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Patterns of Inheritance

Chromosome mutations and genetic counselling

  • 3 things to know
  • Components 01, 02 and 03

Overview

Recall questions on chromosome and gene mutations, non-disjunction and translocation, Down's syndrome and maternal age, Turner's and Klinefelter's syndromes, reading pedigrees for recessive and X-linked conditions, prenatal tests, and the ethics and non-directive nature of genetic counselling.

What you need to know

Answer each one before you reveal it.

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Key term

What does a genetic counsellor do?

Key term

How does a chromosome mutation differ from a gene mutation?

Key term

What is non-disjunction?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    How does a chromosome mutation differ from a gene mutation?

    Model answer

    A gene mutation changes the base sequence within a single gene, whereas a chromosome mutation changes the number or the structure of whole chromosomes.

  2. 2

    What is non-disjunction?

    Model answer

    Non-disjunction is the failure of homologous chromosomes to separate in meiosis I, or of sister chromatids to separate in meiosis II, so a gamete gains an extra chromosome or lacks one.

  3. 3

    What is a chromosome translocation?

    Model answer

    A translocation is a chromosome mutation in which a section of one chromosome breaks off and becomes attached to a different, non-homologous chromosome.

  4. 4

    State the chromosome complement of a person with Down's syndrome caused by non-disjunction.

    Model answer

    They have 47 chromosomes, with three copies of chromosome 21 instead of the usual two.

  5. 5

    How can Down's syndrome arise in a person who has 46 chromosomes?

    Model answer

    Most of an extra chromosome 21 can be attached to another chromosome by a translocation, so the count is still 46 but the chromosome 21 material is present in triplicate.

  6. 6

    Why does the risk of a Down's syndrome pregnancy rise with the age of the mother?

    Model answer

    Oocytes are arrested part-way through meiosis I from before birth, so the longer they stay arrested the more likely the homologous chromosomes are to fail to separate when meiosis is completed.

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