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When chromosome pairs fail to separate aneuploidy occurs due to non-disjunction. This can result in monosomy or trisomy of the chromosome. These are mistakes made in chromosome segregation during meiosis. If pairs of homologous chromosomes fail to separate during the first meiotic division or if the centromere joining sister chromatids fails to separate during the second meiotic division, gametes, and hence offspring, will be produced that have too many and too few chromosomes.
If this occurs in a cell of the body that is undergoing mitosis, the body will destroy the cell. If it occurs in a gametic cell (ovum or sperm) then the result can be trisomy, which is when the offspring receives three of the same chromosome rather than the normal two. Often the embryo will abort itself if this occurs but if you end up with three copies of chromosome 21 this is known as Down syndrome. One the creation of a cell with trisomy, another cell results that is missing the chromsome so it is possible to end up with gametes missing a chromosome aswell, which will usuallr cause the embryo to abort, or may lead to serious defects in the offspring
The tetrads (pairs of homologous chomosomes) split up during Anaphase I in Meiosis I.

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Related Questions

What process separates chromosome?

Mitosis and Meiosis


What will separate in the first division in meiosis one?

Homologous chromosomes will separate in the first division of meiosis 1, moving to opposite poles of the cell in a process called disjunction. This results in the reduction of the chromosome number by half.


When chromosomes separate what is the process called?

The process of chromosomes separating during cell division is called "chromosome segregation" or "chromosome disjunction." This ensures that each new cell receives the correct number of chromosomes.


Do genes on the same chromosome separate?

Genes on the same chromosome can separate through a process called genetic recombination or crossing over during meiosis. This process can shuffle genes between homologous chromosomes, creating genetic diversity in offspring.


How does nondisjunction cause Trisomy 21?

Nondisjunction is a process during cell division where chromosomes fail to separate correctly. In Trisomy 21, an individual has three copies of chromosome 21 instead of the usual two, which is caused by nondisjunction during either meiosis I or meiosis II in the formation of gametes. When a gamete with an extra copy of chromosome 21 is fertilized, it results in an individual with Down syndrome.


How is the chromosome number halved during which specific process in the cell cycle?

The chromosome number is halved during the process of meiosis in the cell cycle.


What is the Chromosome number is reduced by a process called?

The chromosome number is reduced by a process called meiosis. Meiosis is a specialized cell division process that results in the formation of gametes (sperm and egg cells) with half the number of chromosomes as the parent cell.


Does. The chromosome number change in meiosis?

No it doesnt change. The chromosomes will stay at the same number unless there is a mutation through the process of meiosis.


Can autosomes go through meiosis?

Yes, autosomes are any chromosome that is not a sex chromosome, and they do go through meiosis. During meiosis, autosomes are involved in the process of genetic recombination and independent assortment, which help generate genetic diversity.


The process of meiosis never results in the formation of a?

The process of meiosis never results in the formation of a Diploid.


Which process occurs when chromosomes do no separate during meiosis?

nondijunction


How does the process of segregation occur in meiosis, specifically with homologous pairs separating to opposite poles?

During meiosis, segregation occurs when homologous pairs of chromosomes separate and move to opposite poles during the first division of meiosis. This process ensures that each resulting gamete receives only one copy of each chromosome, leading to genetic diversity in offspring.