AP BIOLOGY

HEREDITY

MUTATIONS

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
Translocation ____
A
involves two nonhomologous chromosomes, part of one breaks off and is transferred to the other.
B
occurs when a piece of chromosome is lost or removed.
C
is when a chromosome breaks off, then the segment flips and reattaches.
D
occurs when a gene sequence is repeated.
Explanation: 

Detailed explanation-1: -In a translocation, a segment from one chromosome is transferred to a nonhomologous chromosome or to a new site on the same chromosome. Translocations place genes in new linkage relationships and generate chromosomes without normal pairing partners.

Detailed explanation-2: -Reciprocal translocation is a chromosome abnormality caused by exchange of parts between non-homologous chromosomes. Two detached fragments of two different chromosomes are switched.

Detailed explanation-3: -A translocation, as related to genetics, occurs when a chromosome breaks and the (typically two) fragmented pieces re-attach to different chromosomes. The detection of chromosomal translocations can be important for the diagnosis of certain genetic diseases and disorders.

Detailed explanation-4: -Reciprocal translocations are a transfer of genetic material between homologous chromosomes. These are most commonly balanced exchanges, such that no genetic material is lost and individuals are phenotypically normal.

There is 1 question to complete.