AP BIOLOGY

THE MOLECULAR BASIS OF INHERITANCE

GENE MUTATION

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
A piece of a chromosome is copied and remains within the chromosome
A
deletion
B
duplication
C
inversion
D
translocation
Explanation: 

Detailed explanation-1: -Duplications. Duplications occur when part of a chromosome is abnormally copied (duplicated). This type of chromosomal change results in extra copies of genetic material from the duplicated segment.

Detailed explanation-2: -A chromatid is one of the two identical halves of a chromosome that has been replicated in preparation for cell division. The two “sister” chromatids are joined at a constricted region of the chromosome called the centromere.

Detailed explanation-3: -The term “duplication” simply means that a part of a chromosome is duplicated, or present in 2 copies. This results in having extra genetic material, even though the total number of chromosomes is usually normal.

Detailed explanation-4: -In chromosomal duplications, extra copies of a chromosomal region are formed, resulting in different copy numbers of genes within that area of the chromosome.

Detailed explanation-5: -Duplication Duplication, as related to genomics, refers to a type of mutation in which one or more copies of a DNA segment (which can be as small as a few bases or as large as a major chromosomal region) is produced. Duplications occur in all organisms.

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