AP BIOLOGY

THE MOLECULAR BASIS OF INHERITANCE

GENE MUTATION

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
A chromosome fails to separate from its homologue during meiosis
A
translocation
B
nondisjunction
C
point mutation
D
substitution
Explanation: 

Detailed explanation-1: -In nondisjunction, the separation fails to occur causing both sister chromatids or homologous chromosomes to be pulled to one pole of the cell. Mitotic nondisjunction can occur due to the inactivation of either topoisomerase II, condensin, or separase.

Detailed explanation-2: -Nondisjunction means that a pair of homologous chromosomes has failed to separate or segregate at anaphase so that both chromosomes of the pair pass to the same daughter cell. This probably occurs most commonly in meiosis, but it may occur in mitosis to produce a mosaic individual.

Detailed explanation-3: -If homologous chromosomes fail to separate during meiosis I, the result is two gametes that lack that particular chromosome and two gametes with two copies of the chromosome.

Detailed explanation-4: -Nondisjunction occurs when chromosomes fail to segregate during meiosis; when this happens, gametes with an abnormal number of chromosomes are produced. The clinical significance is high: nondisjunction is the leading cause of pregnancy loss and birth defects.

Detailed explanation-5: -Nondisjunction is the failure of homologous chromosomes to disjoin correctly during meiosis. This results in the production of gametes containing a greater or lesser chromosomal amount than normal ones. Consequently the individual may develop a trisomal or monosomal syndrome.

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