how could a zygote end up with an extra chromosome
Either the egg or the sperm doesn't divide equally.
People end up with extra or missing chromosomes as a result of mistakes during meiosis. Meiosis is the process that creates sperm and egg cells (aka gametes). When meiosis works perfectly, sperm and egg cells get the correct number of chromosomes. Sometimes, however, meiosis doesn't work quite right, leading to sperm or egg cells that don't have the right number. When these sperm or egg cells lead to a new organism, then the entire organism won't have the number of chromosomes.
If the sperm or the egg don't divide equally. It's called fertilization when they join. The egg and the sperm come from two different organisms of the same species.
The cells do not divide =ly
Glencoe Science book
how could a zygote end up with an extra chromosome
Either the egg or the sperm doesn't divide equally.
A zygote could end up with an extra chromosome when during meiosis the sperm or the cell does not divide equally. This may make the zygote have 24 chromosomes instead of 23.
The normal cellular genetic complement number 2N is reduced to 1N in both of the sexual gametes so that when they recombine we end up with the standard chromosome number [1N + 1N = 2N] in our zygote.
Yes, it is!:)
A telomere is the structure at each end of a chromosome. It consists of an area of highly repeated DNA combined with protein. Its main function is to protect the end of the chromosome.Telomeres are instrumental in enabling the cells to divide and replicate. But as we grow older these tips wear out and shorten much like the shoelace caps. When they get too short, we get diseases and die. The three Nobel Prize winners found this as they were looking for a cure for cancer.
Describe the chromatic that make up a chromosome when a cell is ready to split
To simplify: the DNA molecule unzips and divides into 2 strands, then the replication makes the complements of each strand to make 2 full DNA daughter chromosomes, so half the parent DNA ends up in each daughter chromosome.
how could a zygote end up with an extra chromosome Either the egg or the sperm doesn't divide equally.
The normal cellular genetic complement number 2N is reduced to 1N in both of the sexual gametes so that when they recombine we end up with the standard chromosome number [1N + 1N = 2N] in our zygote.
You are born with it>>>>>>>>>>>During meiosis, chromosomes are separated equally. When they are notseparated equally - this is known as non-disjunction - the gametes end up with either an extra chromatid or no chromatid. In Down syndrome the offspring carries an extra chromatid in Chromosome 21, aka Trisomy 21
Klinefelter's syndrome occurs when an extra x chromosome shows up in a male or an extra y show up in a female. Principal effects include hypogonadism and sterility.
More males than females end up with sex-linked disorders because of the y chromosome. It is shorter than the x-chromosome, and increases susceptibility to these problems.
During meiosis, chromosomes are separated equally. When they are not separated equally - this is known as non-disjunction - the gametes end up with either an extra chromatid or no chromatid. In Down syndrome the offspring carries an extra chromatid in Chromosome 21, aka Trisomy 21.
aneuploidy usually reslts from non-disjunction (failure to separate) of homologous chromosomes during meiosis (the creation of gametes). It results in an organism having the wrong number of a certain chromosome. The two most common forms are monosomy (only one chromosme eg. Turner syndrome) and trisomy (three of a chromosome eg Down and Klinefelter syndrome) from non-disjunction, the two chromosomes line up at the equater of a cell as an X, ready to separate, but it doesn't, this reults in one egg/sperm having 0 of a chromosome and another will have 2. If the one with 0 then forms a zygote with a normal egg/sperm the zygote could have only 1 chromosome -from the normal egg/sperm. If the one with 2 forms a zygote the zygote will have 3 of the chromosome, 2 from the mutated gamtete and 1 from the normal gamete.
During meiosis, chromosomes are separated equally. When they are not separated equally - this is known as non-disjunction - the gametes end up with either an extra chromatid or no chromatid. In Down syndrome the offspring carries an extra chromatid in Chromosome 21, aka Trisomy 21.
Down syndrome happens by the splitting of the chromosomes. It is not a genetic disease. It is a chromosomaldisorder.Chromosomal changes like duplications or translocations1 occur in only one sex cell. A baby normally inherits 23 chromosomes from each parent to make a total of 46 chromosomes in 23 identifiable pairs.In Down Syndrome, an extra (duplicated) chromosome number 21 is inherited from either the father or the mother, to make a total of 47 chromosomes (23 pairs plus 1) in every cell of the DS child. (DS is also called Trisomy 21 ) DS is usually inherited from the mother, and the major risk of DS is the age of the woman at conception.1A duplication is an extra copy of a chromosome (or part of a chromosome) - a translocation is an extra bit of chromosome sticking onto another chromosome.
A chromosome is made up of many genes.
In the bladder, to be peed out.
A chromosome is made up of DNA, which has subunits called nucleotides.