The majority of Chromosomal DNA is non-coding and the location of genes are very important and affect the way they are passed on.
Here is a response from a geneticist, in point form:
1. Both autosome and sex chromosomes contain genes.
2. A gene is a strand of DNA, a fragment of chromosome
3. Not all of DNA on chromosome contains gene signals. A DNA sequence that
contains gene signals are called coding sequence or exon.
4. Usually, a coding sequence or exon for a gene is broken into several pieces by introns
(nonsense DNA ) on chromosome.
5. During transcription, the whole DNA strand for a gene is transcribed into mRNA. An editing process in cytoplasm removes the nonsense introns. The remaining mRNA will be translated into protein.
6. For diploid organism, there are two sets of DNA strands, or two alleles for a particular gene. Both alleles can be expressed (translated into protein).
7. Very often, we use the word gene for both DNA double strands (two alleles) and a specific allele. This may cause confusion.
Yes, a typical human autosome is diploid, meaning that each parent contributes one copy of each autosome to their offspring. This results in humans having two copies of each autosome, one from the mother and one from the father.
The diploid chromosome number in humans is 46.
A somatic cell with two of each type of chromosome has a diploid chromosome number. This means that the cell has a complete set of chromosomes, one from each parent.
Polyploidy is the condition in which a normally diploid cell or organism acquires one or more additional sets of chromosomes. In other words, the polyploid cell or organism has three or more times the haploid chromosome number. Polyploidy arises as the result of total nondisjunction of chromosomes during mitosis or meiosis.
A cellwith two of each kind of chromosomeis called a diploid cell and is said to contain a diploid, or 2n, number of chromosomes.
Yes, a typical human autosome is diploid, meaning that each parent contributes one copy of each autosome to their offspring. This results in humans having two copies of each autosome, one from the mother and one from the father.
The diploid chromosome number in humans is 46.
The condition in which a diploid cell is missing a chromosome or has an extra chromosome is called aneuploidy.
yes zygote do have diploid chromosome number
no
A diploid cell with an extra chromosome. Basically a diploid with an extra chromosome of one type, producing a chromosome number of the form 2n + l.
46
it has split in two
Haploid
It is fully diploid - chromosome configuration 2n -.
A somatic cell with two of each type of chromosome has a diploid chromosome number. This means that the cell has a complete set of chromosomes, one from each parent.
It is fully diploid - chromosome configuration 2n -.