What the Cell
D2.1

Cell and nuclear division

HL extension
3 hours6 statementsTextbook pp. 662–669

Guiding questions

  1. How are large numbers of cells with identical genes produced?
  2. How do eukaryotes make genetically varied cells that can become gametes?

Slides

Slide 1 of 12

Notes

Written for this site from the class slides, with textbook page references for each statement. The chapter is on pages 662–669 of the course textbook. Image credits are on slide 12.

The cell cycle

D2.1.12

Cell proliferation

pp. 662–663

Cells proliferate for growth (plant meristems, early animal embryos), replacement (skin cells made in the basal layer replace those lost at the surface) and repair (healing a wound).

D2.1.13

Phases of the cell cycle

pp. 663–664

The cycle is interphase (G1, S and G2), then mitosis and cytokinesis. DNA is replicated in S. Some cells leave the cycle and stay in G0.

D2.1.14

Growth in interphase

pp. 664–665

Interphase is metabolically active: the cell makes proteins and membranes, replicates its DNA, and its mitochondria and chloroplasts grow and divide so each daughter cell receives enough.

D2.1.15

Cyclins

pp. 665–666
Slide: graph of four cyclins rising and falling through the cell cycle

Concentrations of different cyclins rise and fall during the cycle. Each activates a cyclin-dependent kinase, and a threshold level of a specific cyclin is needed to pass each checkpoint. The cyclin is then broken down.

Cancer

D2.1.16

Mutations in cell cycle genes

pp. 666–667

Proto-oncogenes stimulate division when signalled; a mutation can turn one into an oncogene that is always active (for example Ras). Tumour suppressor genes stop the cycle if DNA is damaged; mutations that inactivate both copies (for example p53) remove this brake. Either way, cells divide without control.

D2.1.17

Benign and malignant tumours

pp. 667–669

Benign tumours grow slowly and stay in one place; they are not cancer. Malignant tumours grow fast, invade nearby tissue and can metastasize: cells from the primary tumour travel in blood or lymph and form secondary tumours elsewhere.

Videos

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Note-taking sheet

Print this guide and complete it as you work through the slides and videos. It asks for your own explanations, so close the notes while you try each section.

First page of the note-taking sheet

Quick self-check

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Practice questions

A printable worksheet covering all six statements, from quick recall to data questions and a longer answer. It has 40 marks and takes about 40 minutes, or you can do one section at a time.

Your teacher has the mark scheme.

First page of the worksheet

Practical

Calculating a mitotic index

Lab40 minD2.1.13, D2.1.14

You will need: Prepared slide of root tip, or a micrograph, microscope, tally counter

  1. Find a field of view just behind the root tip
  2. Count the cells in mitosis and the total number of cells
  3. Calculate mitotic index
  4. Repeat in three fields, then discuss what a higher index in a tumour would suggest

Safety: Carry microscopes with two hands. Take care with glass slides.

Carry this out with your teacher's supervision and follow your school's lab rules.

Nature of science and TOK

Syllabus statements

Summarised in our own words. Use each code to find the exact wording in your textbook or the IB subject guide.

  • D2.1.12Cell proliferation for growth, replacement and repairp. 662
  • D2.1.13The stages of the cell cyclep. 664
  • D2.1.14How cells grow during interphasep. 665
  • D2.1.15How cyclins control the cell cyclep. 665
  • D2.1.16What happens when genes controlling the cell cycle mutatep. 667
  • D2.1.17How tumours differ in their division and growth rates, and in their ability to spread and invadep. 667

More of D2.1 in this course

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