Translocation in the study of DNA involves the synthesis of proteins from ribosome structures. It starts when the mRNA leaves the nucleus (end of transcirption) and moves to the cytoplasm. From there a tRNA molecule carrying the corresponding amino acid for each codon on the mRNA forms the corresponding chain of proteins. This process continues until all of the codons on the mRNA are read by the tRNA. Each time a protein is bound to the tail end of the mRNA, an amino acid is added to the end of the link. By the end, a long chain of proteins has been constructed, based on the original DNA blueprint for that particular protein to be built.
in shorter terms, a chromosome piece breaks off and reattaches to a non-homologous chromosome
Translocations are the transfer of a piece of one chromosome to a non-homologous chromosome. They are often reciprocal, with the two chromosomes swapping segments with each other. In most cases of chronic myelogenous leukaemia (CML), the leukaemic cells share a chromosomal abnormality known as Philadelphia chromosome. This abnormality is the result of a reciprocal translocation between chromosomes 9 and 22. An abnormal hybrid gene is created leading to the production of a novel protein that is not normally found in the cell. This protein prevents normal growth and development, leading to leukaemia.
from wikipedia.
In reference to genetics, translocation means moving a part of a chromosome to a different location within that chromosome or to an entirely different chromosome. This can result in an abnormality of the chromosome.
When a gene breaks off from it's sequence and goes to another one or "relocates"
Translocations mutations occur in chromosomes, wherein chromosome segments change positions. It can either take place within a chromosome or between chromosomes.
a translocation mutated chromosome example below:
A B C D E + 1 2 3 4 5 → A B C D 4 5 + 1 2
chromosomal mutation
translocation .. this is wrong.its a point mutation :)
This condition is referred to as chromosomal translocation.
Translocation. On Chromosome 20.
structural mutation have four types of change in the chromosomal structure: TRANSLOCATION, INVERSION, DELETION AND DUPLICATION.while:numerical mutation results from nondisjunction, or the failure of a pair of homologous choromosomes or a pair of sister chromatids to separate during meiosis or mitosis. The effect of nondisjunction during mitosis is not harmful as the effect of nondisjunction during meiosis.
No that occurs all the time through translocation. It is not a mutation.
chromosomal mutation
translocation .. this is wrong.its a point mutation :)
This condition is referred to as chromosomal translocation.
translocation
chromosomal Translocation
A very small number.
Translocation. On Chromosome 20.
When part of one chromosome breaks off and attaches to another.
when there is a two way exchange of genetic portion between two non-homologus chromosomes, its called reciprocal mutation, its a type of translocation mutation
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
translocation
structural mutation have four types of change in the chromosomal structure: TRANSLOCATION, INVERSION, DELETION AND DUPLICATION.while:numerical mutation results from nondisjunction, or the failure of a pair of homologous choromosomes or a pair of sister chromatids to separate during meiosis or mitosis. The effect of nondisjunction during mitosis is not harmful as the effect of nondisjunction during meiosis.