Biology 9700 · AS & A Level · Passage of information from parents to offspring
Passage of information from parents to offspring — practice question
At times during meiosis, homologous chromosomes do not separate at anaphase; this is called non-disjunction. Turner’s syndrome is the most common chromosome mutation in females. It may arise because non-disjunction occurs in meiosis during gametogenesis. Some of the gametes formed will therefore lack an X chromosome.
In some cases of Turner’s syndrome, one of the pair of X chromosomes is not absent but has been damaged. The damaged X chromosome may have broken and then rejoined so that part of its structure is lost.
Fig. 7.1 shows a normal X chromosome and two types of ‘damaged’ X chromosomes, $X_1$ and $X_2$:
• In $X_1$, part of the ‘p’ arm of the chromosome is absent. This deletion causes reduced height in the female and defects such as narrowing of the aorta.
• In $X_2$, part of the ‘q’ arm of the chromosome is absent. This deletion causes little or no development of the ovaries.
(a)[1]
Name the structure K.
(b)[2]
Explain how $X_1$ and $X_2$ produce different phenotypes.
(c)[4]
Mothers with the $X_1$ form of Turner’s syndrome can pass the chromosome mutation to their daughters but not to their sons.
Complete the genetic diagram below to show how chromosome mutation $X_1$ may be passed to daughters from a mother with Turner’s syndrome.
Worked solution & mark scheme
This 7-mark question has a full step-by-step worked solution and mark scheme. One marking point: “the centromere” …