome

They are identical copies of the original DNA molecule

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How many strands in each chromatid?

Each chromatid = 1 double helix (2 strands of DNA)

DNA is always double-stranded

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Orientation of DNA strands

Strands are antiparallel

One runs 5’ → 3’

Other runs 3’ → 5’

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5’ end

Has a phosphate group attached to the 5’ carbon

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3’ end

Has a hydroxyl (-OH) group on the 3’ carbon

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Each new DNA molecule contains:

1 original (parent) strand

1 new strand

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Direction of synthesis

New DNA is made 5’ → 3’

Template is read 3’ → 5’

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Base pairing rules guide replication:

A pairs with T

C pairs with G

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Where are sister chromatids held together?

At the centromere

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Enzyme that uncoils DNA

Helicase

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Opening strands

Helicase breaks hydrogen bonds between bases

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stabilizing proteins

Single-strand binding proteins (SSBs)

Prevent strands from rejoining or tangling

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Role of primase

Lays down RNA primers

Needed because DNA polymerase cannot start on its own

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DNA polymerase III (main enzyme)

Adds nucleotides 5’ → 3’

Uses base-pairing rules

Proofreading:

3’ → 5’ exonuclease activity

Removes incorrect bases

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Template:

3’ → 5’ (left → right)

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New strand:

5’ → 3’ (left → right)

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Leading strand =

continuous synthesis

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Lagging strand =

discontinuous (Okazaki fragments)

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Leading strand

Continuous

Fewer primers

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Lagging strand

Made in fragments

Requires more primase activity

Because it must restart repeatedly

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Second polymerase

DNA polymerase I

Has 5’ → 3’ exonuclease activity

Removes RNA primers and replaces them with DNA

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Final enzyme

DNA ligase

Seals gaps between fragments

More gaps on the lagging strand

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Eukaryotes note

Same process, different enzymes

Example: DNA polymerase delta

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Circular Chromosome

One origin of replication

Replication moves in two directions (bidirectional)

Forms a replication “bubble”

Ends meet → complete circle

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Linear Chromosome

Multiple origins of replication

More complex

Ends (telomeres) require special handling

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